Denosumab Adherence Preference Satisfaction Study

PHASE3CompletedINTERVENTIONAL
Enrollment

250

Participants

Timeline

Start Date

September 1, 2007

Primary Completion Date

June 1, 2009

Study Completion Date

June 1, 2010

Conditions
Osteoporosis
Interventions
DRUG

alendronate

Subjects will take 70 mg QW of oral alendronate for 1 year. If a subject is randomized to Treatment Sequence A they will receive alendronate for 1 year in Treatment Period 2. If a subject is randomized to Treatment Sequence B they will receive alendronate for 1 year in Treatment Period 1.

DRUG

denosumab

Subjects will receive 60 mg of denosumab Q6M SC for 1 year. If a subject is randomized to Treatment Sequence A they will receive denosumab for 1 year in Treatment Period 2. If a subject is randomized to Treatment Sequence B they will receive denosumab for 1 year in Treatment Period 1.

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Amgen

INDUSTRY

NCT00518531 - Denosumab Adherence Preference Satisfaction Study | Biotech Hunter | Biotech Hunter