SMARCA4 Gene Mutation: Clinical Trials

3 trials for SMARCA4 Gene Mutation, newest first

ClinicalTrials Daily  ·  Areas  ·  Conditions  ·  Drugs  ·  Sponsors  ·  

1 completed, 1 recruiting, 1 terminated. 1 Phase 1, 1 Phase 2.

By phase and status

PhaseTrialsStatus
Phase 11Completed 1
Phase 21Terminated 1

Follow SMARCA4 Gene Mutation: new trials by email Literature Review of SMARCA4 Gene Mutation trials Research Report on SMARCA4 Gene Mutation

Trials newest first · largest first

Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.

TrialPhaseStatusSponsorEnrollmentStartUpdated
A Study of PRT3789 in Combination With Pembrolizumab in Patients With Advanced or Metastatic Solid Tumors With a SMARCA4 Mutation
PRT3789, pembrolizumab - Advanced Solid Tumor, Esophageal Cancer
Phase 2TerminatedPrelude Therapeutics Incorporated62025-06-032026-02-02
PRT3789 Monotherapy and in Combo w/Docetaxel in Participants w/Advanced or Metastatic Solid Tumors w/SMARCA4 Mutation
PRT3789, Docetaxel - Advanced Solid Tumor, Metastatic Solid Tumor
Phase 1CompletedPrelude Therapeutics Incorporated1352023-05-022025-10-16
Online Study of People Who Have Genetic Changes and Features of Autism: Simons Searchlight
16P11.2 Deletion Syndrome, 16p11.2 Duplications
RecruitingSimons Searchlight1000002010-10-012026-07-23

Narrower conditions

Neoplasm Metastasis (2)  ·  15q24 Microdeletion (1)  ·  16p11.2 Deletion Syndrome (1)  ·  Chromosome 15q13.3 Microdeletion Syndrome (1)  ·  Chromosome 17q21.31 Deletion Syndrome (1)  ·  Chromosome 1q21.1 Deletion Syndrome, 1.35-Mb (1)  ·  Chromosome 1q21.1 Duplication Syndrome (1)  ·  Chromosome 2q37 deletion syndrome (1)  ·  Cornea Plana 1 (1)  ·  Cri-du-Chat Syndrome (1)  ·  Epileptic Encephalopathy, Early Infantile, 4 (1)  ·  Esophageal Neoplasms (1)  ·  Hereditary Sensory and Autonomic Neuropathies (1)  ·  Rhabdoid Tumor Predisposition Syndrome 2 (1)

Broader conditions

Neoplasms (2)  ·  Neoplastic Processes (2)  ·  Pathologic Processes (2)  ·  Pathological Conditions, Signs and Symptoms (2)  ·  Abnormalities, Multiple (1)  ·  Chromosome Disorders (1)  ·  Congenital Abnormalities (1)  ·  Congenital, Hereditary, and Neonatal Diseases and Abnormalities (1)  ·  Digestive System Diseases (1)  ·  Digestive System Neoplasms (1)  ·  Esophageal Diseases (1)  ·  Gastrointestinal Diseases (1)  ·  Gastrointestinal Neoplasms (1)  ·  Genetic Diseases, Inborn (1)  ·  Head and Neck Neoplasms (1)

Interventions

Docetaxel (1)  ·  pembrolizumab (1)

Sponsors

Prelude Therapeutics Incorporated (2)  ·  Simons Searchlight (1)

Countries

United States (3)  ·  Spain (2)  ·  France (1)  ·  Netherlands (1)  ·  Singapore (1)

Top investigators

Cora Taylor, PhD (1)  ·  Wendy Chung, MD PhD (1)