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

RecruitingPhase 3

A Randomized, Active-Controlled, Double-blind, Multicenter, Phase 3 Clinical Study of Ivonescimab in Combination With FOLFOX Versus Bevacizumab in Combination With FOLFOX for the First-line Treatment of Metastatic Colorectal Cancer

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
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

About the 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)

What is being tested

Sponsor: Summit Therapeutics · Participants: 600 · Started: Nov 18, 2025

Contact the study team

Official record on ClinicalTrials.gov — NCT07228832

Locations in the U.S.

AlabamaClinical Study Site, Mobile
Clinical Study Site, Tuscaloosa
ArizonaClinical Study Site, Goodyear
CaliforniaClinical Study Site, Beverly Hills
Clinical Study Site, Beverly Hills
Clinical Study Site, Cerritos
Clinical Study Site, Corona
Clinical Study Site, Duarte
Clinical Study Site, Fountain Valley
Clinical Study Site, Huntington Beach
Clinical Study Site, Irvine
Clinical Study Site, Irvine
Clinical Study Site, Los Angeles
Clinical Study Site, Los Angeles
Clinical Study Site, Los Angeles
Clinical Study Site, Murrieta
Clinical Study Site, Oakland
Clinical Study Site, Orange
Clinical Study Site, Pasadena
Clinical Study Site, Roseville
Clinical Study Site, San Francisco
Clinical Study Site, Santa Clara
Clinical Study Site, Stanford
Clinical Study Site, Torrance
Clinical Study Site, Upland
Clinical Study Site, Vallejo
Clinical Study Site, West Hollywood
ConnecticutClinical Study Site, Hartford
Clinical Study Site, New Haven
Clinical Study Site, Norwich
DelawareClinical Study Site, Newark
FloridaClinical Study Site, Hialeah
Clinical Study Site, Miami
Clinical Study Site, Miami Beach
Clinical Study Site, Ocala
Clinical Study Site, Orlando
Clinical Study Site, Orlando
Clinical Study Site, Plantation
Clinical Study Site, Port Saint Lucie
Clinical Study Site, St. Petersburg
Clinical Study Site, Tamarac
GeorgiaClinical Study Site, Atlanta
Clinical Study Site, Atlanta
Clinical Study Site, Newnan
IllinoisClinical Study Site, Chicago
Clinical Study Site, Elmhurst
Clinical Study Site, O'Fallon
IndianaClinical Study Site, Fort Wayne
Clinical Study Site, Indianapolis
KansasClinical Study Site, Westwood
KentuckyClinical Study Site, Edgewood
LouisianaClinical Study Site, New Orleans
MarylandClinical Study Site, Baltimore
MichiganClinical Study Site, Detroit
MinnesotaClinical Study Site, Saint Louis Park
MissouriClinical Study Site, Springfield
MontanaClinical Study Site, Billings
NebraskaClinical Study Site, Lincoln
New HampshireClinical Study Site, Lebanon
New JerseyClinical Study Site, New Brunswick
New YorkClinical Study Site, Mineola
Clinical Study Site, New York
Clinical Study Site, Rochester
Clinical Study Site, Syracuse
Clinical Study Site, The Bronx
Clinical Study Site, White Plains
North CarolinaClinical Study Site, Pinehurst
OhioClinical Study Site, Akron
Clinical Study Site, Canton
Clinical Study Site, Cincinnati
Clinical Study Site, Cincinnati
Clinical Study Site, Cleveland
Clinical Study Site, Cleveland
Clinical Study Site, Mayfield Heights
OklahomaClinical Study Site, Oklahoma City
PennsylvaniaClinical Study Site, Lebanon
Clinical Study Site, Philadelphia
Clinical Study Site, Philadelphia
Clinical Study Site, Philadelphia
Clinical Study Site, Pittsburgh
Clinical Study Site, Pittsburgh
Clinical Study Site, Sellersville
Rhode IslandClinical Study Site, Providence
South CarolinaClinical Study Site, Greenville
Clinical Study Site, Spartanburg
TennesseeClinical Study Site, Germantown
Clinical Study Site, Hermitage
TexasClinical Study Site, Dallas
Clinical Study Site, Dallas
Clinical Study Site, Fort Worth
Clinical Study Site, Houston
Clinical Study Site, Houston
Clinical Study Site, Tyler
UtahClinical Study Site, Salt Lake City
Clinical Study Site, Salt Lake City
VermontClinical Study Site, Burlington
VirginiaClinical Study Site, Charlottesville
Clinical Study Site, Fairfax
WashingtonClinical Study Site, Spokane
Clinical Study Site, Tacoma
West VirginiaClinical Study Site, Charleston
WisconsinClinical Study Site, Madison

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.