FDA (US): Approved (2015, Natpara) for hypocalcemia due to hypoparathyroidism; manufacturing discontinued by the manufacturer at the end of 2024 (no longer marketed).
EMA (EU): Approved (2017, Natpar, conditional authorization) for chronic hypoparathyroidism; manufacturing discontinued in 2024 and withdrawal of the authorization planned for July 1, 2026. Previously, Preotact (2006) was authorized for postmenopausal osteoporosis and was withdrawn.
Start with 50 µg subcutaneously daily, adjusting according to calcium up to 25–100 µg/day (REPLACE trial and FDA Natpara label). It should no longer be started in new patients.
With digoxin, calcium changes increase the risk of toxicity.
REPLACE RCT with 134 adults over 24 weeks: 53% reduced oral calcium and active vitamin D by at least half while keeping calcium in range, versus 2% with placebo.
View the study (RCT) →It is the complete 84-amino-acid parathyroid hormone. It raises blood calcium by releasing it from bone, increasing its reabsorption in the kidney, and activating vitamin D. In hypoparathyroidism it replaces the missing hormone.
In people
Information, not medical advice. Prescription or unapproved peptides should only be used under medical supervision.