First human trial launches for Ultra-Rare bone disorder
NCT ID NCT07541209
First seen May 06, 2026 · Last updated May 21, 2026 · Updated 4 times
Summary
This study tests a new drug, PTH-IA, for Jansen's metaphyseal chondrodysplasia (JMC), a very rare genetic bone disease affecting about 30 people worldwide. JMC causes severe short stature, frequent fractures, bone pain, and kidney problems. The drug aims to block overactive signals in bone and kidney cells. The trial will enroll 12 adults and children to check safety, dosing, and early effects.
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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.
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
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
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Contact
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Locations
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National Institutes of Health Clinical Center
RECRUITINGBethesda, Maryland, 20892, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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