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Safety Study of Enoblituzumab (MGA271) in Combination With Ipilimumab in Refractory Cancer

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Contents

clinicaltrials.gov/study/NCT02381314
Is a
‌
Clinical study
0

Clinical Study attributes

NCT Number
NCT023813140
Health Conditions in Trial
Melanoma
Melanoma
0
Trial Recruitment Size
240
Trial Sponsor
MacroGenics
MacroGenics
0
Clinical Trial Start Date
March 26, 2015
0
Primary Completion Date
November 9, 2017
0
Study Completion Date
September 26, 2018
0
Clinical Trial Study Type
Interventional0
Interventional Trial Purpose
Treatment0
Intervention Type
Biological0
Intervention Name
enoblituzumab plus ipilimumab0
Interventional Trial Phase
Phase 10
Participating Facility
Columbia University Medical Center
Columbia University Medical Center
0
University of Wisconsin
University of Wisconsin
0
‌
Mount Sinai Medical Center
0
Providence Portland Medical Center
Providence Portland Medical Center
0
University of Chicago
University of Chicago
0
Yale University
Yale University
0
Official Name
A Phase 1, Open-Label, Dose Escalation Study of MGA271 in Combination With Ipilimumab in Patients With Melanoma, Non-Small Cell Lung Cancer, and Other Cancers0
Last Updated
February 8, 2022
0
Allocation Type
NA0
Intervention Model
Single Group Assignment0
Masking Type
None (Open Label)0
Study summary

The purpose of this study is to evaluate the safety of enoblituzumab (MGA271) in combination with Yervoy (ipilimumab) when given to patients with B7-H3-expressing melanoma, squamous cell carcinoma of the head and neck (SCCHN), non small cell lung cancer (NSCLC) and other B7-H3 expressing cancers. The study will also evaluate what is the best dose of enoblituzumab to use when given with ipilimumab. Assessments will also be done to see how the drug acts in the body (pharmacokinetics (PK), pharmacodynamics) and to evaluate potential anti-tumor activity of enoblituzumab in combination with ipilimumab.

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