A Study of Cobimetinib Plus Atezolizumab Versus Pembrolizumab in Participants With Previously Untreated Advanced BRAFv600 Wild-Type Melanoma

Part of paid clinical trials in Tucson, Arizona.

Sponsor
Hoffmann-La Roche
Study ID
NCT03273153
Phase
PHASE3
Status
Terminated

Conditions

  • Advanced BRAFV600 Wild-type Melanoma

Eligibility Criteria

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

Interventions

  • Cobimetinib — DRUG
    Cobimetinib 60 mg tablets orally once daily on a 21 days on, 7 days off schedule.
  • Atezolizumab — DRUG
    Atezolizumab 840 mg as IV infusion once in every 2 weeks.
  • Pembrolizumab — DRUG
    Pembrolizumab 200 mg as IV infusion once in every 3 weeks.

Study Details

This is a Phase III, multicenter, open-label, randomized study designed to evaluate the efficacy, safety, and pharmacokinetics of cobimetinib plus atezolizumab compared with pembrolizumab in treatment-naive participants with advanced BRAFV600 wild-type melanoma.

Key Dates

Start date
Dec 11, 2017
Status verified
Aug 2022
Primary completion
Apr 15, 2019
Completion
Feb 19, 2021

Study Design

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

Arms

  • Experimental: Cobimetinib and Atezolizumab
    Participants will receive 60 mg of cobimetinib orally from Days 1 to 21 along with 840 mg of atezolizumab by intravenous (IV) infusion on Days 1 and 15 of each 28-day cycle until investigator-determined disease progression, unacceptable toxicity, death, patient or physician decision to withdraw, or pregnancy, whichever occurs first. There will be no cobimetinib administration for 7 days (Days 22-28) in each cycle.
  • Active Comparator: Pembrolizumab
    Participants will receive 200 mg of pembrolizumab administered by IV infusion every 3 weeks (Q3W) until investigator-determined disease progression, unacceptable toxicity, death, patient or physician decision to withdraw, or pregnancy, whichever occurs first.

Primary Outcome Measure

Progression Free Survival (PFS) as Determined by the Independent Review Committee (IRC) [ Time Frame: Every 8 weeks (wks) from Day (D) 1 of Cycle (C) 1 through approximately 16 months ]

Locations (23)

FacilityCityStateZIPSite coordinators
University of Arizona Cancer CenterTucsonArizona85719-
City of Hope Comprehensive Cancer CenterDuarteCalifornia91010-
USC Norris Cancer CenterLos AngelesCalifornia90033-
USC Norris Cancer Center; USC Oncology Hematology Newport BeachNewport BeachCalifornia92663-
University of California at Irvine Medical Center; Department of OncologyOrangeCalifornia92868-
Stanford Comprehensive Cancer CenterStanfordCalifornia94305-
UF Health Cancer Center at Orlando HealthOrlandoFlorida32824-
Florida Cancer Specialist, North RegionSt. PetersburgFlorida33705-
Moffitt Cancer CenterTampaFlorida33612-
Florida Cancer SpecialistsWest Palm BeachFlorida33401-
Northwestern UniversityChicagoIllinois60611-
Massachusetts General Hospital;Hematology/ OncologyBostonMassachusetts02114-
University of Michigan; Michigan Institute for Clinical and Health Research (MICHR)Ann ArborMichigan48109-
Dartmouth-Hitchcock Medical Center; Hematology/OncologyLebanonNew Hampshire03756-
Morristown Medical CenterMorristownNew Jersey07962-
Forsythe Memorial Hospital Inc., dba Novant Health Oncology SpecialistsWinston-SalemNorth Carolina27103-
TriHealth Hatton Institute; Surgical EducationCincinnatiOhio45220-
St. Luke's University Health networkBethlehemPennsylvania18015-
Thomas Jefferson University Hospital;Medical OncologyPhiladelphiaPennsylvania19107-
SCRI Tennessee Oncology ChattanoogaChattanoogaTennessee37404-
Sarah Cannon Research InstituteNashvilleTennessee37203-
M.D Anderson Cancer Center; Uni of Texas At HoustonHoustonTexas77030-
West Virginia University Hospitals IncMorgantownWest Virginia26056-

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