Safety Study of Enoblituzumab (MGA271) in Combination With Pembrolizumab or MGA012 in Refractory Cancer

PHASE1CompletedINTERVENTIONAL
Enrollment

146

Participants

Timeline

Start Date

July 31, 2015

Primary Completion Date

August 18, 2021

Study Completion Date

August 18, 2021

Conditions
MelanomaHead and Neck CancerNon Small Cell Lung CancerUrothelial Carcinoma
Interventions
BIOLOGICAL

Enoblituzumab Schedule 1

enoblituzumab is administered by IV infusion once per week for up to 51 doses.

BIOLOGICAL

Pembrolizumab

Pembrolizumab is administered by IV infusion every 3 weeks for up to 17 doses.

BIOLOGICAL

Enoblituzumab Schedule 2

Enoblituzumab is administered by IV infusion every 3 weeks for up to 17 doses

BIOLOGICAL

retifanlimab

Retifanlimab is administered by IV infusion every 3 weeks for up to 17 doses

Trial Locations (20)

10032

Columbia University Medical Center, New York

14263

Roswell Park Cancer Institute, Buffalo

15232

University of Pittsburg, Pittsburgh

19104

Hospital of the University of Pennsylvania/Abramson Cancer Center, Philadelphia

19713

Christiana Care Health Services, Inc., Newark

21201

University of Maryland Greenbaum Cancer Center, Baltimore

29605

Greenville Health System, Greenville

32224

Mayo Clinic - FL, Jacksonville

33612

Moffitt Cancer Center, Tampa

40202

Norton Cancer Institute Research Program, Louisville

44718

Gabrail Cancer Institute, Canton

49503

South Texas Accelerated Research Therapeutics, LLC - Midwest, Grand Rapids

55905

Mayo Clinic - MN, Rochester

68130

Nebraska Cancer Specialists, Omaha

75230

Mary Crowley Cancer Research Center, Dallas

78229

South Texas Accelerated Research Therapeutics, LLC, San Antonio

85259

Mayo Clinic - AZ, Scottsdale

89169

Comprehensive Cancer Centers of Nevada, Las Vegas

02215

Dana-Farber Cancer Institute, Boston

02903

Rhode Island Hospital, Providence

Sponsors

Lead Sponsor

All Listed Sponsors
lead

MacroGenics

INDUSTRY