Summary

Eligibility
for people ages 18 years and up (full criteria)
Location
at Los Angeles, California and other locations
Dates
study started
study ends around

Description

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)

Official Title

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

Details

This trial will be performed as a phase 3, randomized, active-controlled, double-blind, multiregional study comparing Ivonescimab in combination with mFOLFOX6 (Oxaliplatin, Leucovorin and 5-Fluorouracil) versus Bevacizumab in combination with mFOLFOX6 in patients with metastatic colorectal cancer who have not previously received systemic therapy for metastatic disease. Approximately 600 patients will be randomly assigned to the 2 treatment groups in a 1:1 ratio. Each enrolled subject will receive an intravenous infusion of the Ivonescimab/Bevacizumab Plus mFOLFOX6 (Q2W, up to 8 cycles) in treatment periods per the randomization schedule. Afterward, Ivonescimab/ Bevacizumab Plus 5-Fluorouracil and Leucovorin will be used for maintenance treatment (administered on Day 1 of each cycle, Q2W) for up to 2 years.

Keywords

Metastatic Colorectal Cancer (CRC), mCRC, Ivonescimab, Colorectal Neoplasms, Oxaliplatin, Leucovorin, Fluorouracil, Bevacizumab, Drug: Ivonescimab Injection, Drug: Bevacizumab Injection

Eligibility

You can join if…

Open to people ages 18 years and up

  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 CAN'T join 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

Locations

  • Clinical Study Site accepting new patients
    Los Angeles California 90404 United States
  • Clinical Study Site accepting new patients
    Beverly Hills California 90212 United States
  • Clinical Study Site accepting new patients
    Los Angeles California 90067 United States
  • Clinical Study Site accepting new patients
    Beverly Hills California 90211 United States
  • Clinical Study Site accepting new patients
    West Hollywood California 90048 United States
  • Clinical Study Site accepting new patients
    Los Angeles California 90027 United States
  • Clinical Study Site accepting new patients
    Torrance California 90503 United States
  • Clinical Study Site accepting new patients
    Pasadena California 91030 United States
  • Clinical Study Site accepting new patients
    Cerritos California 90703 United States
  • Clinical Study Site accepting new patients
    Duarte California 91010 United States

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Summit Therapeutics
Links
Sign up for this study
ID
NCT07228832
Phase
Phase 3 research study
Study Type
Interventional
Participants
Expecting 600 study participants
Last Updated