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Bone Health
Clinical

Parathyroid Hormone (rhPTH 1-84)

Also known as: Natpara, Natpar, rhPTH(1-84), Parathyroid hormone

Recombinant full-length human PTH, FDA-approved in 2015 as Natpara for hypoparathyroidism. Manufacturing was discontinued at the end of 2024.

Last updated

Mechanism of Action

Recombinant human parathyroid hormone (1-84) is identical to the 84-amino-acid hormone made by the parathyroid glands. Acting on PTH1R in kidney and bone, it increases renal calcium reabsorption, promotes activation of vitamin D (1,25-dihydroxyvitamin D) to raise intestinal calcium absorption, and increases phosphate excretion. In hypoparathyroidism this replaces the missing hormone and reduces the need for high-dose calcium and active vitamin D.

Half-life
~3 hours (subcutaneous)
Administration Routes
Subcutaneous
Research Status
Clinical

Reported Benefits

  • Maintained serum calcium while reducing oral calcium and active vitamin D needs (REPLACE trial)
  • Lowers urinary calcium and serum phosphate in hypoparathyroidism
  • Long-term data on bone and biochemical effects over years of use

Potential Side Effects

  • Boxed warning: osteosarcoma seen in rat studies
  • Hypocalcemia and hypercalcemia, especially when doses change or stop
  • Paresthesia, headache, nausea and muscle cramps
  • Diarrhea and joint pain

Common Dosing

Labeled dosing started at 50 mcg injected subcutaneously into the thigh once daily, adjusted in steps while monitoring serum calcium, with calcium and active vitamin D tapered accordingly. Because manufacturing ended in 2024, new patients are generally not started on it. 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, unexplained alkaline phosphatase elevation)
  • Hypoparathyroidism caused by calcium-sensing receptor activating mutations (not studied)
  • Acute post-surgical hypoparathyroidism (not studied)

No documented stacking partners for Parathyroid Hormone (rhPTH 1-84) yet.

  • Efficacy and safety of recombinant human parathyroid hormone (1-84) in hypoparathyroidism (REPLACE): a double-blind, placebo-controlled, randomised, phase 3 study

    2013

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  • The Clinical and Skeletal Effects of Long-Term Therapy of Hypoparathyroidism With rhPTH(1-84)

    2023

    View
  • Open-label extension of a randomized trial investigating safety and efficacy of rhPTH(1-84) in hypoparathyroidism

    2024

    View

Natpara was FDA-approved in January 2015 as an adjunct to calcium and vitamin D for hypoparathyroidism, under a restricted REMS program. It was recalled in the US in 2019 over rubber particulates, and in 2022 Takeda announced it would stop manufacturing it worldwide at the end of 2024, supplying remaining stock until depleted. As of 2026 it is effectively no longer available for new patients.

In August 2024 the FDA approved palopegteriparatide (Yorvipath), a long-acting PTH(1-34) prodrug, for adults with hypoparathyroidism. Switching between therapies is managed by an endocrinologist under medical supervision.

rhPTH(1-84) is the full 84-amino-acid hormone, while teriparatide is the active 34-amino-acid fragment. Teriparatide is approved for osteoporosis, not hypoparathyroidism.

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.