The study drug is a potential new treatment for Friedreich’s Ataxia (FA)
The Nervous System Study aims to evaluate the safety and tolerability of a new investigational treatment for Friedreich’s Ataxia in healthy volunteers. Your participation will help us gather crucial data to advance our research and move closer to a potential treatment for FA.
Friedreich’s ataxia (FA) is a rare genetic disease that typically begins in childhood, between the ages of 5 and 15. It affects movement, speech, and daily activities. Over time, FA can lead to a loss of mobility and other serious health issues such as heart problems and diabetes, often shortening life expectancy to the 30s or 40s.
Clinical Trial Details:
Call us on 1800 243 733 to discuss your eligibility today!