Teriparatide
FDA approved · RxParathyroid hormone analog
Also known as: Forteo, Bonsity, PTH 1-34, Teriparatida, Teriparatidum, 1-34-Human PTH, Human PTH (1-34), ZT-034, LY 333334, TERIPARATIDE RECOMBINANT HUMAN
Strong, human-grade evidence
- Regulatory standing. FDA-approved prescription medicine
- Human trials. Backed by controlled human studies
- Registered human trials. 182 registered studies on ClinicalTrials.gov, most advanced Phase 4
- 2 cited sources. Includes primary / regulatory sources
Computed with the same four public criteria as every profile. The human-evidence grade on an indexed profile is set automatically and may change when it is hand-reviewed. It is not a safety score, not a purity rating, and not medical advice, and not a claim that this compound treats, cures, or prevents any condition.
What it is
Teriparatide is a synthetic version of the first 34 amino acids of human parathyroid hormone, the active portion of the natural hormone. Given intermittently, it is thought to stimulate bone-forming cells more than bone-resorbing cells, which builds new bone rather than only slowing bone loss. It is sold under brand names including Forteo and Bonsity.
What the evidence shows
Teriparatide is FDA-approved for treating osteoporosis in people at high risk of fracture, including postmenopausal women, men, and people with glucocorticoid-induced osteoporosis. It is backed by a large body of human research, with 182 registered trials reaching Phase 4 and over 3,000 published papers, though uses outside its approved indications are less well established.
Key facts
Registered human trials
Live from ClinicalTrials.gov, refreshed daily.
Denosumab for Prevention of Post-Teriparatide Bone Loss in Premenopausal Women With IOP
µMRI of Therapeutic Intervention in Postmenopausal Osteoporosis
Effect of Teriparatide on Fracture Healing in Patients With Incomplete Atypical Femur Fractures
Clinical Results of Bisphosphonate and Denosumab Therapy Following Teriparatide Therapy for Japanese
Published literature
Live from Europe PMC. This is how much has been published, not how much is proven in humans.
Osteoporosis.
Clinical Practice. Postmenopausal Osteoporosis.
Atypical subtrochanteric and diaphyseal femoral fractures: second report of a task force of the American Society for Bone and Mineral Research.
Romosozumab in postmenopausal women with low bone mineral density.
Sources
- PubChem compound record (CID 16133850)
- FDA drug label on DailyMed
- Registered trials on ClinicalTrials.gov
- Published papers on Europe PMC
Risks, side effects and study doses are only published on hand-reviewed profiles. Want this one reviewed, or spotted something wrong? Tell us.