Study of Niraparib, TSR-022, Bevacizumab, & Platinum-Based NCT03307785

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number	NCT03307785
Other study ID #	213351
Secondary ID	3000-01-002
Status	Active, not recruiting
Phase	Phase 1
First received
Last updated
Start date	October 12, 2017
Est. completion date	April 22, 2024

Study information
Verified date	February 2024
Source	Tesaro, Inc.
Contact	n/a
Is FDA regulated	No
Health authority
Study type	Interventional

Clinical Trial Summary

Part A: To test the safety and tolerability of combination therapy with Niraparib and TSR-042 and to establish a safe dose that will be used in a Phase 2 study. Part B: To test the safety and tolerability of combination therapy with Carboplatin-Paclitaxel and TSR-042 and to establish a safe dose that will be used in a Phase 2 study. Part C: To test the safety and tolerability of combination therapy with Niraparib, TSR-042 and Bevacizumab and to establish a safe dose that will be used in a Phase 2 study. Part D: To test the safety and tolerability of combination therapy with Carboplatin-Paclitaxel, TSR-042 and Bevacizumab and to establish a safe dose that will be used in a Phase 2 study. Part E: To test the safety and tolerability of combination therapy with Carboplatin-Pemetrexed and TSR-042 and to establish a safe dose that will be used in a Phase 2 study. Part F: To test the safety and tolerability of combination therapy with Carboplatin-Pemetrexed, TSR-022 and TSR-042 and to establish a safe dose that will be used in a Phase 2 study. Part G: To test the safety and tolerability of combination therapy with Carboplatin-nab-Paclitaxel, TSR-042 and to establish a safe dose that will be used in a Phase 2 study. Part H: To test the safety and tolerability of combination therapy with Carboplatin-nab-Paclitaxel, TSR-022 and TSR-042 and to establish a safe dose that will be used in a Phase 2 study. Part I: To test the safety and tolerability of combination therapy with Carboplatin-Paclitaxel, TSR-022 and TSR-042 and to establish a safe dose that will be used in a Phase 2 study.

Recruitment information / eligibility
Status	Active, not recruiting
Enrollment	58
Est. completion date	April 22, 2024
Est. primary completion date	February 26, 2020
Accepts healthy volunteers	No
Gender	All
Age group	18 Years and older
Eligibility	Inclusion Criteria: - Patient has histologically or cytologically proven advanced (unresectable) or metastatic cancer as outlined below according to study part and disease type: - Part A: Patients with previously treated advanced or metastatic cancer. Patient may have received no more than 4 lines of treatment for advanced or metastatic cancer. Hormonal treatment will not be considered a prior line of treatment. - Part B: Patients with advanced or metastatic cancer for which treatment with carboplatin-paclitaxel is considered appropriate therapy. Patient may have received no more than 1 prior line of chemotherapy in the metastatic setting. Hormonal treatment will not be considered a prior line of treatment. - Part C: Patients with previously treated advanced or metastatic cancer. Patient may have received no more than 4 lines of treatment for advanced or metastatic cancer. Hormonal treatment will not be considered a prior line of treatment. - Part D: Patients in whom carboplatin-paclitaxel and bevacizumab is considered appropriate therapy. Patient may have received no more than 1 prior line of chemotherapy in the metastatic setting. Hormonal treatment will not be considered a prior line of treatment. - Part E and F: Patients who have not received prior systemic therapy, including targeted therapy and biologic agents, for their advanced or metastatic (Stage = IIIB or IV) Non-Squamous NSCLC. Patients who have received neoadjuvant or adjuvant therapy are eligible as long as development of advanced or metastatic disease occurred at least 12 months after completion of neoadjuvant or adjuvant therapy. - Part G, H, and I: Patients who have not received prior systemic therapy, including targeted therapy and biologic agents, for their advanced or metastatic (Stage = IIIB or IV) NSCLC. Patients who have received neoadjuvant or adjuvant therapy are eligible as long as development of advanced or metastatic disease occurred at least 12 months after completion of neoadjuvant or adjuvant therapy. - Patient has an Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1. - Patient has adequate organ function. - Female patient has a negative serum pregnancy test within 72 hours prior to taking study treatment if of childbearing potential and agrees to abstain from activities that could result in pregnancy from screening through 180 days after the last dose of study treatment, or is of non-childbearing potential. - Male patient agrees to use an adequate method of contraception and not donate sperm starting with the first dose of study treatment through 90 days after the last dose of study treatment. Note: Abstinence is acceptable if this is the established and preferred contraception for the patient. - Patient has measurable lesions by RECIST v1.1. For Part A and C, in addition to the general inclusion criteria, patients must also meet the following additional criterion to be considered eligible to participate in this study: - Patient is able to take oral medications. - For patients to be eligible for any parts of the study using niraparib 300 mg as a starting dose, a screening actual body weight = 77 kg and screening platelet count = 150,000 u/L is necessary. Exclusion Criteria: (Patients will not be eligible for the study entry if any of the following criteria are met) - Patient has known active central nervous system metastases, carcinomatous meningitis, or both. - Patient has a known additional malignancy that progressed or required active treatment within the last 2 years. Exceptions include basal cell carcinoma of the skin, squamous cell carcinoma of the skin that has undergone potentially curative therapy, or in situ cervical cancer. - Patient is considered a poor medical risk due to a serious, uncontrolled medical disorder, nonmalignant systemic disease, or active infection that requires systemic therapy. - Patient has a condition (such as transfusion-dependent anemia or thrombocytopenia), therapy, or laboratory abnormality that might confound the study results or interfere with the patient's participation - Patient is pregnant or expecting to conceive children within the projected duration of the study, starting with the screening visit through 180 days after the last dose of study treatment. Note: No data are available regarding the presence of niraparib or its metabolites in human milk, or on its effects on the breastfed infant or milk production. Because of the potential for serious adverse reactions in breastfed infants from niraparib, female patients should not breastfeed during treatment with niraparib and for 1 month after receiving the final dose. - Patient has a known history of human immunodeficiency virus (type 1 or 2 antibodies). - Patient has known active hepatitis B or hepatitis C. - Patient has an active autoimmune disease that has required systemic treatment in the past 2 years. - Patient has received prior therapy with an anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CTLA-4 including ipilimumab), or any other antibody or drug specifically targeting T-cell co-stimulation or checkpoint pathways. - Patient has undergone prior treatment with a known PARP inhibitor. - Known history or current diagnosis of MDS or AML. - Patient has a known hypersensitivity to TSR-042 components or excipients. For Parts B, D, E, F, G, H, and I, patients will not be eligible for study entry if any of the following additional exclusion criterion are met: • Patient has a known hypersensitivity to any of the following relevant study treatments: carboplatin, paclitaxel, pemetrexed, nab-paclitaxel, or TSR-022 components or excipients. For Parts C and D only, patients will not be eligible for study entry if the following additional exclusion criterion is met: - Patient has clinically significant cardiovascular disease (e.g., significant cardiac conduction abnormalities, uncontrolled hypertension, myocardial infarction, cardiac arrhythmia or unstable angina, New York Heart Association Grade 2 or greater congestive heart failure, serious cardiac arrhythmia requiring medication, Grade 2 or greater peripheral vascular disease, and history of cerebrovascular accident [CVA]) within 6 months of enrollment. - Patient has a history of bowel obstruction, including subocclusive disease, related to the underlying disease and history of abdominal fistula, gastrointestinal perforation, or intra abdominal abscesses. Evidence of recto-sigmoid involvement by pelvic examination or bowel involvement on CT scan or clinical symptoms of bowel obstruction. - Patient has proteinuria as demonstrated by urine protein: creatinine ratio =1.0 at screening or urine dipstick for proteinuria =2 (patients discovered to have =2 proteinuria on dipstick at baseline should undergo 24-hour urine collection and must demonstrate <2 g of protein in 24 hours to be eligible). - Patient is at increased bleeding risk due to concurrent conditions (e.g., major injuries or surgery within the past 28 days prior to start of study treatment, history of hemorrhagic stroke, transient ischemic attack, subarachnoid hemorrhage, or clinically significant hemorrhage within the past 3 months). - Patient has a known hypersensitivity to bevacizumab components or excipients. For Parts E and F only, patients will not be eligible for study entry if any of the following additional exclusion criteria are met: - Patient is unable to interrupt aspirin or other nonsteroidal ant-inflammatory drugs, other than an aspirin dose = 1.3 g per day, for a 5-day period (8-day period for long -acting agents, such as piroxicam. - Patient is unable or unwilling to take folic acid, vitamin B12 supplement. - Patient has symptomatic ascites or pleural effusion. A patient who is clinically stable following treatment for these conditions (including therapeutic thoraco- or paracentesis) is eligible. For Parts G, H, and I only, patients will not be eligible for study entry if any of the following additional exclusion criteria are met: • Patient has pre-existing peripheral neuropathy that is Grade = 2 by Common Terminology Criteria for Adverse Events (CTCAE) version 4 criteria. For Parts E, F, G, H and I only, patients will not be eligible for study entry if any of the following additional exclusion criteria are met: • Patient has interstitial lung disease or a history of pneumonitis that required oral or intravenous glucocorticoids to assist with management.

