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Clinical Trials for Rectal Cancer

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There are 194 active trials for advanced/metastatic rectal cancer.

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194 trials meet filter criteria.

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No known activity More information High burden on patient More information
Sponsor: TheRas, Inc., d/b/a BridgeBio Oncology Therapeutics (industry) Phase: 1 Start date: March 31, 2025

HealthScout AI summary: Adults with advanced, unresectable or metastatic solid tumors (including NSCLC, pancreatic, colorectal, or other types) harboring KRAS mutations (G12A, G12C, G12D, G12S, G12V) or amplification are eligible for treatment with BBO-11818, a selective oral pan-KRAS inhibitor, as monotherapy or in combination with pembrolizumab, platinum-based chemotherapy plus pemetrexed, or cetuximab.

ClinicalTrials.gov ID: NCT06917079

No known activity More information High burden on patient More information
Sponsor: TheRas, Inc., d/b/a BridgeBio Oncology Therapeutics (industry) Phase: 1 Start date: Oct. 29, 2024

HealthScout AI summary: This trial enrolls adults with advanced solid tumors—including HER2-positive or hormone receptor-positive/HER2-negative breast cancer, KRAS-mutant colorectal cancer, or KRAS-mutant non-small cell lung cancer—who have received prior standard therapies, to receive BBO-10203 (a first-in-class PI3Kα:RAS interaction breaker that disrupts PI3Kα-AKT signaling) as monotherapy or in combination with trastuzumab. Key exclusions include untreated brain metastases and extensive prior ADC exposure in HER2+ breast cancer.

ClinicalTrials.gov ID: NCT06625775

No known activity More information High burden on patient More information
Sponsor: Tyligand Pharmaceuticals (Suzhou) Limited (industry) Phase: 1/2 Start date: April 29, 2024

HealthScout AI summary: Eligible patients are adults with locally advanced or metastatic solid tumors harboring a KRAS G12D mutation, who have progressed on or are intolerant to standard therapies and meet organ function and performance status criteria. The investigational drug TSN1611, an oral small molecule inhibitor targeting both active and inactive forms of KRAS G12D, is administered as monotherapy.

ClinicalTrials.gov ID: NCT06385925

No known activity More information High burden on patient More information
Sponsor: Immunitas Therapeutics (industry) Phase: 1/2 Start date: Nov. 28, 2022

HealthScout AI summary: This trial enrolls adults with advanced or metastatic solid tumors or designated lymphomas (with confirmed CD161 expression) who have failed or are intolerant to standard therapies, to receive the investigational anti-CD161 monoclonal antibody IMT-009 (which blocks an inhibitory NK/T cell pathway) as monotherapy or in combination with fruquintinib.

ClinicalTrials.gov ID: NCT05565417

No known activity More information High burden on patient More information
Sponsor: Pfizer (industry) Phase: 1 Start date: Dec. 10, 2024

HealthScout AI summary: This trial enrolls adults with advanced or metastatic solid tumors harboring documented KRAS mutations (excluding prior G12C inhibitor-treated G12C tumors), including NSCLC, CRC, pancreatic, and other KRAS-mutated cancers, who have progressed after standard therapies. Patients receive PF-07985045, a novel oral KRAS inhibitor, as monotherapy or in combination with chemotherapy, targeted agents, or immunotherapy, depending on cohort and tumor type.

ClinicalTrials.gov ID: NCT06704724

No known activity More information High burden on patient More information
Sponsor: AstraZeneca (industry) Phase: 1 Start date: Dec. 22, 2022

HealthScout AI summary: This trial enrolls adults with advanced or metastatic solid tumors—including specific cohorts for EGFR-mutant or wild-type NSCLC, HNSCC, and metastatic CRC—to investigate AZD9592, a bispecific antibody-drug conjugate targeting EGFR and cMET, given alone or in combination with standard therapies such as osimertinib or 5-FU/bevacizumab/leucovorin. Key exclusions are active ILD/pneumonitis, untreated or unstable brain metastases, active infections, or significant cardiac disease.

ClinicalTrials.gov ID: NCT05647122

No known activity More information High burden on patient More information
Sponsor: Ikena Oncology (industry) Phase: 1 Start date: Dec. 18, 2023

HealthScout AI summary: This trial enrolls adults with advanced, unresectable, or metastatic solid tumors harboring RAS or RAF pathway alterations (including mutations or fusions in KRAS, NRAS, BRAF, CRAF, or NF1) who have progressed after or are intolerant to standard therapies, to receive IK-595, an investigational oral dual MEK/RAF inhibitor designed to inactivate MEK and RAF signaling.

ClinicalTrials.gov ID: NCT06270082

No known activity More information High burden on patient More information
Sponsor: AstraZeneca (industry) Phase: 1/2 Start date: Oct. 18, 2024

HealthScout AI summary: Eligible patients are adults with advanced or metastatic solid tumors harboring a KRASG12D mutation (including NSCLC, colorectal, and pancreatic cancers) who have progressed on standard therapy and have not previously received a direct KRAS inhibitor. The trial evaluates AZD0022, a selective oral KRAS G12D inhibitor, as monotherapy and in combination with cetuximab.

ClinicalTrials.gov ID: NCT06599502

No known activity More information High burden on patient More information
Sponsor: Incyte Corporation (industry) Phase: 1 Start date: Jan. 4, 2024

HealthScout AI summary: Adult patients with advanced or metastatic solid tumors harboring a KRAS G12D mutation (including pancreatic, colorectal, or NSCLC), ECOG 0-1, and no prior KRAS G12D inhibitor exposure are eligible for treatment with INCB161734, a selective oral KRAS G12D inhibitor, given alone or in combination with standard therapies (e.g., gemcitabine/nab-paclitaxel, mFOLFIRINOX, cetuximab, or retifanlimab).

ClinicalTrials.gov ID: NCT06179160

No known activity More information High burden on patient More information
Sponsor: Seagen, a wholly owned subsidiary of Pfizer (industry) Phase: 1 Start date: Nov. 14, 2023

HealthScout AI summary: This trial enrolls adults with advanced, unresectable or metastatic colorectal cancer, non-small cell lung cancer, non-nasopharyngeal head and neck squamous cell carcinoma, or pancreatic ductal adenocarcinoma who have progressed on or are intolerant to standard therapies. Patients will receive PF-08046052/SGN-EGFRd2, a bispecific antibody that targets EGFR and conditionally activates γ9δ2-T cells to promote anti-tumor immune responses.

ClinicalTrials.gov ID: NCT05983133

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