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Study identifier: NCT07525206 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Study to Access Intravenous (IV) Telisotuzumab Adizutecan in Combination With IV Bevacizumab Compared to Standard of Care IV Bevacizumabin Combination With Oral Trifluridine and Tipiracil in Adult Participants With Refractory Metastatic Colorectal Cancer

Condition: Colorectal Cancer  ·  Sponsor: AbbVie

PhasePhase 3
Planned participants700
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Colorectal cancer (CRC) is the third most common type of cancer diagnosed worldwide. The purpose of this study is to assess the adverse events and change in disease activity of telisotuzumab adizutecan plus bevacizumab compared to standard of care (SOC) of LONSURF (trifluridine and tipiracil) plus bevacizumab in adult participants with c-Met over-expressed refractory metastatic colorectal cancer (mCRC). Telisotuzumab adizutecan is an investigational drug being developed for the treatment of CRC. Participants will then be randomized into 2 groups called treatment arms. One group will receive telisotuzumab adizutecan with bevacizumab in different doses. Another group will receive standard of care (SOC), trifluridine and tipiracil (LONSURF), with Bevacizumab. Up to approximately 700 adult participants with refractory mCRC, will be enrolled in the study in approximately 125 sites globally. In this Phase 3, one of two groups will receive doses of Intravenous (IV) telisotuzumab adizutecan + bevacizumab and other group will receive oral SOC of trifluridine/tipiracil (LONSURF)+ Intravenous (IV) bevacizumab. The study will run for a duration of approximately of 36 months. There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at an approved institution (hospital or clinic). The effect of the treatment will be frequently checked by medical assessments, blood tests, questionnaire…

This description comes directly from the study's public registry record.

Talk to the study team

ABBVIE CALL CENTER  ·  844-663-3742  ·  abbvieclinicaltrials@abbvie.com

Always discuss trial participation with your own doctor first.

Locations (32)

Astera Cancer Care /ID# 279532East Brunswick, New Jersey, United StatesRecruiting
Northwell Health Center for Advanced Medicine. /ID# 279590Lake Success, New York, United StatesRecruiting
Compass Oncology - Rose Quarter /ID# 280127Portland, Oregon, United StatesRecruiting
University Of Washington-Fred Hutchinson Cancer Center - Seattle /ID# 281451Seattle, Washington, United StatesRecruiting
Imelda Ziekenhuis /ID# 279333Bonheiden, Antwerpen, BelgiumRecruiting
Algemeen Ziekenhuis klina /ID# 279331Brasschaat, Antwerpen, BelgiumNot Yet Recruiting
Universitair Ziekenhuis Antwerpen /ID# 279334Edegem, Antwerpen, BelgiumRecruiting
Institut Jules Bordet /ID# 279406Anderlecht, Brussels Capital, BelgiumRecruiting
Grand Hopital de Charleroi - Les Viviers /ID# 279336Charleroi, Hainaut, BelgiumRecruiting
AZ Maria Middelares /ID# 280141Ghent, Oost-Vlaanderen, BelgiumRecruiting
AZ-Delta. /ID# 279329Roeselare, West-Vlaanderen, BelgiumRecruiting
National Cancer Center Hospital East /ID# 279917Kashiwa-shi, Chiba, JapanRecruiting

+ 20 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07525206