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Niraparib
Niraparib is a potent, orally active PARP1 and PARP2 inhibitor being developed as a treatment for patients with tumors that harbor defects in the homologous recombination DNA repair pathway or that are driven by PARP-mediated transcription factors.
• TSR-042
TSR-042 is a humanized monoclonal antibody that binds with high affinity to PD-1 resulting in inhibition of binding to programmed death receptor ligands 1 and 2 (PD-L1 and PD-L2).
• Carboplatin-Paclitaxel
Carboplatin in combination with paclitaxel is a chemotherapy treatment that has been shown to be efficacious against a variety of different tumor types, including non-small cell lung cancer [NSCLC], ovarian cancer, endometrial cancer, and head and neck cancer.
• Bevacizumab
Bevacizumab is a chemotherapy treatment that has been shown to be efficacious against a variety of different cancer types, including colon cancer, lung cancer, glioblastoma, and renal-cell carcinoma. Bevacizumab is in the angiogenesis inhibitor and monoclonal antibody families of medication. It works by slowing the growth of new blood vessels.
• TSR-022
TSR-022 is a monoclonal antibody against TIM-3 (also called HAVCR2), an immune checkpoint receptor. Immune checkpoint proteins are molecules that help to regulate the immune system so it does not mistakenly attack healthy cells. However, they can also keep immune cells from recognizing and killing cancer cells. TIM-3 is found on the surface of certain T-cells, including tumor-infiltrating T-cells, that have left the bloodstream and migrated into the tumor environment. By binding to and blocking TIM-3, TRS-022 allows for T-cells to become activated so as to enhance T-cell-mediated attacks on tumors. These attacks reduce their growth.
• Carboplatin-Pemetrexed
Pemetrexed and platinum therapy in combination with pembrolizumab (anti-PD-1 antibody) has proven to be efficacious in a first line setting for nonsquamous NSCLC patients
• Carboplatin-Nab-Paclitaxel
Nab-paclitaxel is a formulation of paclitaxel that is indicated for locally advanced or metastatic NSCLC, as first-line treatment in combination with carboplatin in patients who are not candidates for curative surgery or radiation therapy. Nab-paclitaxel has shown increased ORR and time to progression in metastatic breast cancer compared with solvent-based paclitaxel and has shown antitumor activity and improved ORR compared with solvent-based paclitaxel as first-line therapy in patients with NSCLC.

Locations
Country	Name	City	State
United States	GSK Investigational Site	Canton	Ohio
United States	GSK Investigational Site	Cleveland	Ohio
United States	GSK Investigational Site	Encinitas	California
United States	GSK Investigational Site	Houston	Texas
United States	GSK Investigational Site	Nashville	Tennessee
United States	GSK Investigational Site	San Marcos	Texas
United States	GSK Investigational Site	Sarasota	Florida
United States	GSK Investigational Site	Scottsdale	Arizona

Sponsors *(1)*
Lead Sponsor	Collaborator
Tesaro, Inc.

Country where clinical trial is conducted

United States,

References & Publications (1)

Yap TA, Bessudo A, Hamilton E, Sachdev J, Patel MR, Rodon J, Evilevitch L, Duncan M, Guo W, Kumar S, Lu S, Dezube BJ, Gabrail N. IOLite: phase 1b trial of doublet/triplet combinations of dostarlimab with niraparib, carboplatin-paclitaxel, with or without bevacizumab in patients with advanced cancer. J Immunother Cancer. 2022 Mar;10(3):e003924. doi: 10.1136/jitc-2021-003924. — View Citation

