42
Participants
Start Date
December 31, 2008
Primary Completion Date
December 31, 2011
Study Completion Date
May 31, 2013
Placebo
single dose IV or SC administration
KRN23
Single IV administration on day 1: 0.003, 0.01, 0.03, 0.1 and 0.3 mg/kg and Single SC administration on day 1: 0.1, 0.3, 0.6 and 1.0 mg/kg
Duke Clinical Research Unit, Durham
University of Texas Health Science Center at Houston, Houston
Yale University School of Medicine, New Haven
General Clinical Research Center, Indiana University School of Medicine, Indianapolis
Collaborators (1)
Kyowa Hakko Kirin Pharma, Inc.
INDUSTRY
Kyowa Kirin Co., Ltd.
INDUSTRY