Clinical Trials · NCT01801397

A Pilot Study to Evaluate the Effect of Forsteo (Teriparatide, 1-34-rh-PTH) in Anorexia Nervosa Patients With Low Bone Mineral Density and Increased Bone Fagility (FAN-Trial)

Phase
Phase 3
Recruitment status
Unknown
Sponsor
University of Zurich
Enrollment
10
Start date
Mar 2014
Locations
2 sites, Switzerland
Primary endpoint
To assess the efficacy of Teriparatide (Forsteo®) in increasing the bone mineral density in the lumbar spine, total hip and femoral neck in patients with anorexia nervosa and low bone density at months 12 and 24.
View Teriparatide compound reference