Outcome
Type	Measure	Description	Time frame
Primary	Part A: Number of Participants With Dose-limiting Toxicity (DLT)	An event was considered a DLT if it occurred within the first 21 days of treatment, and met one of following DLT criteria:hematologic toxicity- Grade4 thrombocytopenia persists for >=7 days from the time of adverse event(AE) onset, Grade 4 neutropenia, Grade 4 or Grade 3 febrile neutropenia persists for >=7 days, Grade4 or Grade3 anemia requiring blood transfusion, Grade 3 thrombocytopenia associated with clinically significant bleeding, Grade 3 neutropenia associated with infection as described in Common Terminology Criteria for Adverse Events (CTCAE) version 4.0, drug related Grade 3 or 4 non-hematologic toxicity, drug related Grade 3 or 4 nonhematologic laboratory abnormality if any of the following also occur: abnormality leads to hospitalization and abnormality persists for >=7 days from the time of AE onset; drug related toxicity leading to prolonged delay (>2 weeks) in initiating Cycle 2. DLTs were collected during first cycle to establish recommended phase 2 dose (RP2D).	21 days
Primary	Part B: Number of Participants With DLT	An event was considered a DLT if it occurred within the first 21 days of treatment, and met one of following DLT criteria:hematologic toxicity- Grade4 thrombocytopenia persists for >=7 days from the time of AE onset, Grade 4 neutropenia, Grade 4 or Grade 3 febrile neutropenia persists for >=7 days, Grade4 or Grade3 anemia requiring blood transfusion, Grade 3 thrombocytopenia associated with clinically significant bleeding, Grade 3 neutropenia associated with infection as described in CTCAE version 4.0, drug related Grade 3 or 4 non-hematologic toxicity, drug related Grade 3 or 4 nonhematologic laboratory abnormality if any of the following also occur: abnormality leads to hospitalization and abnormality persists for >=7 days from the time of AE onset; drug related toxicity leading to prolonged delay (>2 weeks) in initiating Cycle 2. DLTs were collected during first cycle to establish RP2D.	21 days
Primary	Part C: Number of Participants With DLT	An event was considered a DLT if it occurred within the first 21 days of treatment, and met one of following DLT criteria:hematologic toxicity- Grade4 thrombocytopenia persists for >=7 days from the time of AE onset, Grade 4 neutropenia, Grade 4 or Grade 3 febrile neutropenia persists for >=7 days, Grade4 or Grade3 anemia requiring blood transfusion, Grade 3 thrombocytopenia associated with clinically significant bleeding, Grade 3 neutropenia associated with infection as described in CTCAE version 4.0, drug related Grade 3 or 4 non-hematologic toxicity, drug related Grade 3 or 4 nonhematologic laboratory abnormality if any of the following also occur: abnormality leads to hospitalization and abnormality persists for >=7 days from the time of AE onset; drug related toxicity leading to prolonged delay (>2 weeks) in initiating Cycle 2. DLTs were collected during first cycle to establish RP2D.	21 days
Primary	Part D: Number of Participants With DLT	An event was considered a DLT if it occurred within the first 21 days of treatment, and met one of following DLT criteria:hematologic toxicity- Grade4 thrombocytopenia persists for >=7 days from the time of AE onset, Grade 4 neutropenia, Grade 4 or Grade 3 febrile neutropenia persists for >=7 days, Grade4 or Grade3 anemia requiring blood transfusion, Grade 3 thrombocytopenia associated with clinically significant bleeding, Grade 3 neutropenia associated with infection as described in CTCAE version 4.0, drug related Grade 3 or 4 non-hematologic toxicity, drug related Grade 3 or 4 nonhematologic laboratory abnormality if any of the following also occur: abnormality leads to hospitalization and abnormality persists for >=7 days from the time of AE onset; drug related toxicity leading to prolonged delay (>2 weeks) in initiating Cycle 2. DLTs were collected during first cycle to establish RP2D.	21 days
Primary	Part E: Number of Participants With DLT	An event was considered a DLT if it occurred within the first 21 days of treatment, and met one of following DLT criteria:hematologic toxicity- Grade4 thrombocytopenia persists for >=7 days from the time of AE onset, Grade 4 neutropenia, Grade 4 or Grade 3 febrile neutropenia persists for >=7 days, Grade4 or Grade3 anemia requiring blood transfusion, Grade 3 thrombocytopenia associated with clinically significant bleeding, Grade 3 neutropenia associated with infection as described in CTCAE version 4.0, drug related Grade 3 or 4 non-hematologic toxicity, drug related Grade 3 or 4 nonhematologic laboratory abnormality if any of the following also occur: abnormality leads to hospitalization and abnormality persists for >=7 days from the time of AE onset; drug related toxicity leading to prolonged delay (>2 weeks) in initiating Cycle 2. DLTs were collected during first cycle to establish RP2D.	21 days
Primary	Part F: Number of Participants With DLT	An event was considered a DLT if it occurred within the first 21 days of treatment, and met one of following DLT criteria:hematologic toxicity- Grade4 thrombocytopenia persists for >=7 days from the time of AE onset, Grade 4 neutropenia, Grade 4 or Grade 3 febrile neutropenia persists for >=7 days, Grade4 or Grade3 anemia requiring blood transfusion, Grade 3 thrombocytopenia associated with clinically significant bleeding, Grade 3 neutropenia associated with infection as described in CTCAE version 4.0, drug related Grade 3 or 4 non-hematologic toxicity, drug related Grade 3 or 4 nonhematologic laboratory abnormality if any of the following also occur: abnormality leads to hospitalization and abnormality persists for >=7 days from the time of AE onset; drug related toxicity leading to prolonged delay (>2 weeks) in initiating Cycle 2. DLTs were collected during first cycle to establish RP2D.	21 days
Primary	Part G: Number of Participants With DLT	An event was considered a DLT if it occurred within the first 21 days of treatment, and met one of following DLT criteria:hematologic toxicity- Grade4 thrombocytopenia persists for >=7 days from the time of AE onset, Grade 4 neutropenia, Grade 4 or Grade 3 febrile neutropenia persists for >=7 days, Grade4 or Grade3 anemia requiring blood transfusion, Grade 3 thrombocytopenia associated with clinically significant bleeding, Grade 3 neutropenia associated with infection as described in CTCAE version 4.0, drug related Grade 3 or 4 non-hematologic toxicity, drug related Grade 3 or 4 nonhematologic laboratory abnormality if any of the following also occur: abnormality leads to hospitalization and abnormality persists for >=7 days from the time of AE onset; drug related toxicity leading to prolonged delay (>2 weeks) in initiating Cycle 2. DLTs were planned to be collected during first cycle to establish RP2D.	21 days
Primary	Part H: Number of Participants With DLT	An event was considered a DLT if it occurred within the first 21 days of treatment, and met one of following DLT criteria:hematologic toxicity- Grade4 thrombocytopenia persists for >=7 days from the time of AE onset, Grade 4 neutropenia, Grade 4 or Grade 3 febrile neutropenia persists for >=7 days, Grade4 or Grade3 anemia requiring blood transfusion, Grade 3 thrombocytopenia associated with clinically significant bleeding, Grade 3 neutropenia associated with infection as described in CTCAE version 4.0, drug related Grade 3 or 4 non-hematologic toxicity, drug related Grade 3 or 4 nonhematologic laboratory abnormality if any of the following also occur: abnormality leads to hospitalization and abnormality persists for >=7 days from the time of AE onset; drug related toxicity leading to prolonged delay (>2 weeks) in initiating Cycle 2. DLTs were planned to be collected during first cycle to establish RP2D.	21 days
Primary	Part I: Number of Participants With DLT	An event was considered a DLT if it occurred within the first 21 days of treatment, and met one of following DLT criteria:hematologic toxicity- Grade4 thrombocytopenia persists for >=7 days from the time of AE onset, Grade 4 neutropenia, Grade 4 or Grade 3 febrile neutropenia persists for >=7 days, Grade4 or Grade3 anemia requiring blood transfusion, Grade 3 thrombocytopenia associated with clinically significant bleeding, Grade 3 neutropenia associated with infection as described in CTCAE version 4.0, drug related Grade 3 or 4 non-hematologic toxicity, drug related Grade 3 or 4 nonhematologic laboratory abnormality if any of the following also occur: abnormality leads to hospitalization and abnormality persists for >=7 days from the time of AE onset; drug related toxicity leading to prolonged delay (>2 weeks) in initiating Cycle 2. DLTs were planned to be collected during first cycle to establish RP2D.	21 days
Primary	Part A: Number of Participants With Non-serious Treatment-emergent Adverse Events (TEAEs), Serious TEAEs (STEAEs) and Adverse Events of Special Interest (AESIs)	An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of a study treatment, whether or not considered related to the study treatment. An SAE is defined as any untoward medical occurrence that, at any dose; results in death, is life-threatening, requires inpatient hospitalization or prolongation of existing hospitalization, results in persistent or significant disability/incapacity, is a congenital anomaly/birth defect or any other situation according to medical or scientific judgement. TEAE is any event that was not present prior to the initiation of study treatment or any event already present that worsens in either intensity or frequency following exposure to study treatment. Number of participants with TEAEs, SAEs and AESIs are reported.	Up to 28.5 months
