Malignant Thymoma Clinical Trial
Official title:
Phase II Study Of Oral PHA-848125AC In Patients With Malignant Thymoma Previously Treated With Multiple Lines Of Chemotherapy
| Verified date | January 2019 |
| Source | Tiziana Life Sciences, PLC |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The intent of the study is to assess the antitumor activity of PHA-848125AC in patients with recurrent or metastatic, unresectable malignant thymoma previously treated with multiple lines of chemotherapy.
| Status | Terminated |
| Enrollment | 30 |
| Est. completion date | December 17, 2018 |
| Est. primary completion date | May 31, 2017 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - Signed and dated IRB/Approved Informed Consent - Histologically or cytologically proven diagnosis of unresectable B3 thymoma or thymic carcinoma recurrent or progressing after more than one prior systemic therapy for advanced / metastatic disease - Presence of measurable disease - Age >=18 years old - ECOG performance status 0-1 - Negative pregnancy test (if female in reproductive years) - Use of effective contraceptive methods if men and women of child producing potential - Adequate liver function Total Serum Bilirubin <=1.5 x upper limit of normal (ULN) Transaminases (AST/ALT) <=2.5ULN (if liver metastases are present, then <=5ULN is allowed) ALP <=2.5ULN (if liver and/or bone metastases are present, then <=5ULN is allowed) - Adequate renal function Serum Creatinine <=ULN or Creatinine Clearance calculated by Cockcroft and Gault's formula > 60 mL/min - Adequate hematologic status ANC >=1,500cells/mm3 Platelet Count >= 100,000cells/mm3 Hemoglobin >=9.0g/dL - Two weeks must have elapsed since completion of prior chemotherapy, minor surgery, radiotherapy (provided that no more than 25% of bone marrow reserve has been irradiated) - Resolution of all acute toxic effects of any prior treatments to NCI CTC (Version 3.0) grade <=1 Exclusion Criteria: - Any of the following in the past 6 months: myocardial infarction, uncontrolled cardiac arrhythmia, unstable angina, coronary/peripheral artery bypass graft, symptomatic congestive heart failure, cerebrovascular accident or transient ischemic attack, pulmonary embolism, deep vein thrombosis - Grade >1 retinopathy - Known brain metastases - Known active infections - Pregnant or breast feeding women - Diabetes mellitus uncontrolled - Gastrointestinal disease that would impact on drug absorption - Patients under treatment with anticoagulants or with coagulation disorders or with signs of hemorrhage at baseline - Patients with previous history or current presence of neurological disorders (with the exception of myasthenia gravis), including epilepsy (although controlled by anticonvulsant therapy), Parkinson's disease and extra-pyramidal syndromes. - Other severe acute or chronic medical or psychiatric condition or laboratory abnormality that make the patient inappropriate for entry into this study |
| Country | Name | City | State |
|---|---|---|---|
| Italy | Fondazione IRCCS Istituto Nazionale dei Tumori di Milano | Milano | (mi) |
| United States | NIH, Center for Cancer Research, Medical Oncology | Bethesda | Maryland |
| United States | MedStar Georgetown University Hospital | Washington | District of Columbia |
| Lead Sponsor | Collaborator |
|---|---|
| Tiziana Life Sciences, PLC |
United States, Italy,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Progression-free Survival Rate at 3 Months | The proportion of successes (i.e. patients alive and progression-free at 3 months since treatment start) out of the total number of evaluable patients. | 3 months since treatment start | |
| Secondary | Adverse Events (NCI CTCAE) and Hematological and Blood Chemistry Parameters | The adverse events (AEs) were coded with the Medical Dictionary for Regulatory Activities (MedDRA) and their severity graded according to the NCI Common Terminology Criteria for Adverse Events (CTCAE) version 3.0. The following subsets of AEs were considered: serious AEs, AEs with CTCAE grade 3-5, AEs with a relationship to study treatment classified by the Investigator as possible or probable or definite and AEs reported as leading to discontinuation from treatment. Laboratory test values were graded according to the NCI CTCAE scale, v3.0, whenever possible. For each laboratory test included in the NCI CTCAE system, the incidence of abnormalities were evaluated by considering the worst occurrence for each patient throughout the whole treatment period. |
Adverse events: from date treatment consent signed to 28 days after last treatment; hematology/blood chemistry tests: at baseline and between Day 11-14 of each cycle of a maximum total of 48 two-week cycles. | |
| Secondary | Objective Response Rate (ORR) | Point and 95% confidence interval estimates was calculated for the objective tumor response rate (confirmed CRs or PRs). The determination of antitumor efficacy was based on objective tumor assessments made according to the RECIST guideline (version 1.1). The analysis was performed in the evaluable population. | Assessments were made every 6 weeks from start date until PD or up to a maximum duration of 134 weeks. | |
| Secondary | Disease Control Rate (ORR+SD Rate) | Point and 95% confidence interval estimates was calculated for the disease control rate (confirmed CRs / PRs and SD > or = 6 weeks). The analysis was performed in the evaluable patient populations. | Assessments were made every 6 weeks from start date until PD or up to a maximum duration of 134 weeks. | |
| Secondary | Duration of Response | Calculated in patients achieving a confirmed objective tumor response by RECIST version 1.1 criteria. | Assessments were made every 6 weeks from start date until PD or up to a maximum duration of 134 weeks. | |
| Secondary | Overall Survival | The length of time from either the date of diagnosis or the start of treatment for a disease, such as cancer, and to the date in which the patients diagnosed with the disease are still alive. Kaplan-Meier estimates as percentage of patients alive. | Every 6 weeks during Follow-Up until PD or new therapy start; every 6 months thereafter, up to 2 years from the last dose of study drug. | |
| Secondary | Progression-free Survival (PFS) | The length of time during and after the treatment of a disease, such as cancer, that a patient lives with the disease but it does not get worse. In a clinical trial, measuring the progression-free survival is one way to see how well a new treatment works. | Assessments were made every 6 weeks from start date until PD or up to a maximum duration of 134 weeks. |