Phase 1 Study of SAR445877 for Metastatic Colorectal Cancer

This study is testing a new combination of medicines for people with metastatic colorectal cancer that is microsatellite stable (MSS). Researchers want to see if SAR445877, when given with FOLFOX6 and bevacizumab, is safe and tolerable as a first treatment. The main goal is to find the safest dose of SAR445877 in this combination. This study is open to adults aged 18 and older who are willing to follow the study plan. The study is currently unclear on its recruitment status and plans to enroll 41 participants. Success will be measured by how safe the treatment is and any side effects experienced.

Study design
This is a Phase 1 interventional study, meaning it's an early-stage trial focused on safety. It plans to enroll 41 participants.
What's involved
You would need to understand and sign an informed consent form, and be willing to attend scheduled visits, follow treatment plans, and complete laboratory tests and other study procedures.
Compensation
Not stated in the trial record.
Follow-up
Safety and adverse events will be measured through study completion, which is an average of 1 year.

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NCT07500298

Phase 1 Study Of SAR445877 In Combination With FOLFOX6 And Bevacizumab As First-Line Treatment For Microsatellite Stable Metastatic Colorectal Cancer

Recruiting
PHASE1Ages 18+InterventionalTreatment
M.D. Anderson Cancer Center
~41 participants
Updated 2026-07-23 on ClinicalTrials.gov
What's tested:SAR445877FOLFOX6Bevacizumab

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Safety and adverse events (AEs)
Measured over Through study completion; an average of 1 year.
Phase 1
SAR445877
FOlfox6
Bevacizimab
First Line Treatment
Metastatic Colorectal Cancer (CRC)
Microsatellite Stable
1 sites across 1 states
Texas1
  • Aung Naing, MD · PRINCIPAL_INVESTIGATOR · M.D. Anderson Cancer Center

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  • Safety and adverse events (AEs)Through study completion; an average of 1 year.

    Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0