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Safety Study of MGAH22 in HER2-positive Carcinomas

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Contents

clinicaltrials.gov/study/NCT01148849
Is a
‌
Clinical study
0

Clinical Study attributes

NCT Number
NCT011488490
Health Conditions in Trial
‌
Breast Cancer
0
Trial Recruitment Size
660
Trial Sponsor
MacroGenics
MacroGenics
0
Trial Collaborator
0
Clinical Trial Start Date
2010
0
Primary Completion Date
June 14, 2022
0
Study Completion Date
June 14, 2022
0
Clinical Trial Study Type
Interventional0
Interventional Trial Purpose
Treatment0
Intervention Type
Biological0
Intervention Name
margetuximab0
Interventional Trial Phase
Phase 10
Participating Facility
Seoul National University Hospital
Seoul National University Hospital
0
National Cancer Institute
National Cancer Institute
0
Sarah Cannon Research Institute
Sarah Cannon Research Institute
0
Official Name
A Phase 1, Dose Escalation Study of MGAH22 in Patients With Refractory HER2 Positive Breast Cancer and Patients With Other HER2 Positive Carcinomas for Whom No Standard Therapy Is Available0
Last Updated
October 19, 2022
0
Allocation Type
Non-Randomized0
Intervention Model
Single Group Assignment0
Masking Type
None (Open Label)0
Study summary

The purpose of this study is to determine if MGAH22 is safe when given by intravenous (IV) infusion to patients with HER2-positive cancer. The study will also evaluate how long MGAH22 stays in the blood and how long it takes for it to leave the body, what is the highest dose that can safely be given, and whether it has an effect on tumors.

Timeline

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