A Study of Combination Nivolumab and Ipilimumab Retreatment in Patients With Advanced Renal Cell Carcinoma

Part of paid clinical trials in St Louis, Missouri.

Sponsor
Bristol-Myers Squibb
Study ID
NCT04088500
Phase
PHASE2
Status
Terminated

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Nivolumab — BIOLOGICAL
    Specific dose on specific days
  • Ipilimumab — BIOLOGICAL
    Specific dose on specific days

Study Details

The purpose of the study is to assess the effectiveness of re-induction with Nivolumab combined with ipilimumab.

Key Dates

Start date
Sep 3, 2020
Status verified
Dec 2022
Primary completion
Nov 15, 2021
Completion
Nov 15, 2021

Study Design

Enrollment
5 participants (actual)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: Nivolumab + Ipilimumab (combination)
    Nivolumab + Ipilimumab (combination) Q3W for 4 doses

Primary Outcome Measure

Disease Control Rate (DCR) [ Time Frame: From first dose up to approximately 14 months ]

Locations (1)

FacilityCityStateZIPSite coordinators
Washington University School of Medicine in St. Louis WUSTLSt LouisMissouri63108-

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