A Study of BMS-986490 With or Without Bevacizumab in Advanced Solid Tumors
Recruiting now · Phase 1/Phase 2
Conditions studied: Advanced Solid Tumors
In brief
This is a study of BMS-986490 as a monotherapy and in combination with bevacizumab in participants with select advanced solid tumors known to express CEACAM5.
Key facts
- Study ID
- NCT06730750
- Run by
- Bristol-Myers Squibb
- People needed
- 360
- Starts
- 2025-02-12
- Expected to finish
- 2029-12-09
- Last updated by the study team
- 2026-07-02
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Documented histologically or cytologically confirmed, advanced, unresectable/metastatic solid tumor measurable by RECIST v1.1.
- CRC: Part 1A, Part 2A-CRC, Part 1B, and Part 2B:
- i) Locally advanced/metastatic, recurrent, or unresectable CRC with adenocarcinoma histology and whose disease has progressed after systemic cancer therapy in the metastatic or adjuvant setting including 5-FU, irinotecan, and/or oxaliplatin (if available and not contraindicated).
- NSCLC: Part 2A-NSCLC/GC, 2L+ NSCLC:
- i) Histologically confirmed NSCLC meeting stage criteria for Stage IIIB, Stage IV, or recurrent disease.
- ii) Participants must have received and progressed on or after anti-PD-(L)1 therapy, if available.
- GC: Part 2A-NSCLC/GC, 2L+ GC: i) Participants must have received and then progressed or been intolerant to at least 1 standard treatment regimen in the advanced or metastatic setting (or have progressed within 6 months of adjuvant therapy).
- ii) ECOG performance status of 0 or 1.
You may not qualify if…
- History of anaphylactic reactions to irinotecan and/or bevacizumab.
- Previously received therapy targeting CEACAM5.
- Grade ≥3 ILD/pneumonitis.
- Other protocol-defined Inclusion/Exclusion criteria apply.
Where it is running
- Tasman Oncology Research — Southport, Queensland, Australia (enrolling)
- Princess Margaret Cancer Centre — Toronto, Ontario, Canada (enrolling)
- Local Institution - 0007 — Los Angeles, California, United States
- Local Institution - 0017 — Grand Rapids, Michigan, United States
- Local Institution - 0004 — Hackensack, New Jersey, United States
- Local Institution - 0006 — Pittsburgh, Pennsylvania, United States
Full record on ClinicalTrials.gov
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