A Multiple Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Romosozumab (AMG 785)

PHASE1CompletedINTERVENTIONAL
Enrollment

48

Participants

Timeline

Start Date

November 14, 2007

Primary Completion Date

December 2, 2008

Study Completion Date

December 2, 2008

Conditions
PostmenopausalOsteopenia
Interventions
DRUG

Romosozumab

Administered by subcutaneous injection

DRUG

Placebo

Administered by subcutaneous injection

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Amgen

INDUSTRY