A Study Assessing Pamiparib With Radiation and/or Temozolomide (TMZ) in Participants With Newly Diagnosed or Recurrent Glioblastoma

Brain and Central Nervous System Tumors Clinical Trial

Official title:

A Phase 1b/2 Study to Assess the Safety, Tolerability and Efficacy of BGB-290 in Combination With Radiation Therapy (RT) and/or Temozolomide (TMZ) in Subjects With First-line or Recurrent/Refractory Glioblastoma

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03150862
• Other study ID #: BGB-290-104
• Secondary ID: 2017-001554-33
• Status: Completed
• Phase: Phase 1/Phase 2
• Start date: July 24, 2017
• Est. completion date: March 17, 2021

Study information

• Verified date: May 2022
• Source: BeiGene
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The primary objective of this study is to evaluate the safety, efficacy and clinical activity of Pamiparib in combination with radiation therapy (RT) and/or temozolomide (TMZ) in participants with newly diagnosed or recurrent/refractory glioblastoma.

Description:

An open-label, multiple-dose, dose-escalation study to determine the safety, pharmacokinetics (PK) and pharmacodynamics (PD) of Pamiparib in combination with radiation therapy (RT) and/or TMZ.

In dose escalation/Phase 1b, Pamiparib will be combined with RT (Arm A) or RT and TMZ (Arm B) in participants with newly diagnosed unmethylated glioblastoma (GBM) and in Arm C of the study Pamiparib will be combined with TMZ in participants with methylated or unmethylated recurrent/refractory GBM.

The dose expansion/Phase 2 phase will enroll up to 4 cohorts: participants with newly diagnosed unmethylated GBM in Arms A and B, and 2 cohorts of participants with recurrent/refractory GBM grouped by O-6-methylguanine-DNA methyltransferase (MGMT) status - unmethylated or methylated - in Arm C.

Participants in Arms A and B are treated until completion of RT and participants in Arm C may continue treatment in the absence of safety concerns and disease progression.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 116
• Est. completion date: March 17, 2021
• Est. primary completion date: March 17, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Key Inclusion Criteria: All participants

1. Age = 18 years old.

2. Confirmed diagnosis of glioblastoma (WHO Grade IV).

3. Agreement to provide archival tumor tissue for exploratory biomarker analysis

4. Ability to undergo serial MRIs.

5. Eastern Cooperative Oncology Group (ECOG) status = 1.

6. Adequate hematologic and end-organ function

7. Females of childbearing potential and non-sterile males must agree to use highly effective methods of birth control throughout the course of study and at least up to 6 months after last dosing.

8. Ability to swallow whole capsules.

Participants in Arms A and B (not Arm C) must meet inclusion criteria # 9 - 11:

9. No previous treatment for GBM except surgery.

10. Able to start radiation therapy = 49 days after surgery but = 14 days after a biopsy or =28 days after an open biopsy or craniotomy with adequate wound healing.

11. Documented unmethylated MGMT promoter status.

Participants in Arm C Escalation (Phase 1b) must meet inclusion criteria # 12 - 15:

12. Documentation of MGMT promoter status

13. No prior systemic chemotherapy other than TMZ for GBM.

14. Histologically confirmed secondary glioblastoma

15. Disease that is evaluable or measurable as defined by Response Assessment in Neuro-Oncology (RANO) criteria

Participants in Arm C Expansion (Phase 2), must meet criteria # 16 - 18:

16. Histologically confirmed de novo (primary) glioblastoma with unequivocal first progressive disease (PD) after RT with concurrent/adjuvant TMZ chemotherapy

17. Disease that is measurable as defined by RANO criteria

18. Documentation of MGMT promoter status

Key Exclusion Criteria: All participants

1. Prior chemotherapy, biologic therapy, immunotherapy or investigational agents =21 days prior to start of study treatment.

2. Toxicity of = Grade 2 from prior therapy.

3. Major surgery or significant other injury = 4 weeks prior to start of study treatment.

4. History of other active malignancies within 2 years with exception of (i) adequately treated in situ cancer of the cervix, (ii) non-melanoma skin cancer, or (iii) localized adequately treated cancer with curative intent or malignancy diagnosed > 2 years ago with no evidence of disease and no treatment = 2 years prior to study treatment.

5. Active infection requiring systemic treatment.

6. Known human immunodeficiency virus (HIV) or active viral hepatitis.

7. Active, clinically significant cardiac disease or any Class 3 or 4 cardiac disease, ventricular arrhythmia or Cerebrovascular Accident (CVA) = 6 months prior to start of treatment.

8. Active clinically significant gastrointestinal disease.

9. Active bleeding disorder = 6 months prior to start of treatment.

10. Need for therapeutic anti-coagulation with heparin, warfarin or other anticoagulants.

11. Use of any medications or food known to be strong or moderate cytochrome P450, family 3, subfamily A (CYP3A) inhibitors or strong inducers.

