A Phase 2 Platform Study of Immunomodulatory Compounds in ICI-refractory Non-small Cell Lung Cancer
Part of paid clinical trials in Houston, Texas.
- Sponsor
- M.D. Anderson Cancer Center
- Study ID
- NCT07133425
- Phase
- PHASE2
- Status
- Recruiting
Conditions
- ICI-refractory
- Non-Small Cell Lung Cancer
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- SAR445877 — DRUGGiven by IV
Study Details
To learn if SAR445877 can help to control locally advanced or metastatic NSCLC in patients who have previously received ICI therapy.
Key Dates
- Start date
- Nov 6, 2025
- Status verified
- May 2026
- Primary completion
- Feb 1, 2028
- Completion
- Feb 1, 2030
Study Design
- Enrollment
- 29 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Phase II biomarker study of SAR445877Will receive SAR445877 by vein over about 60 minutes every 2 weeks, on Day 1 of each 14-day cycle.
Primary Outcome Measure
Safety and adverse events (AEs) [ Time Frame: Through study completion; an average of 1 year ]
Central Contacts
- Natalie Vokes, MD713-303-6890
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| MD Anderson Cancer Center | Houston | Texas | 77030 | Natalie Vokes, MD (PRINCIPAL_INVESTIGATOR) |
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