Phase 1b Lymphoma Study of AMG 655 in Combination With Bortezomib or Vorinostat
Phase 1
Completed
- Conditions
- Low Grade LymphomaHodgkin's LymphomaLymphomaMantle Cell LymphomaNon-Hodgkin's LymphomaDiffuse Large Cell Lymphoma
- Interventions
- Registration Number
- NCT00791011
- Lead Sponsor
- Amgen
- Brief Summary
This is a multi-center, phase 1b study of AMG 655 in combination with bortezomib or vorinostat in subjects with relapsed or refractory low grade lymphoma, mantle cell lymphoma, diffuse large cell lymphoma, and Hodgkin's disease.
Part 1 is an open-label, dose-escalation phase (3+3 design) to determine the safety, tolerability and maximum tolerated dose of AMG 655 in combination with bortezomib or vorinostat. Subjects will be enrolled into one of two arms based on investigator selection (either the bortezomib + AMG 655 arm or vorinostat + AMG 655 arm).
Part 2 of the study is a dose expansion phase that will commence after dose selection of AMG 655 in combination with bortezomib in Part 1. In Part 2, subjects (n = 20) with mantle cell lymphoma will be given AMG 655 in combination with bortezomib. The dose of AMG 655 used in combination with bortezomib will be based on safety and pharmacokinetic information obtained from Part 1 as well as from ongoing AMG 655 trials.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 33
Inclusion Criteria
- Part 1: Subjects must have a pathologically confirmed diagnosis of lymphoma that is relapsed or refractory to standard treatment or for which no curative therapy is available. Lymphoma subtypes that are eligible for enrollment include low grade lymphoma, mantle cell lymphoma, diffuse large cell lymphoma, and Hodgkin's disease.
- Part 2: Subjects must have relapsed or refractory mantle cell lymphoma with at least one objective measurable disease site (ie, measurable in at least 2 perpendicular parameters). Subjects must have had at least one prior antineoplastic therapy, up to a maximum of 3. At least one therapy must have included an anthracycline. Subjects must have had documented relapse or progression following the last therapy (ie, most recent therapy given prior to enrollment). An abnormal PET scan will not constitute evaluable disease, unless verified by CT or MRI scan).
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
- Adequate hematologic, renal, hepatic and coagulation function
Exclusion Criteria
- A history of other malignancies, except: adequately treated non-melanoma skin cancer, curatively treated in-situ cancer of the cervix, or other solid tumors curatively treated with no evidence of disease for ≥ 5 years.
- A history of allogeneic stem-cell transplantation
- Primary central nervous system (CNS) tumors including primary CNS lymphoma
- Central nervous system involvement by lymphoma
- Myocardial infarction within 6 months before enrollment, symptomatic congestive heart failure (New York Heart Association >class II), unstable angina, or unstable cardiac arrhythmia requiring medication
- Vorinostat cohorts only: History of significant GI surgery or disease, which would impair intestinal absorption
- Vorinostat cohorts only: Active peptic ulcer disease
- Prior exposure to AMG 655 or other investigational TRAIL receptor agonists is not permitted
- Prior treatment with bortezomib or vorinostat is not permitted for subjects enrolling in the bortezomib and vorinostat cohorts, respectively
- Major surgery within 28 days before the first dose of AMG 655
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Cohort 2 Vorinostat AMG 655 (low dose) with vorinostat Cohort 1 Bortezomib AMG 655 (low dose) with Bortezomib Cohort 7 Bortezomib Part 2 - Mantle Cell Lymphoma subjects only: AMG 655 at dose TBD with Bortezomib Cohort 4 Vorinostat AMG 655 (intermediate dose) with Vorinostat Cohort 7 AMG 655 Part 2 - Mantle Cell Lymphoma subjects only: AMG 655 at dose TBD with Bortezomib Cohort 5 Bortezomib AMG 655 (high dose) with Bortezomib Cohort 6 Vorinostat AMG 655 (high dose) with Vorinostat Cohort 3 AMG 655 AMG 655 (intermediate dose) with Bortezomib Cohort 3 Bortezomib AMG 655 (intermediate dose) with Bortezomib Cohort 6 AMG 655 AMG 655 (high dose) with Vorinostat Cohort 5 AMG 655 AMG 655 (high dose) with Bortezomib Cohort 4 AMG 655 AMG 655 (intermediate dose) with Vorinostat Cohort 1 AMG 655 AMG 655 (low dose) with Bortezomib Cohort 2 AMG 655 AMG 655 (low dose) with vorinostat
- Primary Outcome Measures
Name Time Method Part 1: Safety: Subject incidence of treatment emergent adverse events, Dose Limiting Toxicities, the severity of adverse events and clinically significant changes in safety laboratory tests, physical examinations, or vital signs. Length of Study Part 2: Objective response rate of AMG 655 Therapy as determined by using IWG criteria at the dose selected in Part 1, in combination with Bortezomib in subjects with mantle cell lymphoma Length of Study
- Secondary Outcome Measures
Name Time Method Part 2: PK parameters for AMG 655 on a 3 week dosing schedule. Treatment and follow up phase of study. Part 2: Duration of response. Length of treatment phase. Part 1: PK parameters for AMG 655 on a 3 week dosing schedule. Treatment and follow up phase of study. Part 2: Overall survival (OS). Length of study. Part 2: Progression-Free Survival (PFS). Length of treatment phase. Part 2: Subject incidence of anti-AMG 655 antibody formation. Treatment and follow up phase of study. Part 1: Subject incidence of anti-AMG 655 antibody formation. Treatment and follow up phase of study. Part 1: Maximum tolerated dose of AMG 655 administered with bortezomib or vorinostat, if reached. First 21 days of treatment for each cohort. Part 1: Best tumor response, objective response rate and duration of response. Length of treatment phase.