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Monoclonal Antibodies

Pembrolizumab and Ramucirumab for Bladder Cancer

Phase 2
Waitlist Available
Led By Michael Hurwitz, PhD, MD
Research Sponsored by Yale University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 24 months
Awards & highlights
No Placebo-Only Group

Summary

This trial will study how well a combination of pembrolizumab and ramucirumab works in treating patients with TCC that has progressed after treatment with checkpoint inhibitors.

Eligible Conditions
  • Bladder Cancer

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 24 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 24 months for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Overall response rate (ORR)
Secondary study objectives
Overall survival (OS)
Progression free survival (PFS)

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: Pembrolizumab and RamucirumabExperimental Treatment1 Intervention
Patients with progressive transitional cell carcinoma after treatment with an immune checkpoint inhibitor will receive Pembrolizumab and Ramucirumab.

Find a Location

Who is running the clinical trial?

Yale UniversityLead Sponsor
1,924 Previous Clinical Trials
3,031,658 Total Patients Enrolled
Michael Hurwitz, PhD, MD5.01 ReviewsPrincipal Investigator - Assistant Professor of Medicine (Medical Oncology) Yale University
Yale University
5Patient Review
Dr. Hurwitz is an amazing oncologist who is both kind and brilliant. He talks to patients in a way that is easy to understand, and he is very patient. He is also very funny and professional.
~0 spots leftby Nov 2025