Phase III Study of Ivonescimab or Bevacizumab Combined With FOLFOX in Patients With Metastatic Colorectal Cancer
Start Date
11/18/2025
Completion Date
11/30/2029
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)
Detailed Description
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.
Eligibility Criteria
Age Range: 18 years to No maximum
Interventions
Drug: Ivonescimab Injection
Drug: Bevacizumab Injection
Conditions
Locations
Clinical Study Site
Mobile, Alabama 36604
United States
Clinical Study Site
Tuscaloosa, Alabama 35487
United States
Clinical Study Site
Goodyear, Arizona 85338
United States
Clinical Study Site
Beverly Hills, California 90211
United States
Clinical Study Site
Beverly Hills, California 90212
United States
Clinical Study Site
Cerritos, California 90703
United States
Clinical Study Site
Corona, California 92882
United States
Clinical Study Site
Duarte, California 91010
United States
Clinical Study Site
Fountain Valley, California 92708
United States
Clinical Study Site
Huntington Beach, California 92648
United States
Clinical Study Site
Irvine, California 92612
United States
Clinical Study Site
Irvine, California 92618
United States
Clinical Study Site
Los Angeles, California 90027
United States
Clinical Study Site
Los Angeles, California 90067
United States
Clinical Study Site
Los Angeles, California 90404
United States
Clinical Study Site
Murrieta, California 92562
United States
Clinical Study Site
Orange, California 92868
United States
Clinical Study Site
Pasadena, California 91030
United States
Clinical Study Site
Torrance, California 90503
United States
Clinical Study Site
Upland, California 91786
United States
Clinical Study Site
West Hollywood, California 90048
United States
Clinical Study Site
Hartford, Connecticut 06106
United States
Clinical Study Site
New Haven, Connecticut 06520-8028
United States
Clinical Study Site
Norwich, Connecticut 06360
United States
Clinical Study Site
Newark, Delaware 19713
United States
Clinical Study Site
Hialeah, Florida 33013
United States
Clinical Study Site
Miami, Florida 33176
United States
Clinical Study Site
Orlando, Florida 32806
United States
Clinical Study Site
Plantation, Florida 33322
United States
Clinical Study Site
Port Saint Lucie, Florida 34952
United States
Clinical Study Site
St. Petersburg, Florida 33705
United States
Clinical Study Site
Tamarac, Florida 33321
United States
Clinical Study Site
Atlanta, Georgia 30303
United States
Clinical Study Site
Atlanta, Georgia 30322
United States
Clinical Study Site
Newnan, Georgia 30265
United States
Clinical Study Site
Chicago, Illinois 60611
United States
Clinical Study Site
Elmhurst, Illinois 60540
United States
Clinical Study Site
O'Fallon, Illinois 62269
United States
Clinical Study Site
Fort Wayne, Indiana 46804
United States
Clinical Study Site
Indianapolis, Indiana 46202
United States
Clinical Study Site
Westwood, Kansas 66205
United States
Clinical Study Site
Edgewood, Kentucky 41017
United States
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New Orleans, Louisiana 70121
United States
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Baltimore, Maryland 21201
United States
Clinical Study Site
Detroit, Michigan 48201
United States
Clinical Study Site
Saint Louis Park, Minnesota 55426
United States
Clinical Study Site
Springfield, Missouri 65804
United States
Clinical Study Site
Billings, Montana 59102
United States
Clinical Study Site
Lincoln, Nebraska 68506
United States
Clinical Study Site
Lebanon, New Hampshire 03766
United States
Clinical Study Site
New Brunswick, New Jersey 08901
United States
Clinical Study Site
Mineola, New York 11501
United States
Clinical Study Site
New York, New York 10016
United States
Clinical Study Site
Rochester, New York 14642
United States
Clinical Study Site
Syracuse, New York 13210
United States
Clinical Study Site
The Bronx, New York 10461
United States
Clinical Study Site
White Plains, New York 10601-5000
United States
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Akron, Ohio 44032
United States
Clinical Study Site
Canton, Ohio 44703
United States
Clinical Study Site
Cincinnati, Ohio 45219
United States
Clinical Study Site
