A Study of Alisertib in Patients With Extensive Stage Small Cell Lung Cancer
Part of paid clinical trials in Daphne, Alabama.
- Sponsor
- Puma Biotechnology, Inc.
- Study ID
- NCT06095505
- Phase
- PHASE2
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Alisertib — DRUGAlisertib enteric-coated tablets
Study Details
PUMA-ALI-4201 is a Phase 2 study evaluating alisertib monotherapy in patients with pathologically-confirmed small cell lung cancer (SCLC) following progression on or after treatment with one platinum-based chemotherapy and anti-PD-L1/PD-1 immunotherapy agent. Up to one additional systemic anti-cancer therapy for SCLC is allowed, for a total of up to two prior treatment regimens. This study is intended to identify the biomarker-defined subgroup(s) that may benefit most from alisertib treatment and to evaluate the efficacy, safety, and pharmacokinetics of alisertib.
Key Dates
- Start date
- Feb 8, 2024
- Status verified
- Jun 2026
- Primary completion
- Oct 30, 2027
- Completion
- Apr 30, 2028
Study Design
- Enrollment
- 120 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Alisertib50 mg (Prior to Amendment 2) or 60 mg (Amendment 2) or 70 mg (Amendment 3 or later) of alisertib PO BID on days 1-7 of each 21-day cycle
Primary Outcome Measure
Objective response rate (ORR) within biomarker-defined subgroup [ Time Frame: From date of first dose to first confirmed Complete or Partial Response, whichever came earlier, assessed up to 36 months ]
Central Contacts
- Puma Biotechnology, Inc. Clinical Operations Senior Director(424) 248-6500
Locations (30)
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