A Study of Emibetuzumab in Non Small Cell Lung Cancer (NSCLC) Participants

Part of paid clinical trials in Birmingham, Alabama.

Sponsor
Eli Lilly and Company
Study ID
NCT01900652
Phase
PHASE2
Status
Completed

Conditions

  • Carcinoma, Non-Small-Cell Lung

Eligibility Criteria

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

Interventions

  • Emibetuzumab — DRUG
    Administered IV
  • Erlotinib — DRUG
    Administered Orally

Study Details

The primary purpose of this study is to evaluate the efficacy of the study drug known as LY2875358, administered alone or in combination with a second drug named Erlotinib, in participants affected by a defined type of lung cancer (MET biomarker diagnostic positive Non-Small-Cell Lung Cancer) that experienced a disease progression during the most recent treatment with Erlotinib.

Key Dates

First listed
Jul 16, 2013
Start date
Aug 31, 2013
Status verified
Sep 2019
Primary completion
Feb 28, 2015
Completion
Mar 31, 2016

Study Design

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

Arms

  • Experimental: Arm A: Emibetuzumab plus Erlotinib
    750 milligram (mg) Emibetuzumab flat dose given as a 1.5 hour intravenous (IV) infusion on Days 1 and 15 of a 28-day cycle and Erlotinib 150 mg given orally once daily on a 28-day cycle.
  • Experimental: Arm B: Emibetuzumab
    750 mg Emibetuzumab flat dose given as a 1.5-hour IV infusion on Days 1 and 15 of a 28-day cycle.

Primary Outcome Measure

Percentage of Participants Achieving Complete Response (CR) or Partial Response (PR) (Overall Response Rate [ORR]) [ Time Frame: Baseline to Objective Disease Progression or Start of New Anticancer Therapy (Up to 15 Months) ]

Locations (32)

FacilityCityStateZIPSite coordinators
University of Alabama at BirminghamBirminghamAlabama35294-
University of California - San DiegoLa JollaCalifornia92037-
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.Los AngelesCalifornia90048-
University of California, Davis - Health SystemsSacramentoCalifornia95817-
UCLASanta MonicaCalifornia90404-
University of Colorado Health Sciences CenterAuroraColorado80045-
Georgetown University Medical Center IRBWashington D.C.District of Columbia20007-
Florida Cancer SpecialistsFort MyersFlorida33916-2233-
Florida Cancer SpecialistsSt. PetersburgFlorida33705-
H Lee Moffitt Cancer CenterTampaFlorida33612-
Northeast Georgia Cancer Care, LLCAthensGeorgia30607-
Emory UniversityAtlantaGeorgia30322-
University of Iowa HospitalIowa CityIowa52242-
University of Kansas Medical CenterWestwoodKansas66205-
Massachusetts General HospitalBostonMassachusetts02114-
Karmanos Cancer InstituteDetroitMichigan48201-
Mayo ClinicRochesterMinnesota55905-
Washington University Medical CenterSt LouisMissouri63110-
Billings Clinic Research CenterBillingsMontana59101-
Dartmouth Hitchcock Medical CenterLebanonNew Hampshire03756-
Columbia UniversityNew YorkNew York10032-
Carolinas Medical CenterCharlotteNorth Carolina28204-
Oncology Hematology Care IncCincinnatiOhio45242-
Portland VA Medical CenterPortlandOregon97213-
Fox Chase Cancer CenterPhiladelphiaPennsylvania19111-
Tennessee Oncology PLLCChattanoogaTennessee37404-
The West ClinicMemphisTennessee38120-
Tennessee Oncology PLLCNashvilleTennessee37203-
MS Center at EvergreenKirklandWashington98034-
Group HealthSeattleWashington98112-
Seattle Cancer Care AllianceSeattleWashington98109-
Multicare Health SystemTacomaWashington98405-

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