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RECRUITING
NCT07484022
PHASE1

Study of GB-4362 With Enfortumab Vedotin and Pembrolizumab for Advanced Urothelial Cancer

Sponsor: Generate Biomedicines

View on ClinicalTrials.gov

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

DRUG

GB-4362

GB-4362 is an investigational monoclonal antibody

DRUG

enfortumab vedotin (EV)

Enfortumab vedotin is an antibody-drug conjugate targeting Nectin-4 that delivers the cytotoxic payload monomethyl auristatin E (MMAE).

DRUG

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