Last reviewed · How we verify

NCT05010590

Anabolic Therapy in Postmenopausal Osteoporosis

Active, enrolled Phase 4 Last updated 15 April 2026
What this trial tests

Phase 4 trial testing Romosozumab in Postmenopausal Osteoporosis in 50 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
24 March 2022
Primary endpoint
1 October 2027
1 November 2027

Quick facts

Lead sponsorMassachusetts General Hospital
PhasePhase 4
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment50
Start date24 March 2022
Primary completion1 October 2027
Estimated completion1 November 2027
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Massachusetts General Hospital

Who can join

45 and older, female only, with Postmenopausal Osteoporosis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

In this research study we want to learn more about the effect of two different FDA-approved medications in the treatment of osteoporosis.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. 3 months vs 12 months of romosozumab for postmenopausal osteoporosis (LIDA): an open-label, non-inferiority, randomised controlled trial.
    Leder BZ, Ramchand SK, Jordan M, Ryan S, et al · · 2026 · cited 2× · PMID 41621431 · DOI 10.1016/s2213-8587(25)00319-5

Verify or expand the search:

Other trials of Romosozumab

Trials testing the same drug.

Other recruiting trials for Postmenopausal Osteoporosis

Currently open trials in the same condition.

Other Massachusetts General Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05010590.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing