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Bone Health
Clinical

Palopegteriparatide

Also known as: Yorvipath, TransCon PTH

A long-acting PTH(1-34) prodrug FDA-approved in 2024 as Yorvipath for hypoparathyroidism in adults. Prescription medication.

Last updated

Mechanism of Action

Palopegteriparatide is teriparatide, PTH(1-34), transiently linked to a methoxy-polyethylene glycol carrier through Ascendis Pharma's TransCon linker. After once-daily subcutaneous injection the linker cleaves slowly, releasing active PTH(1-34) to give steady PTH levels across 24 hours. Continuous PTH1R activation in kidney and bone restores calcium reabsorption, vitamin D activation and phosphate excretion, replacing the missing hormone.

Half-life
~60 hours (released PTH)
Administration Routes
Subcutaneous
Research Status
Clinical

Reported Benefits

  • Normal serum calcium without conventional active vitamin D or high-dose calcium in most PaTHway patients
  • Lowers urinary calcium excretion
  • Improved kidney function (eGFR) in phase 3 follow-up
  • Improved hypoparathyroidism-related quality-of-life scores

Potential Side Effects

  • Injection-site reactions
  • Headache, flushing, dizziness and orthostatic hypotension
  • Hypercalcemia and hypocalcemia, especially during titration or after stopping
  • Potential osteosarcoma risk based on animal data (warning)

Common Dosing

Labeled dosing starts at 18 mcg injected subcutaneously once daily and is adjusted in small steps based on serum calcium, while conventional calcium and active vitamin D are tapered. It comes in prefilled dose-adjustable pens. Dosing is set and supervised by the prescribing clinician.

The dosing information above is aggregated from research literature and anecdotal community reports for educational purposes only. It is not a recommendation, prescription, or medical advice. Peptides are sold as research chemicals only and are not intended for human use.

Contraindications

  • Increased osteosarcoma risk (Paget's disease, open epiphyses, prior skeletal radiation): weigh carefully
  • Acute post-surgical hypoparathyroidism (not evaluated)
  • Digoxin use requires closer calcium monitoring

No documented stacking partners for Palopegteriparatide yet.

  • PaTH Forward: A Randomized, Double-Blind, Placebo-Controlled Phase 2 Trial of TransCon PTH in Adult Hypoparathyroidism

    2022

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  • Efficacy and Safety of Parathyroid Hormone Replacement With TransCon PTH in Hypoparathyroidism: 26-Week Results From the Phase 3 PaTHway Trial

    2023

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  • Efficacy and Safety of TransCon PTH in Adults With Hypoparathyroidism: 52-Week Results From the Phase 3 PaTHway Trial

    2025

    View

Yes. The FDA approved it as Yorvipath in August 2024 for adults with hypoparathyroidism, after an earlier 2023 complete response letter on manufacturing. It was approved in the European Union in November 2023 and is a prescription medication used under medical supervision.

Natpara was full-length PTH(1-84) with a roughly 3-hour half-life, giving a daily peak and trough. Palopegteriparatide releases PTH(1-34) slowly to keep PTH levels steadier over 24 hours, and Natpara manufacturing ended in 2024.

It releases teriparatide, PTH(1-34), but the carrier and linker make it a different product with different dosing and an approved indication of hypoparathyroidism rather than osteoporosis.

PeptideChat is for educational and research purposes only. Nothing on this site constitutes medical advice. Peptides are sold as research chemicals only and are not intended for human use. These statements have not been evaluated by the FDA and are not intended to diagnose, treat, cure, or prevent any disease. PeptideChat is an independent educational resource — not a pharmacy, compounding, or 503A/503B outsourcing facility — and does not sell products or provide medical advice.