Primary	Part B: Number of Participants With Non-serious TEAEs, STEAEs and AESIs	An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of a study treatment, whether or not considered related to the study treatment. An SAE is defined as any untoward medical occurrence that, at any dose; results in death, is life-threatening, requires inpatient hospitalization or prolongation of existing hospitalization, results in persistent or significant disability/incapacity, is a congenital anomaly/birth defect or any other situation according to medical or scientific judgement. TEAE is any event that was not present prior to the initiation of study treatment or any event already present that worsens in either intensity or frequency following exposure to study treatment. Number of participants with TEAEs, SAEs and AESIs are reported.	Up to 28.5 months
Primary	Part C: Number of Participants With Non-serious TEAEs, STEAEs and AESIs	An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of a study treatment, whether or not considered related to the study treatment. An SAE is defined as any untoward medical occurrence that, at any dose; results in death, is life-threatening, requires inpatient hospitalization or prolongation of existing hospitalization, results in persistent or significant disability/incapacity, is a congenital anomaly/birth defect or any other situation according to medical or scientific judgement. TEAE is any event that was not present prior to the initiation of study treatment or any event already present that worsens in either intensity or frequency following exposure to study treatment. Number of participants with TEAEs, SAEs and AESIs are reported.	Up to 22.5 months
Primary	Part D: Number of Participants With Non-serious TEAEs, STEAEs and AESIs	An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of a study treatment, whether or not considered related to the study treatment. An SAE is defined as any untoward medical occurrence that, at any dose; results in death, is life-threatening, requires inpatient hospitalization or prolongation of existing hospitalization, results in persistent or significant disability/incapacity, is a congenital anomaly/birth defect or any other situation according to medical or scientific judgement. TEAE is any event that was not present prior to the initiation of study treatment or any event already present that worsens in either intensity or frequency following exposure to study treatment. Number of participants with TEAEs, SAEs and AESIs are reported.	Up to 9.5 months
Primary	Part E: Number of Participants With Non-serious TEAEs, STEAEs and AESIs	An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of a study treatment, whether or not considered related to the study treatment. An SAE is defined as any untoward medical occurrence that, at any dose; results in death, is life-threatening, requires inpatient hospitalization or prolongation of existing hospitalization, results in persistent or significant disability/incapacity, is a congenital anomaly/birth defect or any other situation according to medical or scientific judgement. TEAE is any event that was not present prior to the initiation of study treatment or any event already present that worsens in either intensity or frequency following exposure to study treatment. Number of participants with TEAEs, SAEs and AESIs are reported.	Up to 4.4 months
Primary	Part F: Number of Participants With Non-serious TEAEs, STEAEs and AESIs	An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of a study treatment, whether or not considered related to the study treatment. An SAE is defined as any untoward medical occurrence that, at any dose; results in death, is life-threatening, requires inpatient hospitalization or prolongation of existing hospitalization, results in persistent or significant disability/incapacity, is a congenital anomaly/birth defect or any other situation according to medical or scientific judgement. TEAE is any event that was not present prior to the initiation of study treatment or any event already present that worsens in either intensity or frequency following exposure to study treatment. Number of participants with TEAEs, SAEs and AESIs are reported.	Up to 3.5 months
Primary	Part G: Number of Participants With Non-serious TEAEs, STEAEs and AESIs	An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of a study treatment, whether or not considered related to the study treatment. An SAE is defined as any untoward medical occurrence that, at any dose; results in death, is life-threatening, requires inpatient hospitalization or prolongation of existing hospitalization, results in persistent or significant disability/incapacity, is a congenital anomaly/birth defect or any other situation according to medical or scientific judgement. TEAE is any event that was not present prior to the initiation of study treatment or any event already present that worsens in either intensity or frequency following exposure to study treatment.	Up to 24 months
Primary	Part H: Number of Participants With Non-serious TEAEs, STEAEs and AESIs	An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of a study treatment, whether or not considered related to the study treatment. An SAE is defined as any untoward medical occurrence that, at any dose; results in death, is life-threatening, requires inpatient hospitalization or prolongation of existing hospitalization, results in persistent or significant disability/incapacity, is a congenital anomaly/birth defect or any other situation according to medical or scientific judgement. TEAE is any event that was not present prior to the initiation of study treatment or any event already present that worsens in either intensity or frequency following exposure to study treatment.	Up to 24 months
Primary	Part I: Number of Participants With Non-serious TEAEs, STEAEs and AESIs	An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of a study treatment, whether or not considered related to the study treatment. An SAE is defined as any untoward medical occurrence that, at any dose; results in death, is life-threatening, requires inpatient hospitalization or prolongation of existing hospitalization, results in persistent or significant disability/incapacity, is a congenital anomaly/birth defect or any other situation according to medical or scientific judgement. TEAE is any event that was not present prior to the initiation of study treatment or any event already present that worsens in either intensity or frequency following exposure to study treatment.	Up to 24 months
Secondary	Part A: Objective Response Rate	Objective Response Rate is defined as the percentage of participants who achieved confirmed complete response (CR) or partial response (PR), evaluated using Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 based on Investigator assessment; where CR=Disappearance of all target lesions. Any pathological lymph nodes must be <10 millimeters (mm) in the short axis. PR=At least a 30 percent (%) decrease in the sum of the diameters of target lesions, taking as a reference, the Baseline sum of the diameters.	Up to 28.5 months
Secondary	Part B: Objective Response Rate	Objective Response Rate is defined as the percentage of participants who achieved confirmed CR or PR, evaluated using RECIST version 1.1 based on Investigator assessment; where CR=Disappearance of all target lesions. Any pathological lymph nodes must be <10 mm in the short axis. PR=At least a 30% decrease in the sum of the diameters of target lesions, taking as a reference, the Baseline sum of the diameters.	Up to 28.5 months
Secondary	Part C: Objective Response Rate	Objective Response Rate is defined as the percentage of participants who achieved confirmed CR or PR, evaluated using RECIST version 1.1 based on Investigator assessment; where CR=Disappearance of all target lesions. Any pathological lymph nodes must be <10 mm in the short axis. PR=At least a 30% decrease in the sum of the diameters of target lesions, taking as a reference, the Baseline sum of the diameters.	Up to 22.5 months
Secondary	Part D: Objective Response Rate	Objective Response Rate is defined as the percentage of participants who achieved confirmed CR or PR, evaluated using RECIST version 1.1 based on Investigator assessment; where CR=Disappearance of all target lesions. Any pathological lymph nodes must be <10 mm in the short axis. PR=At least a 30% decrease in the sum of the diameters of target lesions, taking as a reference, the Baseline sum of the diameters.	Up to 9.5 months
Secondary	Part E: Objective Response Rate	Objective Response Rate is defined as the percentage of participants who achieved confirmed CR or PR, evaluated using RECIST version 1.1 based on Investigator assessment; where CR=Disappearance of all target lesions. Any pathological lymph nodes must be <10 mm in the short axis. PR=At least a 30% decrease in the sum of the diameters of target lesions, taking as a reference, the Baseline sum of the diameters.	Up to 4.4 months
