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Study of GB-4362 With Enfortumab Vedotin and Pembrolizumab for Advanced Urothelial Cancer
Sponsor: Generate Biomedicines
Summary
The purpose of this study is to evaluate the safety and tolerability of an investigational drug called GB-4362 when it is given together with enfortumab vedotin and pembrolizumab in adults with advanced or metastatic urothelial cancer. GB-4362 is a monoclonal antibody designed to bind and neutralize free monomethyl auristatin E (MMAE), a chemotherapy payload released from enfortumab vedotin that is associated with side effects such as peripheral neuropathy.
Official title: A Phase 1, Open-Label Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of GB-4362 Administered With Enfortumab Vedotin and Pembrolizumab in Participants With Advanced Urothelial Cancer
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
37
Start Date
2026-04
Completion Date
2027-12
Last Updated
2026-05-15
Healthy Volunteers
No
Interventions
GB-4362
GB-4362 is an investigational monoclonal antibody
enfortumab vedotin (EV)
Enfortumab vedotin is an antibody-drug conjugate targeting Nectin-4 that delivers the cytotoxic payload monomethyl auristatin E (MMAE).
Pembrolizumab
Pembrolizumab is a programmed death-1 (PD-1) immune checkpoint inhibitor administered as standard-of-care therapy for advanced urothelial cancer.
Locations (6)
City of Hope
Duarte, California, United States
Orlando Health
Orlando, Florida, United States
Southeastern Regional Medical Center
Tucker, Georgia, United States
Midwestern Regional Medical Center
Zion, Illinois, United States
Start New York, LLC
Lake Success, New York, United States
MSK
New York, New York, United States