12. Pregnant or nursing females.

13. Significant intercurrent illness that may result in participant's death prior to death from glioblastoma.

Arms B and C Only:

14. Known hypersensitivity to any component of TMZ or decarbazine (DTIC).

15. Have hereditary problems of galactose intolerance

NOTE: Other protocol defined Inclusion/Exclusion criteria may apply.

Related Conditions & MeSH terms

• Brain and Central Nervous System Tumors
• Central Nervous System Neoplasms
• Glioblastoma
• Nervous System Neoplasms

Intervention

Drug:
• Pamiparib
Administered as specified in the treatment arm
• TMZ
Administered as specified in the treatment arm

Radiation:
• Radiation
Up to 60 Gy (total) over 6 - 7 weeks

Locations

Country	Name	City	State
Netherlands	Erasmus University Medical Center	Rotterdam
Switzerland	Universitätsspital Zuerich - Klinik fur Neurologie	Zurich
United States	Dana Farber Cancer Institute	Boston	Massachusetts
United States	Massachusetts General Hospital Pappas Center for Neuro-Oncology	Boston	Massachusetts
United States	University of Virginia Health Systems	Charlottesville	Virginia
United States	Cleveland Clinic	Cleveland	Ohio
United States	The Ohio State University	Columbus	Ohio
United States	Sarah Cannon Research Institute at Health One	Denver	Colorado
United States	Henry Ford Health Systems	Detroit	Michigan
United States	Penn State Milton S Hershey Medical Center	Hershey	Pennsylvania
United States	Health Midwest Ventures Group, LLC	Kansas City	Missouri
United States	UCLA Neuro-Oncology	Los Angeles	California
United States	SCRI / Tennessee Oncology	Nashville	Tennessee
United States	Memorial Sloan Kettering Cancer Center	New York	New York
United States	University of Oklahoma Health Sciences Center (Stephenson Cancer Center)	Oklahoma City	Oklahoma
United States	Thomas Jefferson University	Philadelphia	Pennsylvania
United States	Washington University	Saint Louis	Missouri
United States	Huntsman Cancer Center	Salt Lake City	Utah
United States	University of California at San Francisco	San Francisco	California
United States	Center for Neurosciences	Tucson	Arizona

Sponsors (1)

Lead Sponsor	Collaborator
BeiGene USA, Inc.