Secondary	Part F: Objective Response Rate	Objective Response Rate is defined as the percentage of participants who achieved confirmed CR or PR, evaluated using RECIST version 1.1 based on Investigator assessment; where CR=Disappearance of all target lesions. Any pathological lymph nodes must be <10 mm in the short axis. PR=At least a 30% decrease in the sum of the diameters of target lesions, taking as a reference, the Baseline sum of the diameters.	Up to 3.5 months
Secondary	Part G: Objective Response Rate	Objective Response Rate is defined as the percentage of participants who achieved confirmed CR or PR, evaluated using RECIST version 1.1 based on Investigator assessment; where CR=Disappearance of all target lesions. Any pathological lymph nodes must be <10 mm in the short axis. PR=At least a 30% decrease in the sum of the diameters of target lesions, taking as a reference, the Baseline sum of the diameters.	Up to 24 months
Secondary	Part H: Objective Response Rate	Objective Response Rate is defined as the percentage of participants who achieved confirmed CR or PR, evaluated using RECIST version 1.1 based on Investigator assessment; where CR=Disappearance of all target lesions. Any pathological lymph nodes must be <10 mm in the short axis. PR=At least a 30% decrease in the sum of the diameters of target lesions, taking as a reference, the Baseline sum of the diameters.	Up to 24 months
Secondary	Part I: Objective Response Rate	Objective Response Rate is defined as the percentage of participants who achieved confirmed CR or PR, evaluated using RECIST version 1.1 based on Investigator assessment; where CR=Disappearance of all target lesions. Any pathological lymph nodes must be <10 mm in the short axis. PR=At least a 30% decrease in the sum of the diameters of target lesions, taking as a reference, the Baseline sum of the diameters.	Up to 24 months
Secondary	Part A: Duration of Response	Duration of response is defined as the time from first documentation of response (CR or PR) until the time of first documentation of disease progression by RECIST version 1.1 or death by any cause.	Up to 28.5 months
Secondary	Part B: Duration of Response	Duration of response is defined as the time from first documentation of response (CR or PR) until the time of first documentation of disease progression by RECIST version 1.1 or death by any cause. Data is not reported as participants response is still ongoing at the time of primary analysis.	Up to 28.5 months
Secondary	Part C: Duration of Response	Duration of response is defined as the time from first documentation of response (CR or PR) until the time of first documentation of disease progression by RECIST version 1.1 or death by any cause. Data is not reported as participants response is still ongoing at the time of primary analysis.	Up to 22.5 months
Secondary	Part D: Duration of Response	Duration of response is defined as the time from first documentation of response (CR or PR) until the time of first documentation of disease progression by RECIST version 1.1 or death by any cause. Data is not reported as participants response is still ongoing at the time of primary analysis.	Up to 9.5 months
Secondary	Part E: Duration of Response	Duration of response is defined as the time from first documentation of response (CR or PR) until the time of first documentation of disease progression by RECIST version 1.1 or death by any cause.	Up to 4.4 months
Secondary	Part F: Duration of Response	Duration of response is defined as the time from first documentation of response (CR or PR) until the time of first documentation of disease progression by RECIST version 1.1 or death by any cause.	Up to 3.5 months
Secondary	Part G: Duration of Response	Duration of response is defined as the time from first documentation of response (CR or PR) until the time of first documentation of disease progression by RECIST version 1.1 or death by any cause.	Up to 24 months
Secondary	Part H: Duration of Response	Duration of response is defined as the time from first documentation of response (CR or PR) until the time of first documentation of disease progression by RECIST version 1.1 or death by any cause.	Up to 24 months
Secondary	Part I: Duration of Response	Duration of response is defined as the time from first documentation of response (CR or PR) until the time of first documentation of disease progression by RECIST version 1.1 or death by any cause.	Up to 24 months
Secondary	Part A: Disease Control Rate	Disease Control Rate is defined as the percentage of participants who had achieved CR, PR, or stable disease (SD) per RECIST version 1.1.	Up to 28.5 months
Secondary	Part B: Disease Control Rate	Disease Control Rate is defined as the percentage of participants who had achieved CR, PR, or SD per RECIST version 1.1.	Up to 28.5 months
Secondary	Part C: Disease Control Rate	Disease Control Rate is defined as the percentage of participants who had achieved CR, PR, or SD per RECIST version 1.1.	Up to 22.5 months
Secondary	Part D: Disease Control Rate	Disease Control Rate is defined as the percentage of participants who had achieved CR, PR, or SD per RECIST version 1.1.	Up to 9.5 months
Secondary	Part E: Disease Control Rate	Disease Control Rate is defined as the percentage of participants who had achieved CR, PR, or SD per RECIST version 1.1.	Up to 4.4 months
Secondary	Part F: Disease Control Rate	Disease Control Rate is defined as the percentage of participants who had achieved CR, PR, or SD per RECIST version 1.1.	Up to 3.5 months
Secondary	Part G: Disease Control Rate	Disease Control Rate is defined as the percentage of participants who had achieved CR, PR, or SD per RECIST version 1.1.	Up to 24 months
Secondary	Part H: Disease Control Rate	Disease Control Rate is defined as the percentage of participants who had achieved CR, PR, or SD per RECIST version 1.1.	Up to 24 months
Secondary	Part I: Disease Control Rate	Disease Control Rate is defined as the percentage of participants who had achieved CR, PR, or SD per RECIST version 1.1.	Up to 24 months
Secondary	Part A: Progression-free Survival	Progression-free Survival is defined as the date of first dose to the date of disease progression or death due to any cause, whichever occurs earlier. Progressive Disease (PD) is defined as at least a 20% increase in the sum of the diameters of target lesions, taking as reference the smallest sum on study.	Up to 28.5 months
Secondary	Part B: Progression-free Survival	Progression-free Survival is defined as the date of first dose to the date of disease progression or death due to any cause, whichever occurs earlier. PD is defined as at least a 20% increase in the sum of the diameters of target lesions, taking as reference the smallest sum on study.	Up to 28.5 months
Secondary	Part C: Progression-free Survival	Progression-free Survival is defined as the date of first dose to the date of disease progression or death due to any cause, whichever occurs earlier. PD is defined as at least a 20% increase in the sum of the diameters of target lesions, taking as reference the smallest sum on study.	Up to 22.5 months
Secondary	Part D: Progression-free Survival	Progression-free Survival is defined as the date of first dose to the date of disease progression or death due to any cause, whichever occurs earlier. PD is defined as at least a 20% increase in the sum of the diameters of target lesions, taking as reference the smallest sum on study.	Up to 9.5 months
Secondary	Part E: Progression-free Survival	Progression-free Survival is defined as the date of first dose to the date of disease progression or death due to any cause, whichever occurs earlier. PD is defined as at least a 20% increase in the sum of the diameters of target lesions, taking as reference the smallest sum on study.	Up to 4.4 months
Secondary	Part F: Progression-free Survival	Progression-free Survival is defined as the date of first dose to the date of disease progression or death due to any cause, whichever occurs earlier. PD is defined as at least a 20% increase in the sum of the diameters of target lesions, taking as reference the smallest sum on study.	Up to 3.5 months
Secondary	Part G: Progression-free Survival	Progression-free Survival is defined as the date of first dose to the date of disease progression or death due to any cause, whichever occurs earlier.	Up to 24 months
Secondary	Part H: Progression-free Survival	Progression-free Survival is defined as the date of first dose to the date of disease progression or death due to any cause, whichever occurs earlier.	Up to 24 months
Secondary	Part I: Progression-free Survival	Progression-free Survival is defined as the date of first dose to the date of disease progression or death due to any cause, whichever occurs earlier.	Up to 24 months
Secondary	Part A: Number of Participants With Positive Anti-TSR-042 Antibodies	Serum samples were collected at indicated time points and tested for the presence of antibodies that bind to TSR-042. The presence of anti-TSR-042 antibodies were assessed using a tiered approach using electrochemiluminescence (that is, screening, confirmation, titer, and neutralizing antibody assay). Anti-drug Antibody Population consisted of all participants who received at least 1 dose of study treatment and had provided a pre-dose blood sample and at least 1 post-dose blood sample at or after 96 hours.	Up to 28.5 months
Secondary	Part B: Number of Participants With Positive Anti-TSR-042 Antibodies	Serum samples were collected at indicated time points and tested for the presence of antibodies that bind to TSR-042. The presence of anti-TSR-042 antibodies were assessed using a tiered approach using electrochemiluminescence (that is, screening, confirmation, titer, and neutralizing antibody assay).	Up to 28.5 months
