TTrialPathMatch Me to Trials
← Back to trials
RecruitingMetastatic Colorectal Cancer (CRC)

Phase III Study of Ivonescimab or Bevacizumab Combined With FOLFOX in Patients With Metastatic Colorectal Cancer

Eligible age

18+ yrs

Accepts

All genders

Locations

33 states

Healthy volunteers

No

See if you qualify for this study

Answer a few quick questions about your location and health. Takes about a minute.

Check my eligibility →

About this study

A Randomized, Active-Controlled, Double-blind, Multicenter, Phase 3 Clinical Study of Ivonescimab in Combination with mFOLFOX6 (Oxaliplatin, Leucovorin and 5-Fluorouracil) versus Bevacizumab in Combination with FOLFOX for the First-line Treatment of Metastatic Colorectal Cancer(HARMONi-GI3)

Sponsor: Summit Therapeutics

You may qualify if…

  • 1. ECOG performance status score of 0 or 1
  • 2. Expected life expectancy ≥ 6 months
  • 3. Patients with histologically or cytologically confirmed metastatic CRC
  • 4. No prior systemic therapy for metastatic CRC
  • 5. At least 1 measurable noncerebral lesion

You may not qualify if…

  • 1. Microsatellite instability-high (MSI-H) or mismatch repair deficient (dMMR) disease
  • 2. Known BRAF V600E mutant status
  • 3. Current presence of significant radiographic or clinical manifestations of gastrointestinal (GI) obstruction
  • 4. Ascites requiring paracentesis within last 30 days
  • 5. Patients who have received prior immunotherapy or anti-angiogenic therapy for colorectal cancer
  • 6. Active or prior history of inflammatory bowel disease (eg, Crohn's disease, ulcerative colitis, or chronic diarrhea)
  • 7. Resectable disease

Where it's recruiting

Alabama

Mobile · Tuscaloosa

Arizona

Goodyear

California

Beverly Hills · Cerritos · Corona · Duarte

Connecticut

Hartford · New Haven · Norwich

Delaware

Newark

Florida

Hialeah · Miami · Miami Beach · Ocala

Georgia

Atlanta · Newnan

Illinois

Chicago · Elmhurst · O'Fallon

Indiana

Fort Wayne · Indianapolis

Kansas

Westwood

Kentucky

Edgewood

Louisiana

New Orleans

Source: ClinicalTrials.gov · NCT07228832 · last updated 2026-08-04