Cincinnati, Ohio 45220
United States
Clinical Study Site
Cleveland, Ohio 44111
United States
Clinical Study Site
Cleveland, Ohio 44195
United States
Clinical Study Site
Mayfield Heights, Ohio 44124
United States
Clinical Study Site
Oklahoma City, Oklahoma 73120
United States
Clinical Study Site
Lebanon, Pennsylvania 17042
United States
Clinical Study Site
Philadelphia, Pennsylvania 19111
United States
Clinical Study Site
Philadelphia, Pennsylvania 19140
United States
Clinical Study Site
Pittsburgh, Pennsylvania 15212
United States
Clinical Study Site
Providence, Rhode Island 02903
United States
Clinical Study Site
Greenville, South Carolina 29605
United States
Clinical Study Site
Hermitage, Tennessee 37129
United States
Clinical Study Site
Dallas, Texas 75235
United States
Clinical Study Site
Dallas, Texas 75390
United States
Clinical Study Site
Fort Worth, Texas 76104
United States
Clinical Study Site
Tyler, Texas 75701
United States
Clinical Study Site
Salt Lake City, Utah 84106
United States
Clinical Study Site
Charlottesville, Virginia 22908
United States
Clinical Study Site
Fairfax, Virginia 22031
United States
Clinical Study Site
Spokane, Washington 99208
United States
Clinical Study Site
Tacoma, Washington 98405
United States
Clinical Study Site
Charleston, West Virginia 25304
United States
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Madison, Wisconsin 53792
United States
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Brussels, 1000
Belgium
Clinical Study Site
Ghent, 9000
Belgium
Clinical Study Site
Haine-Saint-Paul, 7100
Belgium
Clinical Study Site
Kortrijk, 8500
Belgium
Clinical Study Site
Toronto, Ontario M4N 3M5
Canada
Clinical Study Site
Montreal, Quebec H4A 3J1
Canada
Clinical Study Site
Regina, Saskatchewan S4T7T1
Canada
Clinical Study Site
Hradec Králové, 50005
Czechia
Clinical Study Site
Prague, 14059
Czechia
Clinical Study Site
Lyon, 69374
France
Clinical Study Site
Montpellier, 34298
France
Clinical Study Site
Nantes, 44000
France
Clinical Study Site
Paris, 75015
France
Clinical Study Site
Paris, 75020
France
Clinical Study Site
Pierre-Bénite, 69495
France
Clinical Study Site
Poitiers, 86000
France
Clinical Study Site
Strasbourg, 67033
France
Clinical Study Site
Bonn, 53113
Germany
Clinical Study Site
Hamburg, 20249
Germany
Clinical Study Site
Hamburg, 22763
Germany
Clinical Study Site
Meldola, 47014
Italy
Clinical Study Site
Osaka, Ontario 565-0871
Japan
Clinical Study Site
Aichi, 464-8681
Japan
Clinical Study Site
Chiba, 260-8717
Japan
Clinical Study Site
Ehime, 791-0280
Japan
Clinical Study Site
Fukuoka, 812-8582
Japan
Clinical Study Site
Gifu, 501-1194
Japan
Clinical Study Site
Hiroshima, 734-8551
Japan
Clinical Study Site
Hokkaido, 060-8648
Japan
Clinical Study Site
Kawasaki, 216-8511
Japan
Clinical Study Site
Osaka, 541-8567
Japan
Clinical Study Site
Saitama, 362-0806
Japan
Clinical Study Site
Sendai, 980-0872
Japan
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Shizuoka, 411-8777
Japan
Clinical Study Site
Tokyo, 104-0045
Japan
Clinical Study Site
Tokyo, 135-8550
Japan
Clinical Study Site
Toyama, 930-0194
Japan
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Yokohama, 241-8515
Japan
Clinical Study Site
Rzeszów, Podkarpackie Voivodeship 35-021
Poland
Clinical Study Site
Warsaw, 04-141
Poland
Clinical Study Site
Rio Piedras, 00935
Puerto Rico
Clinical Study Site
A Coruña, 15006
Spain
Clinical Study Site
Barcelona, 08035
Spain
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Barcelona, 08908
Spain
Clinical Study Site
Madrid, 28009
Spain
Clinical Study Site
Madrid, 28046
Spain
Clinical Study Site
Madrid, 28050
Spain
Clinical Study Site
Palma de Mallorca, 07198
Spain
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Santander, 39008
Spain
Clinical Study Site
Valencia, 46010
Spain
Clinical Study Site
Valencia, 46014
Spain
Clinical Study Site
Valencia, 46026
Spain
Clinical Study Site
Canterbury, England CT13NS
United Kingdom
Clinical Study Site
London, England EC1M 6BQ
United Kingdom
Clinical Study Site
Aberdeen, Scotland AB25 2ZN
United Kingdom
Clinical Study Site
Edinburgh, EH4 2XU
United Kingdom
Clinical Study Site
Manchester, M20 4BX
United Kingdom