Skip to content
Study details
Enrolling now

Gemcitabine and Carboplatin After Progression on Enfortumab Vedotin and Pembrolizumab in Advanced/Metastatic Urothelial Carcinoma

Fox Chase Cancer Center
NCT IDNCT07043972ClinicalTrials.gov data as of Apr 2026
Phase

Phase 2

Target enrollment

55

Study length

about 5.5 years

Ages

18+

Locations

2 sites in PA

What this study is about

Researchers are testing if a chemotherapy combination called gemcitabine and carboplatin (GC) works to treat advanced urothelial cancer in people who have already been treated with enfortumab vedotin and pembrolizumab (EVP). The trial will also learn about the efficacy and safety of GC in these patients. Researchers will trial how GC affects survival, cancer control, and quality of life.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take Carboplatin
  • 2.Take Gemcitabine

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Injection / IV

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

carboplatin, gemcitabine

Drug routes

injection (Injection)

Endpoints

Primary: Best overall response (Complete response (CR), partial response (PR), stable disease (SD), progressive disease (PD) to gemcitabine plus carboplatin defined per RECIST v 1.1

Secondary: To evaluate overall survival (OS) as a function of time since study enrollment in patients receiving GC after prior exposure to EVP, To evaluate progression free survival (PFS) as a function of time since study enrollment in patients receiving GC after prior exposure to EVP, To evaluate the disease control rate (DCR) of gemcitabine plus carboplatin after prior exposure to EVP