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Spots Global Cancer Trial Database for Highly Selective CDK7 Inhibitor Q901 in Selected Advanced Solid Tumors

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Trial Identification

Brief Title: Highly Selective CDK7 Inhibitor Q901 in Selected Advanced Solid Tumors

Official Title: A Phase 1/2 Multicenter, Open-label, Dose-escalation, Safety, Pharmacodynamic, and Pharmacokinetic Study of Q901Administered Via Intravenous Infusion as Monotherapy and in Combination With Pembrolizumab in Adult Patients With Selected Advanced Solid Tumors With Cohort Expansions at the Recommended Phase 2 Dose

Study ID: NCT05394103

Study Description

Brief Summary: Multicenter, open-label, dose-escalation, safety, tolerability, PK and pharmacodynamic study with a dose expansion at the RP2D to evaluate safety and potential antitumor activity of Q901 as a monotherapy and in combination with pembrolizumab

Detailed Description:

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Mayo Clinic, Phoenix, Arizona, United States

University of Southern California, Los Angeles, California, United States

Mayo Clinic, Jacksonville, Florida, United States

Northwestern University, Chicago, Illinois, United States

Mayo Clinic, Rochester, Minnesota, United States

Atlantic Health System Hospital, Morristown, New Jersey, United States

Mary Crowley Cancer Research, Dallas, Texas, United States

Asan Medical Center, Seoul, , Korea, Republic of

Severance Hospital, Seoul, , Korea, Republic of

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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