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Clinical Trials in the UK / NCT07228832
Recruiting Phase 3

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

NCT07228832 · tracked via the Priya Life Science UK tracker
Sponsor
Summit Therapeutics
Phase
Phase 3
Started
2025-11-18
Last updated
2026-09-08

Condition(s) studied

Metastatic Colorectal Cancer (CRC)

Investigational drug(s) / intervention(s)

Drug: Ivonescimab InjectionDrug: Bevacizumab Injection

Drug: Ivonescimab Injection: Subjects will receive Ivonescimab Plus mFOLFOX6 (Oxaliplatin, Leucovorin and 5-Fluorouracil) via intravenous infusion (IV) Q2W, up to 8 cycles. Afterward, Ivonescimab plus Leucovorin and 5-Fluorouracil will be used for maintenance treatment (administered on Day 1 of each cycle, Q2W) for up to 2 years.

Drug: Bevacizumab Injection: Subjects will receive bevacizumab Plus mFOLFOX6 (Oxaliplatin, Leucovorin and 5-Fluorouracil) via intravenous infusion (IV) Q2W, up to 8 cycles in treatment periods per the randomization schedule. Afterward, bevacizumab Plus 5-FU and Leucovorin will be used for maintenance treatment (administered on Day 1 of each cycle, Q2W) up to 2 years.

Study summary

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)

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: 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 Exclusion Criteria: 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

Primary outcome measure(s)

Trial sites (213)

FacilityCityRegionStatus
Clinical Study Site Mobile Alabama Recruiting
Clinical Study Site Tuscaloosa Alabama Recruiting
Clinical Study Site Goodyear Arizona Recruiting
Clinical Study Site Beverly Hills California Recruiting
Clinical Study Site Beverly Hills California Recruiting
Clinical Study Site Cerritos California Recruiting
Clinical Study Site Corona California Recruiting
Clinical Study Site Duarte California Recruiting
Clinical Study Site Fountain Valley California Recruiting
Clinical Study Site Huntington Beach California Recruiting
Clinical Study Site Irvine California Recruiting
Clinical Study Site Irvine California Recruiting
Clinical Study Site Los Angeles California Recruiting
Clinical Study Site Los Angeles California Recruiting
Clinical Study Site Los Angeles California Recruiting
Clinical Study Site Murrieta California Recruiting
Clinical Study Site Oakland California Recruiting
Clinical Study Site Orange California Recruiting
Clinical Study Site Pasadena California Recruiting
Clinical Study Site Roseville California Recruiting
Clinical Study Site San Francisco California Recruiting
Clinical Study Site Santa Clara California Recruiting
Clinical Study Site Stanford California Recruiting
Clinical Study Site Torrance California Recruiting
Clinical Study Site Upland California Recruiting
Clinical Study Site Vallejo California Recruiting
Clinical Study Site West Hollywood California Recruiting
Clinical Study Site Hartford Connecticut Recruiting
Clinical Study Site New Haven Connecticut Recruiting
Clinical Study Site Norwich Connecticut Recruiting
Clinical Study Site Newark Delaware Recruiting
Clinical Study Site Hialeah Florida Recruiting
Clinical Study Site Miami Florida Recruiting
Clinical Study Site Miami Beach Florida Recruiting
Clinical Study Site Ocala Florida Recruiting
Clinical Study Site Orlando Florida Recruiting
Clinical Study Site Orlando Florida Recruiting
Clinical Study Site Plantation Florida Recruiting
Clinical Study Site Port Saint Lucie Florida Recruiting
Clinical Study Site St. Petersburg Florida Recruiting

+ 173 more sites — see the full list on the official registry below.

More Summit Therapeutics trials in the UK

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07228832 on ClinicalTrials.gov ↗ ← All trials in the UK