Higher dose hormone therapy aims to control rare calcium disorder

NCT ID NCT07081997

First seen Nov 01, 2025 · Last updated Jun 23, 2026 · Updated 33 times

Summary

This phase 3 trial tests higher daily doses (over 30 mcg) of palopegteriparatide (Yorvipath) in 36 adults with chronic hypoparathyroidism. Participants already on the drug will have their dose adjusted to find the best level for controlling calcium without needing extra vitamin D or calcium supplements. The study lasts 78 weeks and focuses on safety and effectiveness.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • Ascendis Pharma Investigational Site

    RECRUITING

    Reno, Nevada, 89511, United States

  • Ascendis Pharma Investigational Site

    RECRUITING

    New York, New York, 10032, United States

  • Ascendis Pharma Investigational Site

    RECRUITING

    Spokane Valley, Washington, 99216, United States

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance

palopegteriparatide (Yorvipath)

What this could lead to

If successful, this could provide a more effective way to manage hypoparathyroidism with higher doses, reducing the need for calcium and vitamin D supplements.

What could go wrong

This is a small, open-label trial with only 36 participants, so results may not apply broadly. Higher doses may also increase side effects.

Conditions

The condition(s) this trial relates to.

endocrine system disorder hypoparathyroidism parathyroid gland disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.