Secondary	Part C: Number of Participants With Positive Anti-TSR-042 Antibodies	Serum samples were collected at indicated time points and tested for the presence of antibodies that bind to TSR-042. The presence of anti-TSR-042 antibodies were assessed using a tiered approach using electrochemiluminescence (that is, screening, confirmation, titer, and neutralizing antibody assay).	Up to 22.5 months
Secondary	Part D: Number of Participants With Positive Anti-TSR-042 Antibodies	Serum samples were collected at indicated time points and tested for the presence of antibodies that bind to TSR-042. The presence of anti-TSR-042 antibodies were assessed using a tiered approach using electrochemiluminescence (that is, screening, confirmation, titer, and neutralizing antibody assay).	Up to 9.5 months
Secondary	Part E: Number of Participants With Positive Anti-TSR-042 Antibodies	Serum samples were collected at indicated time points and tested for the presence of antibodies that bind to TSR-042. The presence of anti-TSR-042 antibodies were assessed using a tiered approach using electrochemiluminescence (that is, screening, confirmation, titer, and neutralizing antibody assay).	Up to 4.4 months
Secondary	Part F: Number of Participants With Positive Anti-TSR-042 Antibodies	Serum samples were collected at indicated time points and tested for the presence of antibodies that bind to TSR-042. The presence of anti-TSR-042 antibodies were assessed using a tiered approach using electrochemiluminescence (that is, screening, confirmation, titer, and neutralizing antibody assay).	Up to 3.5 months
Secondary	Part F: Number of Participants With Positive Anti-TSR-022 Antibodies	Serum samples were collected at indicated time points and tested for the presence of antibodies that bind to TSR-022. The presence of anti-TSR-022 antibodies were assessed using a tiered approach using electrochemiluminescence (that is, screening, confirmation, titer, and neutralizing antibody assay).	Up to 3.5 months
Secondary	Part G: Number of Participants With Positive Anti-TSR-042 Antibodies	Serum samples were planned to be collected at indicated time points and tested for the presence of antibodies that bind to TSR-042. The presence of anti-TSR-042 antibodies were planeed to be assessed using a tiered approach using electrochemiluminescence (that is, screening, confirmation, titer, and neutralizing antibody assay).	Up to 24 months
Secondary	Part H: Number of Participants With Positive Anti-TSR-042 Antibodies	Serum samples were planned to be collected at indicated time points and tested for the presence of antibodies that bind to TSR-042. The presence of anti-TSR-042 antibodies were planned to be assessed using a tiered approach using electrochemiluminescence (that is, screening, confirmation, titer, and neutralizing antibody assay).	Up to 24 months
Secondary	Part H: Number of Participants With Positive Anti-TSR-022 Antibodies	Serum samples were planned to be collected at indicated time points and tested for the presence of antibodies that bind to TSR-022. The presence of anti-TSR-022 antibodies were planned to be assessed using a tiered approach using electrochemiluminescence (that is, screening, confirmation, titer, and neutralizing antibody assay).	Up to 24 months
Secondary	Part I: Number of Participants With Positive Anti-TSR-042 Antibodies	Serum samples were planned to be collected at indicated time points and tested for the presence of antibodies that bind to TSR-042. The presence of anti-TSR-042 antibodies were planned to be assessed using a tiered approach using electrochemiluminescence (that is, screening, confirmation, titer, and neutralizing antibody assay).	Up to 24 months
Secondary	Part I: Number of Participants With Positive Anti-TSR-022 Antibodies	Serum samples were planned to be collected at indicated time points and tested for the presence of antibodies that bind to TSR-022. The presence of anti-TSR-022 antibodies were planned to be assessed using a tiered approach using electrochemiluminescence (that is, screening, confirmation, titer, and neutralizing antibody assay).	Up to 24 months
Secondary	Part A: Area Under the Plasma Concentration From Time Zero to t (AUC[0-t]) of Niraparib	Blood samples were collected at indicated time points. Pharmacokinetic (PK) parameters of niraparib were calculated using non-compartmental methods. PK population consisted of all participants who received at least 1 dose of study treatment and had at least 1 PK sample.	Cycles 1 and 2: Pre-dose, 1, 2, 4, 6, 8 and 24 hours post-dose (each cycle was 21 days)
Secondary	Part A: AUC(0-t) of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycles 1 and 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part B: AUC0-t of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycles 1 and 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part C: AUC0-t of Niraparib	Blood samples were collected at indicated time points. PK parameters of niraparib were calculated using non-compartmental methods.	Cycles 1 and 2: Pre-dose, 1, 2, 4, 6, 8 and 24 hours post-dose (each cycle was 21 days)
Secondary	Part C: AUC0-t of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycles 1 and 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part D: AUC0-t of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycles 1 and 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part E: AUC0-t of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose; Cycle 2: Pre-dose (each cycle was 21 days)
Secondary	Part F: AUC0-t of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose; Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part F: AUC0-t of TSR-022	Blood samples were collected at indicated time points. PK parameters of TSR-022 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose; Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part G: AUC0-t of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycles 1 and 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose; Cycle 2: Pre-dose (each cycle was 21 days)
Secondary	Part H: AUC0-t of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose; Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part H: AUC0-t of TSR-022	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose; Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part I: AUC0-t of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose; Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part I: AUC0-t of TSR-022	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose; Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part A: Area Under the Plasma Concentration From Time Zero to Infinity (AUC[0-infinity]) of Niraparib	Blood samples were collected at indicated time points. PK parameters of niraparib were calculated using non-compartmental methods.	Cycles 1 and 2: Pre-dose, 1, 2, 4, 6, 8 and 24 hours post-dose (each cycle was 21 days)
Secondary	Part A: AUC(0-infinity) of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycles 1 and 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part B: AUC(0-infinity) of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycles 1 and 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part C: AUC(0-infinity) of Niraparib	Blood samples were collected at indicated time points. PK parameters of niraparib were calculated using non-compartmental methods.	Cycles 1 and 2: Pre-dose, 1, 2, 4, 6, 8 and 24 hours post-dose (each cycle was 21 days)
Secondary	Part C: AUC(0-infinity) of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycles 1 and 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part D: AUC(0-infinity) of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycles 1 and 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part E: AUC(0-infinity) of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose; Cycle 2: Pre-dose (each cycle was 21 days)
Secondary	Part F: AUC(0-infinity) of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168, and 336 hours post-dose; Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part F: AUC(0-infinity) of TSR-022	Blood samples were collected at indicated time points. PK parameters of TSR-022 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose; Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168 and 336 hours post-dose (each cycle was 21 days)
Secondary	Part G: AUC(0-infinity) of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycles 1 and 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose; Cycle 2: Pre-dose (each cycle was 21 days)
Secondary	Part H: AUC(0-infinity) of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose; Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part H: AUC(0-infinity) of TSR-022	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose; Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part I: AUC(0-infinity) of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose; Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part I: AUC(0-infinity) of TSR-022	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose; Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part A: Observed Concentration at the End of the Dosing Interval (Ctau) of Niraparib	Blood samples were collected at indicated time points. PK parameters of niraparib were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 1, 2, 4, 6, 8 and 24 hours post-dose (each cycle was 21 days)
