A Study of an Anti-KIR Antibody Lirilumab in Combination With an Anti-PD1 Antibody Nivolumab and Nivolumab Plus an Anti-CTLA-4 Ipilimumab Antibody in Patients With Advanced Solid Tumors

Part of paid clinical trials in San Francisco, California.

Sponsor
Bristol-Myers Squibb
Study ID
NCT01714739
Phase
PHASE1/PHASE2
Status
Completed

Conditions

  • CANCER,NOS

Eligibility Criteria

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

Interventions

  • Lirilumab — DRUG
    Specified dose on specified days.
  • Nivolumab — DRUG
    Specified dose on specified days.
  • Ipilimumab — DRUG
    Specified dose on specified days.

Study Details

To assess the safety and tolerability and preliminary anti-tumor activity of lirilumab (BMS-986015) given in combination with nivolumab (BMS-936558) and to identify dose limiting toxicities (DLTs) and the maximally tolerated dose (MTD) of the combination. In addition, to assess the combinations of lirilumab and nivolumab or lirilumab and nivolumab plus ipilimumab (BMS-734016) in subjects with advanced (metastatic and/or unresectable) refractory solid tumors.

Key Dates

Start date
Oct 7, 2012
Status verified
Jan 2023
Primary completion
Dec 13, 2019
Completion
Dec 13, 2019

Study Design

Enrollment
337 participants (actual)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Part 1
    Dose Escalation and Initial Signal Detection in Multiple Solid Tumors - Nivolumab with Lirilumab
  • Experimental: Part 2 and 3: Cohort Expansion
    In platinum-refractory recurrent or metastatic SCCHN - Nivolumab with or without Lirilumab
  • Experimental: Part 4: Cohort Expansion
    Additional Signal Detection in Solid Tumors - Nivolumab with Lirilumab (Study Part 4 Removed; No Subjects Enrolled)
  • Experimental: Part 5 and 6
    Safety Lead-In and Additional Signal Detection in Solid Tumors -- Nivolumab Plus Ipilimumab with Lirilumab (Study Part 6 Removed; No Subjects Enrolled)

Primary Outcome Measure

Number of Participants With Adverse Events (AEs) - Parts 1, 2 and 5 [ Time Frame: From first dose to 150 days post last dose (up to an average of 51 weeks and a maximum of 2.5 years) ]

Locations (16)

FacilityCityStateZIPSite coordinators
UcsfSan FranciscoCalifornia94115-
Florida Cancer Affiliates - OcalaOcalaFlorida34471-
University Of Chicago Medical CenterChicagoIllinois60637-
Sidney Kimmel Comprehensive Cancer Center At Johns HopkinsLuthervilleMaryland21093-
Beth Israel Deaconess Med CtrBostonMassachusetts02215-
Dana Farber Cancer InstituteBostonMassachusetts02215-
Massachusetts General HospitalBostonMassachusetts02215-
Memorial Sloan Kettering Cancer CenterNew YorkNew York10065-
The Ohio State University Wexner Medical CenterColumbusOhio43210-
Providence Portland Med CtrPortlandOregon97213-
Thomas Jefferson University HospitalPhiladelphiaPennsylvania19107-
UPMC Eye and Ear InstitutePittsburghPennsylvania15213-
West Cancer CenterGermantownTennessee38138-
Texas Oncology-Central Austin Cancer CenterAustinTexas78731-
University Of Texas Medical Branch Of GalvestonGalvestonTexas77555-
University Of WashingtonSeattleWashington98195-

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