Study of Nivolumab and Relatlimab in Advanced Mismatch Repair Deficient Cancers Resistant to Prior PD-(L)1 Inhibitor

Part of paid clinical trials in Los Angeles, California.

Sponsor
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Study ID
NCT03607890
Phase
PHASE2
Status
Active Not Recruiting

Conditions

  • MSI-H Tumors
  • Refractory MSI - H Solid Tumors Prior of PD-(L) 1 Therapy

Eligibility Criteria

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

Interventions

  • Nivolumab — DRUG
    Patients will receive treatment every 28 days for up to 2 years. Nivolumab will be administered IV on day 1 (28 day cycle).
  • Relatlimab — DRUG
    Patients will receive treatment every 28 days up to 2 years. Relatlimab will be administered IV on day 1 (28 day cycle).
  • Nivolumab — DRUG
    Patients will receive treatment every 28 days for up to 2 years. Nivolumab will be administered IV on day 1 (28 day cycle).
  • Relatlimab — DRUG
    Patients will receive treatment every 28 days up to 2 years. Relatlimab will be administered IV on day 1 (28 day cycle).
  • Nivolumab — DRUG
    Patients will receive treatment every 28 days for up to 2 years. Nivolumab will be administered IV on day 1 (28 day cycle).
  • Relatlimab — DRUG
    Patients will receive treatment every 28 days up to 2 years. Relatlimab will be administered IV on day 1 (28 day cycle).

Study Details

The purpose of this study is to evaluate the safety and clinical activity of nivolumab and relatlimab in patients with microsatellite instability high (MSI-H) solid tumors refractory to prior PD-(L)1 therapy.

Key Dates

Start date
Nov 16, 2018
Status verified
Mar 2026
Primary completion
Oct 31, 2026
Completion
Oct 31, 2026

Study Design

Enrollment
38 participants (actual)
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Cohort 1: Nivolumab and Relatlimab
    480mg/160mg (co-administered)
  • Experimental: Cohort 2: Nivolumab and Relatlimab
    480mg/960mg or 480mg/160mg (sequential administration)
  • Experimental: Cohort 3: Nivolumab and Relatlimab
    480mg/480mg (sequential administration)

Primary Outcome Measure

Objective response rate (ORR) using Response Evaluation Criteria in Solid Tumors (RECIST 1.1) [ Time Frame: 4 years ]

Locations (2)

FacilityCityStateZIPSite coordinators
Cedars Sinai Medical CenterLos AngelesCalifornia90048-
Sidney Kimmel Comprehensive Cancer CenterBaltimoreMaryland21231-

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