Secondary	Part A: Ctau of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose (each cycle was 21 days)
Secondary	Part B: Ctau of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose (each cycle was 21 days)
Secondary	Part C: Ctau of Niraparib	Blood samples were collected at indicated time points. PK parameters of niraparib were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 1, 2, 4, 6, 8 and 24 hours post-dose (each cycle was 21 days)
Secondary	Part C: Ctau of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose (each cycle was 21 days)
Secondary	Part D: Ctau of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose (each cycle was 21 days)
Secondary	Part E: Ctau of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part F: Ctau of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part F: Ctau of TSR-022	Blood samples were collected at indicated time points. PK parameters of TSR-022 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part G: Ctau of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part H: Ctau of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose (each cycle was 21 days)
Secondary	Part H: Ctau of TSR-022	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose (each cycle was 21 days)
Secondary	Part I: Ctau of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose (each cycle was 21 days)
Secondary	Part I: Ctau of TSR-022	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose (each cycle was 21 days)
Secondary	Part A: Maximum Observed Plasma (Cmax) of Niraparib	Blood samples were collected at indicated time points. PK parameters of niraparib were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 1, 2, 4, 6, 8 and 24 hours post-dose (each cycle was 21 days)
Secondary	Part A: Cmax of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose (each cycle was 21 days)
Secondary	Part B: Cmax of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose (each cycle was 21 days)
Secondary	Part C: Cmax of Niraparib	Blood samples were collected at indicated time points. PK parameters of niraparib were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 1, 2, 4, 6, 8 and 24 hours post-dose (each cycle was 21 days)
Secondary	Part C: Cmax of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose (each cycle was 21 days)
Secondary	Part D: Cmax of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose (each cycle was 21 days)
Secondary	Part E: Cmax of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part F: Cmax of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part F: Cmax of TSR-022	Blood samples were collected at indicated time points. PK parameters of TSR-022 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose (each cycle was 21 days)
Secondary	Part G: Cmax of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part H: Cmax of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose (each cycle was 21 days)
Secondary	Part H: Cmax of TSR-022	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose (each cycle was 21 days)
Secondary	Part I: Cmax of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose (each cycle was 21 days)
Secondary	Part I: Cmax of TSR-022	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose (each cycle was 21 days)
Secondary	Part A: Clearance After Oral Administration (CL/F) of Niraparib	Blood samples were collected at indicated time points. PK parameters of niraparib were calculated using non-compartmental methods.	Cycles 1 and 2: Pre-dose, 1, 2, 4, 6, 8 and 24 hours post-dose (each cycle was 21 days)
Secondary	Part A: Clearance After Intravenous Administration (CL) of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycles 1 and 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part B: CL of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycles 1 and 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part C: CL/F of Niraparib	Blood samples were collected at indicated time points. PK parameters of niraparib were calculated using non-compartmental methods.	Cycles 1 and 2: Pre-dose, 1, 2, 4, 6, 8 and 24 hours post-dose (each cycle was 21 days)
Secondary	Part C: CL of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycles 1 and 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part D: CL of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycles 1 and 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part E: CL of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose; Cycle 2: Pre-dose (each cycle was 21 days)
Secondary	Part F: CL of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168, and 336 hours post-dose; Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part F: CL of TSR-022	Blood samples were collected at indicated time points. PK parameters of TSR-022 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168, and 336 hours post-dose; Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part G: CL of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycles 1 and 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose; Cycle 2: Pre-dose (each cycle was 21 days)
Secondary	Part H: CL of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose; Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part H: CL of TSR-022	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose; Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part I: CL of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose; Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part I: CL of TSR-022	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose; Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part A: Volume of Distribution After Oral Administration (Vz/F) of Niraparib	Blood samples were collected at indicated time points. PK parameters of niraparib were calculated using non-compartmental methods.	Cycles 1 and 2: Pre-dose, 1, 2, 4, 6, 8 and 24 hours post-dose (each cycle was 21 days)
Secondary	Part A: Volume of Distribution After Intravenous Administration (Vz) of of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycles 1 and 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part B: Vz of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycles 1 and 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part C: Vz/F of Niraparib	Blood samples were collected at indicated time points. PK parameters of niraparib were calculated using non-compartmental methods.	Cycles 1 and 2: Pre-dose, 1, 2, 4, 6, 8 and 24 hours post-dose (each cycle was 21 days)
Secondary	Part C: Vz of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycles 1 and 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part D: Vz of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycles 1 and 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part E: Vz of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose; Cycle 2: Pre-dose (each cycle was 21 days)
Secondary	Part F: Vz of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168, and 336 hours post-dose; Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part F: Vz of TSR-022	Blood samples were collected at indicated time points. PK parameters of TSR-022 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168, and 336 hours post-dose; Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part G: Vz of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycles 1 and 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose; Cycle 2: Pre-dose (each cycle was 21 days)
Secondary	Part H: Vz of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose; Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part H: Vz of TSR-022	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose; Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part I: Vz of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose; Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part I: Vz of TSR-022	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose; Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part A: AUC at Steady State (AUCss) of Niraparib	Blood samples were collected at indicated time points. PK parameters of niraparib were calculated using non-compartmental methods.	Cycle 2: Pre-dose, 1, 2, 4, 6, 8 and 24 hours post-dose (each cycle was 21 days)
Secondary	Part A: AUCss of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part B: AUCss of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part C: AUCss of Niraparib	Blood samples were collected at indicated time points. PK parameters of niraparib were calculated using non-compartmental methods.	Cycle 2: Pre-dose, 1, 2, 4, 6, 8 and 24 hours post-dose (each cycle was 21 days)
Secondary	Part C: AUCss of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part D: AUCss of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part E: AUCss of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 2: Pre-dose (each cycle was 21 days)
Secondary	Part F: AUCss of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part F: AUCss of TSR-022	Blood samples were collected at indicated time points. PK parameters of TSR-022 were calculated using non-compartmental methods.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part G: AUCss of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part H: AUCss of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part H: AUCss of TSR-022	Blood samples were planned to be collected at indicated time points.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part I: AUCss of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part I: AUCss of TSR-022	Blood samples were planned to be collected at indicated time points.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part A: Ctau at Steady State (Ctau,ss) of Niraparib	Blood samples were collected at indicated time points. PK parameters of niraparib were calculated using non-compartmental methods.	Cycle 2: Pre-dose, 1, 2, 4, 6, 8 and 24 hours post-dose; Cycles 5 and 11: Pre-dose, 2 hours post-dose (each cycle was 21 days)
