A Study of Orally Administered JBI-802 Alone or in Combination With Pembrolizumab for Patients With Non-small Cell Lung Cancer With an STK11 Mutation.
Part of paid clinical trials in Cincinnati, Ohio.
- Sponsor
- The Christ Hospital
- Study ID
- NCT07207395
- Phase
- PHASE2
- Status
- Recruiting
Conditions
- Lung Cancer (NSCLC)
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- JBI-802 — DRUGLSD1/HDAC6 Inhibitor
- Pembrolizumab — DRUGPD-1
Study Details
The purpose of this study is to determine the overall safety and tolerability of JBI-802 as single agent and in combination with Pembrolizumab.
Key Dates
- Start date
- Apr 29, 2025
- Status verified
- Oct 2025
- Primary completion
- Oct 31, 2027
- Completion
- Oct 31, 2028
Study Design
- Enrollment
- 30 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: MonotherapyJBI-082 Single Agent
- Experimental: CombinationJBI-802 plus Pembrolizumab
Primary Outcome Measure
Incidence of Adverse Events [ Time Frame: Up to 28 days after last dose of study drug ]
Central Contacts
- Abby Reed513-585-0844
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| The Christ Hospital | Cincinnati | Ohio | 45219 | Alexander Starodub, MD, PhD (PRINCIPAL_INVESTIGATOR) |
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