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Spots Global Cancer Trial Database for Study of Pembrolizumab and Ramucirumab in Pts With Progressive TCC After Treatment With an Immune Checkpoint Inhibitor

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Trial Identification

Brief Title: Study of Pembrolizumab and Ramucirumab in Pts With Progressive TCC After Treatment With an Immune Checkpoint Inhibitor

Official Title: A Phase II Trial of Pembrolizumab and Ramucirumab in Patients With Progressive Transitional Cell Carcinoma After Treatment With an Immune Checkpoint Inhibitor

Study ID: NCT04179110

Study Description

Brief Summary: This study is designed to evaluate response and survival of treatment with the combination of pembrolizumab and ramucirumab in patients with progressive metastatic TCC after immune checkpoint inhibitor treatment.

Detailed Description: This is a phase II, non-randomized single center study designed to evaluate response and survival of treatment with the combination of pembrolizumab and ramucirumab in patients with progressive metastatic TCC after immune checkpoint inhibitor treatment. The primary and secondary objectives are as follows: Primary: * Objective: To evaluate overall response rate (ORR) in patients treated with pembrolizumab and ramucirumab * Hypothesis: The ORR will be ≥15% greater than the historical rate in published literature of patients treated with pembrolizumab alone Secondary Objectives: * Objective: To evaluate progression free survival (PFS) in patients treated with pembrolizumab and ramucirumab * Hypothesis: The PFS will be ≥15% greater than the historical rate in published literature of patients treated with pembrolizumab alone * Objective: To evaluate overall survival (OS) in patients treated with pembrolizumab and ramucirumab * Hypothesis: The OS will be ≥15% greater than the historical rate in published literature of patients treated with pembrolizumab alone * Objective: To evaluate differences in ORR, PFS and OS in patients treated with pembrolizumab and ramucirumab stratified by Bellmunt criteria. * Hypothesis: Patients with high Bellmunt criteria scores will have lower rates of ORR, PFS and OS.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Yale University, New Haven, Connecticut, United States

Contact Details

Name: Michael Hurwitz, PhD, MD

Affiliation: Assistant Professor of Medicine (Medical Oncology) Yale University

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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