drugset / Trial / NCT05406713

Pembrolizumab in Muscle-invasive Bladder Cancer

NCT05406713 ↗

Phase 2 Active not recruiting 46 enrolled Matthew Galsky Merck Sharp & Dohme LLC · collab
NaSingle-groupOpen-labelTreatment

Summary

Subjects with cT2-T3N0M0 urothelial cancer of the bladder will be enrolled. After completing two cycles of pembrolizumab, subjects will undergo a restaging MRI of the abdomen and pelvis with a standard acquisition protocol (as outlined in the protocol) as well as CT chest. A CT of the abdomen and pelvis may be performed if there are contraindications to MRI. Patients will also undergo a restaging cystoscopy and biopsies/TURBT as outlined in the protocol. Patients achieving a clinical complete response to treatment (defined in the protocol) will proceed with "maintenance" single agent pembrolizumab followed by surveillance. All other patients will proceed with standard of care local therapy as per their treating physicians followed by "adjuvant" pembrolizumab.

Timeline

Start
2022-07-13
Primary completion
2027-01-31
Completion
2028-01-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Pembrolizumab Monoclonal antibody 400 mg Intravenous