Summary

Eligibility
for people ages 18 years and up (full criteria)
Location
at UCSF
Dates
study started
study ends around

Description

Summary

Researchers are looking for new ways to treat people with urothelial cancer (UC) that is locally advanced or metastatic. The standard treatment for locally advanced or metastatic UC is enfortumab vedotin (EV) given with pembrolizumab.

The goals of this study are to learn about:

  • The safety of the study treatment when given with standard treatment and if people tolerate it
  • The number of people who have the cancer respond (cancer gets smaller or goes away) with the new study treatment when given with standard treatment.

Official Title

A Phase 1/2 Open-Label Rolling-Arm Umbrella Platform Study of Investigational Agents in Combination With Enfortumab Vedotin Plus Pembrolizumab as First-Line Treatment in Participants With Locally Advanced or Metastatic Urothelial Carcinoma: KEYMAKER-U04-Substudy 04D

Details

This is a substudy of the master protocol MK-3475-U04 (KEYMAKER-U04)

Keywords

Bladder Cancer, Urinary Bladder Neoplasms, enfortumab vedotin, pembrolizumab, Rescue Medication, MK-3120 + Enfortumab Vedotin (EV) + Pembrolizumab

Eligibility

You can join if…

Open to people ages 18 years and up

The main inclusion criteria include but are not limited to the following:

  • Has histologically documented urothelial carcinoma (UC) that is locally advanced and unresectable or metastatic
  • Must provide a newly obtained or archival tumor tissue sample (core or excisional biopsy)
  • Must not have received prior systemic therapy for locally advanced or metastatic UC
  • If infected with Human Immunodeficiency Virus (HIV), has well controlled HIV on antiretroviral therapy
  • If positive for hepatitis B surface antigen, has received hepatitis B virus (HBV) antiviral therapy for at least 4 weeks and has undetectable HBV viral load before randomization
  • If participant has a history of hepatitis C virus (HCV), has undetectable HCV viral load before randomization

You CAN'T join if...

The main exclusion criteria include but are not limited to the following:

  • Has history of documented severe dry eye syndrome, severe Meibomian gland disease and/or blepharitis, or corneal disease that prevents/delays corneal healing
  • Has active keratitis or corneal ulcerations
  • Has active inflammatory bowel disease requiring immunosuppressive medication, or previous history of inflammatory bowel disease (eg, Crohn's disease, ulcerative colitis, or chronic diarrhea)
  • Has uncontrolled, significant cardiovascular disease or cerebrovascular disease within the 6 months preceding study intervention
  • Has a history of uncontrolled diabetes
  • Has pleural effusion, ascites, and/or pericardial effusion that are symptomatic or require repeated drainage
  • Has active autoimmune disease that has required systemic treatment in the past 2 years
  • Has known additional malignancy that is progressing or has required active treatment within the past 2 years
  • Has known active central nervous system metastases and/or carcinomatous meningitis
  • Has a history of (noninfectious) pneumonitis/interstitial lung disease that required steroids, or has current pneumonitis/interstitial lung disease
  • Has an active infection requiring systemic therapy
  • If infected with HIV, has a history of Kaposi's sarcoma and/or Multicentric Castleman's Disease
  • Has concurrent active HBV and HCV infection
  • Has a history of stem cell/solid organ transplant

Locations

  • UCSF Medical Center at Mission Bay ( Site 5044) accepting new patients
    San Francisco California 94158 United States
  • Huntsman Cancer Institute ( Site 5041) accepting new patients
    Salt Lake City Utah 84112-5550 United States

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Merck Sharp & Dohme LLC
Links
Plain Language Summary
ID
NCT07232602
Phase
Phase 1/2 research study
Study Type
Interventional
Participants
Expecting 55 study participants
Last Updated