A Randomized Open-Label Phase 2 Study of a Patient-Specific Vaccine Targeting Neoantigens in Combination with Immune Checkpoint Blockade for Patients with Colon Cancer with Minimal Residual Disease Following Surgical Resection and Standard Adjuvant Chem

Brief description of study

The purpose of the study is to determine the safety and effectiveness of the patient-specific-vaccine targeting neoantigens in combination with immune checkpoint blockade for patients with colon cancer. We will characterize the antitumor activity of adjuvant treatment with GRT-C901/GRT-R902 in combination with checkpoint inhibitors based on molecular response. The vaccine has not been approved by the U.S Food and Drug Administration (FDA), the health authority that gives approval for new agents to be prescribed in the United States, but the FDA has given its permission to test this agent in the current trial.

Clinical Study Identifier: s21-01701
ClinicalTrials.gov Identifier: NCT05456165

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