Selective HDAC6 Inhibitor ACY 241 in Combination With Nivolumab in Patients With Unresectable Non Small Cell Lung Cancer
Part of paid clinical trials in Boston, Massachusetts.
- Sponsor
- Celgene
- Study ID
- NCT02635061
- Phase
- PHASE1
- Status
- Terminated
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- ACY-241 — DRUGSpecified dose on specified days
- Nivolumab — DRUGSpecified dose on specified days
Study Details
Determine the safety, tolerability, dose limiting toxicities (DLTs), and maximum tolerated dose (MTD) of ACY 241 in combination with nivolumab.
Key Dates
- Start date
- Aug 25, 2016
- Status verified
- May 2024
- Primary completion
- Jan 22, 2024
- Completion
- Jan 22, 2024
Study Design
- Enrollment
- 17 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: ACY-241 in combination with nivolumab
Primary Outcome Measure
Number of participants with treatment-related adverse events as assessed by CTCAE v4.0 [ Time Frame: one to two years ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Local Institution - 350 | Boston | Massachusetts | 02215 | - |
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