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● TERIPARATIDEBone peptide

Compound dossier · evidence, sources, and tracked market

Teriparatide

Bone peptide Strong evidence 0 cited studies 0 tracked vendors

A parathyroid-hormone fragment studied in research on bone-metabolism pathways.

Evidence brief

Teriparatide is a recombinant fragment of human parathyroid hormone (rhPTH 1-34) approved as an anabolic (bone-forming) osteoporosis medicine, and it has been studied in many randomized controlled trials and pooled in meta-analyses.

Published dosing & study context → Reconstitution calculator →

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▸ Regulatory status USapprovedEUapprovedUKapproved

An approved prescription medicine for osteoporosis: FDA-approved as Forteo (NDA 021318) for postmenopausal women and men at high risk of fracture and for glucocorticoid-induced osteoporosis, centrally authorised in the EU as Forsteo, and authorised in the UK. Approved for osteoporosis only — not for any performance, recovery or anti-ageing use. Research use only — not medical advice.

Sources: Forteo (teriparatide) prescribing information · DailyMed checked 2026-08-15 · EMA · Forsteo EPAR checked 2026-08-15

● Research articles about Teriparatide All research →

Published dosing for Teriparatide

Source-linked reference figures with the population and study context alongside each amount. Study arms are not a starting dose, titration schedule, or personal treatment plan. Label records refer to the named approved medicine, not vendor products.

Titration schedule card. Teriparatide (Hypoparathyroidism study (PMID 33538953)) titration as published, Peer-reviewed: Start: 20 µg daily, 5-7 weeks; May increase to: 20 µg twice daily, 7-17 weeks. Source: PMID 33538953. Research use only. Studied in: human · 12 adults with chronic hypoparathyroidism not well controlled on calcium and calcitriol · phase III open-label non-comparative study (3 months).
Hypoparathyroidism study (PMID 33538953). Titration schedule exactly as PMID 33538953 ↗ published it, step for step. pepmg does not compose or adjust schedules. Save the card: landscape · portrait

Dose administered in a phase 3 randomised double-blind active-controlled trial (human, postmenopausal women aged 50-80 with osteoporosis)

20 mcg once daily

human · postmenopausal women aged 50-80 with osteoporosis · phase 3 randomised double-blind active-controlled trial · Route reported: subcutaneous

Read original source: PMID 40620511 ↗

Dose administered in a randomised trial (Fracture Prevention Trial analysis) (human, postmenopausal women with osteoporosis, including mild or moderate renal impairment)

20 mcg/day or 40 mcg/day

human · postmenopausal women with osteoporosis, including mild or moderate renal impairment · randomised trial (Fracture Prevention Trial analysis) · Route reported: subcutaneous

Read original source: PMID 17013567 ↗

Research use only — this reports what an FDA label or a peer-reviewed study published, tied to its species and study context. It is not medical advice, not a recommendation to use, and no dose here is generated by pepmg. Any dosing decision is for a qualified professional. Animal-study amounts do not establish a human dose.

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Reconstitution calculator → · Converts your entered quantities; it does not select a dose or establish suitability for use.

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→ Reconstitution calculator for Teriparatide research math.
All products listed are sold by third-party vendors for laboratory and research use only (RUO). Where an FDA label or a peer-reviewed study has published a dose, pepmg reports it with the source named, because that is safer than guessing. It is a report, not medical advice and not a recommendation to use anything. pepmg sells nothing and ships nothing. Listings are price-tracking data, not endorsements.