30
Participants
Start Date
August 31, 2011
Primary Completion Date
December 31, 2011
Study Completion Date
December 31, 2011
Teriparatide
Administered subcutaneously during the Treatment Period
Aspara-CA 600 mg
Administered orally throughout the study
Alfarol 1.0 µg
Administered orally throughout the study
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Tokyo
Eli Lilly and Company
INDUSTRY