Mismatch Repair Deficiency

9

Review clinical trials related to Mismatch Repair Deficiency. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Toripalimab Plus Celecoxib for dMMR/MSI-H Locally Advanced Colorectal Cancer

The PICC-3 study is a multicentre, single-arm, phase II trial evaluating toripalimab plus celecoxib in patients with mismatch repair-deficient (dMMR) or microsatellite instability-high (MSI-H) locally advanced colorectal cancer. The trial uses a response-adapted treatment strategy, whereby patients with clinical complete response (cCR) after therapy may enter a non-operative management pathway, while patients without cCR proceed to surgery. Response assessment is based on imaging, endoscopy, biopsy evaluation, and ctDNA analysis.

Participants needed: 105
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Sun Yat-sen UniversityUpdated: May 22, 2026Locations: 1
Eligibility criteria

Signed informed consent and willingness/compliance with study procedures. [+9]

Presence of distant metastases (M1) confirmed by CT/MRI or PET-CT (at least cove... [+17]

Status: Recruiting

A Study of Oral 7HP349 (Alintegimod) in Combination With Ipilimumab Followed by Nivolumab Monotherapy

This study is an open-label Phase Ib (Part A) dose escalation followed by a blinded, randomized, multi cohort Phase 2a (Part B) comparison of combination vs. reference regimens. Currently study will only be enrolling the Phase 1b and the Phase 2a protocol requirements will be added to the study near completion of the Phase 1b

Participants needed: 126
Trial details
Phase: Phase 1, Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: 7 Hills Pharma, LLCUpdated: Apr 13, 2026Locations: 5
Eligibility criteria

Adult patients (age 18 or older) [+47]

Status: Recruiting

Liquid Biopsy and Machine Learning for Early Colorectal Cancer, Adenomas, Lynch Cancers, and Residual Disease Detection

This is an multicenter study that will test the diagnostic accuracy of a blood test (i.e., a liquid biopsy) for the diagnosis of colorectal cancer (CRC), advanced adenomas (AAs), as well as Lynch-syndrome associated cancers. Additionally, a pre-planned analysis will evaluate the use of this liquid biopsy as a tool for molecular residual disease monitoring purposes.

Participants needed: 1,200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: San Raffaele UniversityUpdated: Mar 4, 2026Locations: 4
Eligibility criteria

All individuals included in the study need to have had a colonoscopy at the time... [+2]

Lack of informed consent [+1]

Status: Not yet recruiting

Pilot Study of Navigated Focused Ultrasound and Pembrolizumab in the Treatment of Recurrent WHO Grade 4 IDH-Wildtype Glioblastoma With Mismatch Repair Deficiency

Navigated Focused Ultrasound and Pembrolizumab in the Treatment of Recurrent WHO Grade 4 IDH-Wildtype Glioblastoma with Mismatch Repair Deficiency.

Participants needed: 8
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Jennifer LeddonUpdated: Feb 4, 2026Locations: 1
Eligibility criteria

Patient previously diagnosed with WHO grade 4 IDH-wildtype GBM, determined throu... [+8]

Multifocal or leptomeningeal disease observed at the time of GBM recurrence. [+9]

Status: Not yet recruiting

Immunotherapy for Surgery Avoidance in Vulnerable dMMR Endometrial Cancer

Efficacy evaluate of iparomlimab and tuvonralimab (a PD-1/CTLA-4 bispecific antibody) in patients with surgically resectable dMMR endometrial cancer.

Participants needed: 30
Trial details
Phase: Phase 2Age: 18+Biological sex: FemaleType: InterventionalSponsor: Women's Hospital School Of Medicine Zhejiang UniversityUpdated: Jan 27, 2026
Eligibility criteria

Age:18 years or older. [+4]

Myocardial infarction; [+4]

Status: Recruiting

SYNERGY-AI: Artificial Intelligence Based Precision Oncology Clinical Trial Matching and Registry

International registry for cancer patients evaluating the feasibility and clinical utility of an Artificial Intelligence-based precision oncology clinical trial matching tool, powered by a virtual tumor boards (VTB) program, and its clinical impact on pts with advanced cancer to facilitate clinical trial enrollment (CTE), as well as the financial impact, and potential outcomes of the intervention.

Participants needed: 50,000
Trial details
Biological sex: AllType: ObservationalSponsor: Massive Bio, Inc.Updated: Oct 28, 2025Locations: 68Duration: 36 Months
Eligibility criteria

Pts with solid and hematological malignancies; [+2]

ECOG PS > 2; [+2]

Status: Recruiting

Neoadjuvant Immunotherapy for T4 dMMR Colon Cancer

Due to dMMR colon cancer patients respond poorly to conventional chemotherapy, but immunotherapy can significantly improve the pCR in this group of patients, this study intends to explore whether neoadjuvant immunotherapy can improve the R0 resection rate with preservation of adjacent organs in T4 colon cancer patients with dMMR.

Participants needed: 18
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Peking Union Medical College HospitalUpdated: Sep 5, 2025Locations: 2
Eligibility criteria

Aged 18-75 years; [+8]

A history of other malignant tumors (other than cured basal cell carcinoma, cerv... [+5]

Status: Not yet recruiting

PD-1 Inhibitor Combined With Progesterone Treatment in FST for Patients With MMRd Endometrial Cancer

The objective of this study was to investigate the feasibility of a PD-1 inhibitor in combination with progesterone as a means of preserving fertility in patients with early-stage mismatch repair-deficient (MMRd) endometrial cancer who wish to preserve fertility.

Participants needed: 10
Trial details
Age: 18-45Biological sex: FemaleType: InterventionalSponsor: Peking University People's HospitalUpdated: Aug 12, 2024Locations: 1
Eligibility criteria

Be between the ages of 18-45 years old; [+5]

Stage IB(FIGO 2009) and above; [+4]

Status: Recruiting

Perioperative Chemotherapy Plus Toripalimab for dMMR Locally Advanced Gastric or Esophagogastric Junction Adenocarcinoma

This study is a prospective, multi-center, randomized controlled phase II trial to compare the efficacy of perioperative SOX plus toripalimab, toripalimab monotherapy with SOX regimen in participants with dMMR locally advanced gastric or esophagogastric junction adenocarcinoma

Participants needed: 90
Trial details
Phase: Phase 2Age: 18-80Biological sex: AllType: InterventionalSponsor: Yu jirenUpdated: Jul 25, 2023Locations: 8
Eligibility criteria

Voluntary participation in the clinical study; fully understands and is informed... [+14]

HER2-positive status defined as either IHC score of 3+ or IHC 2+ with amplificat... [+16]