Secondary	Part A: Ctau,ss of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part B: Ctau,ss of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part C: Ctau,ss of Niraparib	Blood samples were collected at indicated time points. PK parameters of niraparib were calculated using non-compartmental methods.	Cycle 2: Pre-dose, 1, 2, 4, 6, 8 and 24 hours post-dose; Cycles 5 and 11: Pre-dose, 2 hours post-dose (each cycle was 21 days)
Secondary	Part C: Ctau,ss of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part D: Ctau,ss of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part E: Ctau,ss of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 2: Pre-dose (each cycle was 21 days)
Secondary	Part F: Ctau,ss of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part F: Ctau,ss of TSR-022	Blood samples were collected at indicated time points. PK parameters of TSR-022 were calculated using non-compartmental methods.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part G: Ctau,ss of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part H: Ctau,ss of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part H: Ctau,ss of TSR-022	Blood samples were planned to be collected at indicated time points.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part I: Ctau,ss of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part I: Ctau,ss of TSR-022	Blood samples were planned to be collected at indicated time points.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part A: Cmax at Steady State (Cmax,ss) of Niraparib	Blood samples were collected at indicated time points. PK parameters of niraparib were calculated using non-compartmental methods.	Cycle 2: Pre-dose, 1, 2, 4, 6, 8 and 24 hours post-dose; Cycles 5 and 11: Pre-dose, 2 hours post-dose (each cycle was 21 days)
Secondary	Part A: Cmax,ss of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part B: Cmax,ss of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part C: Cmax,ss of Niraparib	Blood samples were collected at indicated time points. PK parameters of niraparib were calculated using non-compartmental methods.	Cycle 2: Pre-dose, 1, 2, 4, 6, 8 and 24 hours post-dose; Cycles 5 and 11: Pre-dose, 2 hours post-dose (each cycle was 21 days)
Secondary	Part C: Cmax,ss of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part D: Cmax,ss of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part E: Cmax,ss of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 2: Pre-dose (each cycle was 21 days)
Secondary	Part F: Cmax,ss of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part F: Cmax,ss of TSR-022	Blood samples were collected at indicated time points. PK parameters of TSR-022 were calculated using non-compartmental methods.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part G: Cmax,ss of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part H: Cmax,ss of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part H: Cmax,ss of TSR-022	Blood samples were planned to be collected at indicated time points.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part I: Cmax,ss of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part I: Cmax,ss of TSR-022	Blood samples were planned to be collected at indicated time points.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part A: Time to Reach Maximum Plasma Concentration (Tmax) of Niraparib	Blood samples were collected at indicated time points. PK parameters of niraparib were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 1, 2, 4, 6, 8 and 24 hours post-dose (each cycle was 21 days)
Secondary	Part A: Tmax of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose (each cycle was 21 days)
Secondary	Part B: Tmax of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose (each cycle was 21 days)
Secondary	Part C: Tmax of Niraparib	Blood samples were collected at indicated time points. PK parameters of niraparib were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 1, 2, 4, 6, 8 and 24 hours post-dose (each cycle was 21 days)
Secondary	Part C: Tmax of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose (each cycle was 21 days)
Secondary	Part D: Tmax of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose (each cycle was 21 days)
Secondary	Part E: Tmax of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part F: Tmax of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part F: Tmax of TSR-022	Blood samples were collected at indicated time points. PK parameters of TSR-022 were calculated using non-compartmental methods.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part G: Tmax of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part H: Tmax of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose (each cycle was 21 days)
Secondary	Part H: Tmax of TSR-022	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose (each cycle was 21 days)
Secondary	Part I: Tmax of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose (each cycle was 21 days)
Secondary	Part I: Tmax of TSR-022	Blood samples were planned to be collected at indicated time points.	Cycle 1: Pre-dose, 0.5, 1, 2, 3, 24, 48, 96, 168 and 336 hours post-dose (each cycle was 21 days)
Secondary	Part A: Tmax at Steady State (Tmax,ss) of Niraparib	Blood samples were collected at indicated time points. PK parameters of niraparib were calculated using non-compartmental methods.	Cycle 2: Pre-dose, 1, 2, 4, 6, 8 and 24 hours post-dose; Cycles 5 and 11: Pre-dose, 2 hours post-dose (each cycle was 21 days)
Secondary	Part A: Tmax,ss of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part B: Tmax,ss of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part C: Tmax,ss of Niraparib	Blood samples were collected at indicated time points. PK parameters of niraparib were calculated using non-compartmental methods.	Cycle 2: Pre-dose, 1, 2, 4, 6, 8 and 24 hours post-dose; Cycles 5 and 11: Pre-dose, 2 hours post-dose (each cycle was 21 days)
Secondary	Part C: Tmax,ss of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part D: Tmax,ss of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part E: Tmax,ss of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 2: Pre-dose (each cycle was 21 days)
Secondary	Part F: Tmax,ss of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part F: Tmax,ss of TSR-022	Blood samples were collected at indicated time points. PK parameters of TSR-022 were calculated using non-compartmental methods.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part G: Tmax,ss of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part H: Tmax,ss of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part H: Tmax,ss of TSR-022	Blood samples were planned to be collected at indicated time points.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part I: Tmax,ss of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part I: Tmax,ss of TSR-022	Blood samples were planned to be collected at indicated time points.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part A: Volume of Distribution After Intravenous Administration (Vss) of of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part B: Vss of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part C: Vss of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part D: Vss of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 4: Pre-dose, 0.5, 2, 24, 96, 168, 336 and 504 hours post-dose; Cycles 5 and 11: Pre-dose, 0.5, 2, 24, 96, 168, 336, 504 and 1008 hours post-dose (each cycle was 21 days)
Secondary	Part E: Vss of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 2: Pre-dose (each cycle was 21 days)
Secondary	Part F: Vss of TSR-042	Blood samples were collected at indicated time points. PK parameters of TSR-042 were calculated using non-compartmental methods.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part F: Vss of TSR-022	Blood samples were collected at indicated time points. PK parameters of TSR-022 were calculated using non-compartmental methods.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part G: Vss of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part H: Vss of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part H: Vss of TSR-022	Blood samples were planned to be collected at indicated time points.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part I: Vss of TSR-042	Blood samples were planned to be collected at indicated time points.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)
Secondary	Part I: Vss of TSR-022	Blood samples were planned to be collected at indicated time points.	Cycle 2: Pre-dose; Cycle 5: Pre-dose, 0.5, 2, 24, 48, 96, 168, and 336 hours post-dose (each cycle was 21 days)

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Study of Niraparib, TSR-022, Bevacizumab, and Platinum-Based Doublet Chemotherapy in Combination With TSR-042

Clinical Trial Details — Status: Active, not recruiting

Administrative data

Study information

Clinical Trial Summary

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Intervention

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Country where clinical trial is conducted

References & Publications (1)

Outcome