Hope for rare aging disease: new drug targets bone loss
NCT ID NCT05847179
First seen Jan 26, 2026 · Last updated May 21, 2026 · Updated 19 times
Summary
This study tests a drug called Progerinin in 5 adults with Werner syndrome, a rare genetic condition that causes premature aging and bone loss. The goal is to see if the drug is safe and tolerable over one year. Participants take Progerinin twice daily, and researchers monitor side effects and bone density changes.
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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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Genom att skicka in godkänner du våra Användarvillkor
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Conditions
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