6
Participants
Start Date
January 31, 2014
Primary Completion Date
August 31, 2015
Study Completion Date
December 31, 2015
pegvisomant
Pegvisomant 20 mg subcutaneously Qday will be administered by the study subject for 28 days during this study.
San Francisco General Hospital, San Francisco
San Francisco General Hospital
OTHER
University of California, San Francisco
OTHER