Summary

Eligibility
for people ages 18 years and up (full criteria)
Location
at UC Irvine
Dates
study started
study ends around
Principal Investigator
by Farshid Dayyani (uci)

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
    Irvine California 92612 United States
  • Clinical Study Site accepting new patients
    San Francisco California 94115 United States
  • Clinical Study Site accepting new patients
    Santa Clara California 94115 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
    Fountain Valley California 92708 United States
  • Clinical Study Site accepting new patients
    Huntington Beach California 92648 United States

Lead Scientist at University of California Health

  • Farshid Dayyani (uci)
    Clinical Professor, Medicine, School of Medicine. Authored (or co-authored) 134 research publications

Details

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