A Study to Evaluate the Efficacy and Safety of Standard-of-Care Chemotherapy and Bevacizumab With or Without INCA33890 in the First-Line Treatment of Metastatic Microsatellite Stable Colorectal Cancer
Recruiting now Phase 3 NCT07284849
Run by Incyte Corporation · for 18 and older · All sexes
What this study is about
The purpose of this study is to evaluate the efficacy and safety of standard-of-care chemotherapy and bevacizumab with or without INCA33890 in the first-line treatment of metastatic microsatellite stable colorectal cancer.
Who can join (things the study team will check)
✅ You may be able to join if…
- Stage IV colorectal adenocarcinoma not amenable to curative resection.
- No prior systemic treatment for unresectable or metastatic disease. Participants who received adjuvant or neoadjuvant therapy may enroll if there was no recurrence within 12 months of the end of treatment.
- Measurable disease per RECIST v1.1.
- ECOG performance status of 0 or 1.
- Adequate organ function determined by laboratory results.
🚫 You may not be able to join if…
- MSI-H/dMMR per historical data in the medical record.
- BRAF V600E mutation per historical data in the medical record.
- Untreated and/or progressing CNS metastases.
- History of other malignancy within 2 years.
- Treatment with an anti-PD-(L)1 or other immune checkpoint inhibitor for any indication within the last 3 years.
- Active autoimmune disease that has required systemic treatment in the past 2 years.
- Significant concurrent and/or uncontrolled medical condition.
- History of organ transplant, including allogeneic stem cell transplantation. Other protocol-defined inclusion/exclusion criteria apply.
Where this trial is running
- Ironwood Cancer & Research Centers, Chandler, Arizona, United States
- The University of Arizona Cancer Center, Tucson, Arizona, United States
- Roche Tissue Diagnostics, Companion Diagnostics, Tucson, Arizona, United States
- Memorial Care Orange Coast Medical Center, Fountain Valley, California, United States
- Providence Medical Foundation, Fullerton, California, United States
- Cancer & Blood Research Center, Los Alamitos, California, United States
- University of California Los Angeles Health, Los Angeles, California, United States
- Sarah Cannon Research Institute Scri Oncology Partners, Aurora, Colorado, United States
- Hartford Hospital, Hartford, Connecticut, United States
- George Washington University, Washington D.C., District of Columbia, United States
- Florida Oncology & Hematology, Fort Myers, Florida, United States
- University of Florida Health, Gainesville, Florida, United States
+ 264 more sites.
Who to contact
Incyte Corporation Call Center (US) · 1.855.463.3463 · medinfo@incyte.com
It's completely normal to call and ask questions before deciding anything. Mention the study ID: NCT07284849.
Verify everything on the official ClinicalTrials.gov record. Page updated July 2026.
Beacon is an information tool, not medical advice. Whether a trial is right for you is a decision for you, your doctor, and the study team. Trial details come from the official registry, ClinicalTrials.gov, and may change — always confirm with the study team. Beacon collects no data about you: this page has no cookies, no accounts, and no tracking.