Study of DSP107 and Atezolizumab for Colorectal Cancer

This study is testing if a combination of two medicines, DSP107 and atezolizumab, works better and is safer than fruquintinib for people with advanced colorectal cancer that is microsatellite stable (MSS) or mismatch repair-proficient (pMMR). These are specific types of colorectal cancer that have progressed after other treatments. You would be randomly assigned to receive either the DSP107 and atezolizumab combination or fruquintinib. Researchers will look at how long people live (overall survival) and how well the treatments work against the cancer. The goal is to find a better treatment option for this type of colorectal cancer.

Study design
This is a randomized, open-label study involving about 90 participants. You would be randomly assigned to one of two treatment groups.
What's involved
You would receive either DSP107 and atezolizumab intravenously, or fruquintinib orally, in 28-day cycles. The total time you spend in the study will depend on how you respond to treatment.
Compensation
Not stated in the trial record.
Follow-up
Researchers will track your overall survival from the first day of treatment until death, for up to 2 years.

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NCT07235293

A Study to Test DSP107 in Combination With Atezolizumab in Comparison With Fruquintinib as a New Treatment for Colorectal Cancer.

Recruiting
PHASE2Ages 18+InterventionalTreatment
Kahr Bio Australia Pty Ltd
~90 participants
Updated 2026-08-20 on ClinicalTrials.gov
What's tested:DSP107 + AtezolizumabFruquintinib

At a glance

Recruiting sites
18 of 18 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
To determine Median overall survival (mOS) in participants treated with the combination of DSP107 and atezolizumab versus fruquintinib.
Measured over From Day 1 until date of death from any cause assessed up to 2 years
Colorectal Cancer
18 sites across 11 states
Victoria5
New South Wales3
Colorado2
Florida1
North Carolina1
Pennsylvania1
Texas1
Adelaide1

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  • To determine Median overall survival (mOS) in participants treated with the combination of DSP107 and atezolizumab versus fruquintinib.From Day 1 until date of death from any cause assessed up to 2 years

    Median Overall Survival (mOS) will be estimated using Kaplan-Meier methodology as the median time from the start of study treatment to the last known date a participant was alive. Censoring rules will be applied for participants without an event at the time of analysis, and 95% confidence intervals for mOS will be provided.