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

RECRUITINGPhase 2Sponsored by Kahr Bio Australia Pty Ltd
Actively Recruiting
PhasePhase 2
SponsorKahr Bio Australia Pty Ltd
Started2026-01-20
Est. completion2026-09-30
Eligibility
Age18 Years+
Healthy vol.Accepted
Locations5 sites

Summary

This clinical study is testing whether a new combination of medicines (DSP107 and atezolizumab) is more effective and safer than an existing treatment (fruquintinib) for people with advanced colorectal cancer that is microsatellite stable (MSS). Participants will be randomly assigned to receive one of the two treatments, and researchers will monitor how well the cancer responds, how safe the treatments are, and how the body processes them. The study hopes to show that the new combination can improve outcomes for patients with this type of colorectal cancer.

Eligibility

Age: 18 Years+Healthy volunteers accepted
Inclusion Criteria:

1. Are ≥ 18 years of age with a life expectancy of \> 3 months.
2. Participants with histologically confirmed, inoperable, MSS and/or pMMR CRC which has progressed to, or is intolerant to, specified therapies (and has received prior treatment with no more than 3 lines of therapy).

   Note: Lines of therapy are defined by disease progression between therapies. Participants who discontinue their prior regimen due to toxicity (in the absence of disease recurrence/progression) will also have their prior therapy count as one prior regimen.
3. Measurable disease per RECIST v1.1.

Exclusion Criteria:

1. Central nervous system (CNS) metastases unless stable 2 months post definitive therapy with steroids.
2. Unresolved AEs of Grade 2 or higher from prior anticancer therapy.
3. Past or current history of autoimmune disease or immune deficiency.
4. History of other malignancy within 3 years of first study treatment cycle.
5. Current or recent treatment with certain therapies including specified anticancer treatments, modulators of CYP3A4 and immunomodulating therapies (prior treatment with CPIs is not exclusory).
6. Known allergy or hypersensitivity to any of the test compounds, materials, or contraindication to test product.
7. Clinically significant abnormal laboratory safety tests.

Conditions2

CancerColorectal Cancer

Locations5 sites

Colorado

1 site
University of Colarodo Cancer Center
Aurora, Colorado, 80045
Hannah Robinson

Florida

1 site
Mayo Clinic
Florida City, Florida, 32224
Conor O'Donnell, Dr

North Carolina

1 site
Duke Cancer Institute - Duke Cancer Center
Durham, North Carolina, 27710
Nicholas DeVito

Pennsylvania

1 site
UPMC Hillman Cancer Center
Pittsburgh, Pennsylvania, 15232
Anwaar Saeed, MD

Texas

1 site
The University of Texas MD Anderson Cancer Center
Texas City, Texas, 77030
Maria Pia Morelli, MD

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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.

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