Urothelial Cancer Clinical Trials

Find Urothelial Cancer Clinical Trials Near You

Pembrolizumab Maintenance After Enfortumab Vedotin/Pembrolizumab Induction in Front-Line Metastatic Urothelial Carcinoma

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This is a single-arm, open-label, non-randomized Phase II trial evaluating the efficacy of induction therapy with enfortumab vedotin (EV) plus pembrolizumab (P) for 18 weeks (6 cycles), followed by maintenance pembrolizumab in treatment-naïve patients with metastatic urothelial carcinoma (mUC). Approximately 97 patients will be enrolled. Induction consists of EV (1.25 mg/kg IV on Days 1 and 8 of each 21-day cycle; starting dose of 1 mg/kg allowed) and P (200 mg IV on Day 1 of each cycle). Radiographic assessments occur after 3 and 6 cycles. Patients achieving complete or partial response transition to maintenance P (400 mg IV every 6 weeks or 200 mg IV every 3 weeks) for up to 2 years. Dose modifications for EV are permitted per protocol; no dose adjustments for P. Treatment continues until disease progression, unacceptable toxicity, or completion of maintenance therapy. Patients will enter long-term or survival follow-up as applicable.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients must have histologically and radiographically confirmed locally advanced, unresectable urothelial carcinoma.

• Patients should not have received prior systemic therapy for metastatic disease.

• Patients must have measurable disease, defined as at least one lesion that can be accurately measured in at least one dimension in accordance with RECIST criteria v1.1

• Patients may have received prior neoadjuvant or adjuvant immune checkpoint inhibitor therapy for localized disease and are eligible if they completed the treatment ≥12 months prior to initiating treatment on this clinical trial.

• ECOG performance status 0-2

• Ability to understand and willingness to sign a written informed consent and HIPAA consent document

• Archival tumor biospecimen (when available) must be procured for correlative evaluation. If tumor tissue is not available or accessible despite good faith efforts, patient may still be treated on study. Formalin fixed, paraffin embedded (FFPE) tissue block(s) or at least 25 unbaked, unstained slides are required. Tissue samples taken from a metastatic lesion prior to the start of screening are acceptable.

• Normal organ and marrow function as defined below.

‣ Absolute neutrophil count \> 1,000/mm3 unless patient has constitutional neutropenia

⁃ Platelets \> 100,000/µl

⁃ Hemoglobin \> 8.0 g/dL

⁃ Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) \<2.5 x upper limit of normal (ULN) or \<3.5 x ULN if liver metastases

⁃ Creatinine Clearance \>20 ml/min

Locations
United States
Pennsylvania
Fox Chase Cancer Center - Philadelphia
RECRUITING
Philadelphia
Contact Information
Primary
Ryan Romasko, MBA
ryan.romasko@fccc.edu
215-214-1515
Time Frame
Start Date: 2026-01-23
Estimated Completion Date: 2029-09-03
Participants
Target number of participants: 97
Treatments
Experimental: Induction EV + Pembrolizumab Followed by Maintenance Pembrolizumab
Participants will receive induction therapy with enfortumab vedotin (EV) plus pembrolizumab (P) for 6 cycles (approximately 18 weeks). EV will be administered at 1.25 mg/kg IV on Days 1 and 8 of each 21-day cycle (starting dose of 1 mg/kg allowed), and pembrolizumab at 200 mg IV on Day 1 of each cycle. Patients achieving complete or partial response will transition to maintenance pembrolizumab at 400 mg IV every 6 weeks or 200 mg IV every 3 weeks for up to 2 years. Dose modifications for EV are permitted per protocol; no dose adjustments for pembrolizumab. Treatment continues until disease progression, unacceptable toxicity, or completion of maintenance therapy.
Related Therapeutic Areas
Sponsors
Collaborators: United States Department of Defense
Leads: Fox Chase Cancer Center

This content was sourced from clinicaltrials.gov

Similar Clinical Trials