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Clinical Trials for Colon Cancer

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There are 137 active trials for advanced/metastatic colon cancer. Click on a trial to see more information.

137 trials meet filter criteria.

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Active drug More information High burden on patient More information
Sponsor: Verastem, Inc. (industry) Phase: 1/2 Start date: June 13, 2025

HealthScout AI summary: This trial enrolls adults with advanced solid tumors harboring a KRAS G12D mutation (including PDAC, NSCLC, and CRC) who have progressed after prior therapy, and evaluates the investigational oral KRAS G12D dual ON/OFF inhibitor VS-7375 as monotherapy and in combination with cetuximab. Key exclusions include prior KRAS G12D inhibitors and active CNS metastases.

ClinicalTrials.gov ID: NCT07020221

Active drug More information High burden on patient More information
Sponsor: Arvinas Inc. (industry) Phase: 1/2 Start date: May 29, 2025

HealthScout AI summary: This trial enrolls adults with advanced solid tumors or pancreatic ductal adenocarcinoma harboring a KRAS G12D mutation who have received prior standard therapies, testing ARV-806, an investigational IV protein degrader specifically targeting mutant KRAS G12D. Patients with prior KRAS G12D/pan-KRAS inhibitor exposure or uncontrolled comorbidities are excluded.

ClinicalTrials.gov ID: NCT07023731

Active drug More information High burden on patient More information
Sponsor: Qurgen Inc. (industry) Phase: 1 Start date: Sept. 19, 2023

HealthScout AI summary: Eligible adult patients with advanced, relapsed, or treatment-refractory solid tumors—including specific expansion cohorts for breast, pancreatic, ovarian, or colorectal cancer—may receive SON-DP, a first-in-class investigational protein that reprograms malignant cells into normal tissue cells rather than killing them, via IV infusion.

ClinicalTrials.gov ID: NCT05989724

Active drug More information High burden on patient More information
Sponsor: Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins (other) Phase: 1 Start date: Nov. 4, 2024

HealthScout AI summary: This trial enrolls adults with unresectable or metastatic, mismatch repair-proficient colorectal cancer or pancreatic ductal adenocarcinoma harboring vaccine-covered KRAS mutations who have progressed after first-line chemotherapy, and treats them with a mutant KRAS-targeted peptide vaccine plus balstilimab (anti-PD-1) and botensilimab (Fc-enhanced anti-CTLA-4). Immunotherapy-naive patients with measurable disease and good performance status are eligible.

ClinicalTrials.gov ID: NCT06411691

Active drug More information High burden on patient More information
Sponsor: National Cancer Institute (NCI) (federal) Phase: 1/2 Start date: Sept. 28, 2023

HealthScout AI summary: This trial enrolls adults with advanced metastatic solid tumors—particularly those with MGMT promoter hypermethylation or for whom temozolomide is standard therapy—and evaluates the combination of oral temozolomide with tuvusertib (M1774), a selective ATR kinase inhibitor that targets the DNA damage response pathway. The phase 2 focus is on patients with mismatch repair proficient/microsatellite stable colorectal cancer with MGMT promoter hypermethylation.

ClinicalTrials.gov ID: NCT05691491

Active drug More information High burden on patient More information
Sponsor: Revolution Medicines, Inc. (industry) Phase: 1/2 Start date: May 24, 2024

HealthScout AI summary: This trial enrolls adults with metastatic or unresectable, RAS-mutant colorectal or pancreatic cancer (including KRAS G12D subsets), and tests oral RAS(ON) inhibitors—RMC-6236 (a multi-selective tri-complex RAS inhibitor) and RMC-9805 (a KRAS G12D-selective molecular glue)—either as monotherapy or combined with standard therapies such as mFOLFOX6, mFOLFIRINOX, gemcitabine/nab-paclitaxel, bevacizumab, or cetuximab. All patients must have ECOG 0-1 and adequate organ function.

ClinicalTrials.gov ID: NCT06445062

Active drug More information High burden on patient More information
Sponsor: National Cancer Institute (NCI) (federal) Phase: 1 Start date: Nov. 8, 2023

HealthScout AI summary: This trial enrolls adults with metastatic or unresectable solid tumors—including those with prior exposure to fluorouracil or capecitabine—to receive the BET bromodomain inhibitor ZEN003694 (which disrupts BRD4-mediated oncogenic transcription) in combination with capecitabine. Expansion cohorts specifically include metastatic colorectal cancer.

ClinicalTrials.gov ID: NCT05803382

Active drug More information High burden on patient More information
Sponsor: David Wald (other) Phase: 1 Start date: Sept. 9, 2022

HealthScout AI summary: This trial enrolls adults with locally advanced/metastatic colorectal, gastric, or esophageal cancer, or relapsed/refractory hematologic malignancies who have progressed on standard therapies or are ineligible, and treats them with fludarabine/cyclophosphamide lymphodepletion followed by ex vivo expanded universal donor NK cell infusions combined with low-dose IL-2 and vactosertib, a TGFβ receptor I (ALK5) inhibitor designed to enhance NK cell activity by blocking TGFβ-mediated immunosuppression.

ClinicalTrials.gov ID: NCT05400122

Active drug More information High burden on patient More information
Sponsor: National Cancer Institute (NCI) (federal) Phase: 1 Start date: June 5, 2024

HealthScout AI summary: This trial enrolls adults with refractory, BRAF V600E-mutant metastatic colorectal cancer who have previously tolerated encorafenib plus cetuximab, and evaluates the addition of ZEN003694, a pan-BET bromodomain inhibitor, to ongoing encorafenib and cetuximab therapy. Patients must have good performance status and adequate organ function, and may have stable or treated brain metastases.

ClinicalTrials.gov ID: NCT06102902

Active drug More information High burden on patient More information
Sponsor: University of Southern California (other) Phase: 1 Start date: Jan. 15, 2025

HealthScout AI summary: This trial enrolls adults with microsatellite stable, KRAS-mutant metastatic colorectal cancer who have progressed on or are intolerant of standard chemotherapy, and excludes those with diabetes or prior anti-PD1/CTLA-4 therapy. Patients receive combination therapy with botensilimab (Fc-engineered anti-CTLA-4 antibody), balstilimab (anti-PD-1 antibody), a fasting-mimicking diet, and high-dose intravenous vitamin C.

ClinicalTrials.gov ID: NCT06336902

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