Countries where clinical trial is conducted

United States,  Netherlands,  Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Phase 1b Escalation Phase: Number of Participants With Dose-Limiting Toxicities (DLTs) as Assessed by CTCAE	A DLT is defined as one of the following toxicities occurring during the DLT assessment window: Grade =3 non-hematologic, non-hepatic major organ adverse event (AE) Grade 4 neutropenia lasting >7 days Grade =3 febrile neutropenia Grade 3 thrombocytopenia with clinically significant bleeding Grade 4 thrombocytopenia lasting > 3 days and requiring transfusion, or any decreased platelet count <15,000/mm3/ <15.0 x 109/L Grade =4 anemia Grade =3 total bilirubin or hepatic transaminases (ALT or AST)	Arm A:Day 1 Pamiparib dose until 4 weeks after the last RT; Arm B: Day 1 of Pamiparib and Temozolomide until 4 weeks after the last RT; Arm C: 1st cycle of 28 days
Primary	Phase 1b Escalation Phase: Number of Participants With Treatment Emergent Adverse Events (TEAEs) and Serious Adverse Events (SAEs) as Assessed by CTCAE	A treatment-emergent adverse event (TEAE) is defined as an AE that had an onset date on or after first dose of study treatment or was worsening in severity from baseline (pretreatment) up to 30 days following permanent study treatment discontinuation or initiation of new anti-cancer therapy, whichever occurs first.; An SAE is any untoward medical occurrence that, at any dose meets at least one of the following criteria: results in death, is life-threatening, requires hospitalization or prolongation of existing hospitalization, results in disability/incapacity, is a congenital anomaly/birth defect, is considered a significant medical AE based on medical judgment.	From initiation of study treatment (for TEAE) or from the date informed consent has been signed (for SAE), until 30 days after last study treatment or initiation of new anticancer therapy, whichever occurs first (up to 3 years and 7.5 months)
Primary	Phase 1b Escalation Phase Arm C: Number of Participants With Clinically Relevant Changes in Vital Signs and Clinical Laboratory Measurements		From the date of first dose up to end of study (EOS) visit (up to 3 years and 7.5 months)
Primary	Phase 2 Arm A: Modified Disease Control Rate (DCR) as Assessed by Response Assessment in Neuro-Oncology (RANO) Criteria	Modified DCR is defined as the percentage of participants with complete response (CR), partial response (PR) or stable disease (SD) per RANO criteria as the response assessment at the end-of-treatment (EOT) visit.	From the date of first dose up to first documentation of disease progression while participant is alive ( up to 3 years and 7.5 months)
Primary	Phase 2 Arm C: Objective Response Rate (ORR) as Assessed Using RANO Criteria	ORR (objective response rate) is defined as percentage of participants with best overall response of CR or PR per RANO criteria (confirmed by a subsequent tumor assessment at least four weeks apart).	From the date of first dose up to first documentation of disease progression while participant is alive (up to 3 years and 7.5 months)
Primary	Phase 1b Arm C: Number of Cycles of Treatment Received by Participants	Data shows the number of participants who received treatment for the given number of cycles.	From the date of first dose up to EOS visit ( up to 3 years and 7.5 months)
Primary	Phase 1b Arm C: Average Dose Intensity of Pamiparib And TMZ Received Per Participant	The average dose intensity per participant = total dose (mg) per participant / duration of treatment (days).	From the date of first dose until EOS visit (up to 3 years and 7.5 months)
Secondary	Phase 1B and Phase 2: Pharmacokinetics: Ctrough of Pamiparib		Pre-dose, 2 hours post dose on Days 1 and 15 of radiation Therapy
Secondary	Phase 1b Arm A and Arm B Escalation Phase: Modified Disease Control Rate as Assessed by RANO Criteria	Modified DCR is defined as the percentage of participants with complete response (CR), partial response (PR) or stable disease (SD) per RANO criteria as the response assessment at the end-of-treatment (EOT) visit.	From the date of first dose up to first documentation of disease progression while participant is alive (approximately 3 years and 7.5 months)
Secondary	Phase 1b Escalation Phase Arm C: Disease Control Rate as Assessed by RANO Criteria	DCR is defined as the percentage of participants with best overall response of CR, PR or SD per RANO criteria. CR or PR will be confirmed by a subsequent tumor assessment at least four weeks apart	From the date of first dose up to first documentation of disease progression while participant is alive (up to 3 years and 7.5 months)
Secondary	Phase 1b and Phase 2 Arms A and B: ORR as Assessed Using RANO Criteria	ORR is defined as percentage of participants with best overall response of CR or PR per RANO criteria (confirmed by a subsequent tumor assessment at least four weeks apart).	From the date of first dose up to first documentation of disease progression while participant is alive ( up to 3 years and 7.5 months)
Secondary	Phase 1b and Phase 2 Arms A, B and C: Clinical Benefit Rate as Assessed Using RANO Criteria	Clinical benefit rate (CBR) is defined as the percentage of participants with best overall response of CR, PR or SD = 24 weeks per RANO criteria (confirmed by a subsequent tumor assessment at least four weeks apart).	From the date of first dose up to first documentation of disease progression while participant is alive (up to 3 years and 7.5 months)
Secondary	Phase 1b and Phase 2 Arms A, B and C: Duration of Response (DOR) as Assessed Using RANO Criteria	DOR is defined as the time from the date of the earliest documented response to disease progression or death for any cause whichever occurs earlier (confirmed by a subsequent tumor assessment at least four weeks apart).	From first documentation of CR or PR to first documentation of disease progression or death (up to 3 years and 7.5 months)
Secondary	Phase 1b and Phase 2 Arms A, B and C: Progression Free Survival (PFS) as Assessed Using RANO Criteria	PFS is defined as the time from the first dose date to disease progression per RANO criteria or death, whichever occurs first.	From the date of first dose up to first documentation of disease progression or death (up to 3 years and 7.5 months)
Secondary	Phase 1b and Phase 2 Arms A, B and C: Overall Survival (OS)	OS is defined as the time from the first dose date to date of death for any cause.	From the date of first dose up to the date of death (up to 3 years and 7.5 months)
Secondary	Phase 2 Arms A and C Expansion Phase: Number of Participants With Treatment Emergent Adverse Events (TEAEs) and Serious Adverse Events (SAEs)	A treatment-emergent adverse event (TEAE) is defined as an AE that had an onset date on or after first dose of study treatment or was worsening in severity from baseline (pretreatment) up to 30 days following permanent study treatment discontinuation or initiation of new anti-cancer therapy, whichever occurs first. An SAE is any untoward medical occurrence that, at any dose meets at least one of the following criteria: results in death, is life-threatening, requires hospitalization or prolongation of existing hospitalization, results in disability/incapacity, is a congenital anomaly/birth defect, is considered a significant medical AE based on medical judgment.	From initiation of study treatment (for TEAE) or from the date informed consent has been signed (for SAE), until 30 days after last study treatment or initiation of new anticancer therapy, whichever occurs first (up to 3 years and 7.5 months)
Secondary	Phase 2 Expansion Phase Arm A and C: Number of Participants With Clinically Relevant Changes in Vital Signs and Clinical Laboratory Measurements		From the date of first dose up to EOS visit (up to 3 years and 7.5 months)
Secondary	Phase 2 Arms A and C Expansion Phase: Number of Cycles of Treatment Received by Participants	Data shows the number of participants who received treatment for the given number of cycles.	From date of first dose up to EOS Visit (up to 3 years and 7.5 months)
Secondary	Phase 2 Arms A and C Expansion Phase: Average Dose Intensity of Pamiparib and TMZ Received Per Participant	The average dose intensity per participant = total dose (mg) per participant / duration of treatment (days).	From date of first dose up to EOS Visit (up to 3 years and 7.5 months)