Romosozumab/Denosumab Study for Premenopausal IOP

PHASE2Active, not recruitingINTERVENTIONAL
Enrollment

31

Participants

Timeline

Start Date

March 12, 2021

Primary Completion Date

March 31, 2026

Study Completion Date

March 31, 2027

Conditions
Premenopausal Idiopathic Osteoporosis
Interventions
DRUG

Romosozumab Prefilled Syringe [Evenity]

2 syringes of 105 MG/1.17 mL subcutaneous solution injected one after the other, once a month from study baseline through 11 month visit

DRUG

Denosumab 60 MG/ML Prefilled Syringe [Prolia]

1 subcutaneous injection of 60 mg/mL every six months from study 12 month visit through the 24 month visit. Injections occur at the 12 and 18 month visits.

Trial Locations (1)

10032

Columbia University Irving Medical Center, New York

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Amgen

INDUSTRY

lead

Columbia University

OTHER