
Fragile X Syndrome Research & Treatment • FRAXA Research Foundation - Finding a Cure for Fragile X
43222167
1994
Newburyport, MA 01950 USA
fraxa.org
fraxaresearch
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News

What research is FRAXA funding in 2025? Join us for a live webinar where FRAXA Co-Founders Dr. Michael Tranfaglia and Katie Clapp will present an overview of all Fragile X research grants awarded so far this year. From novel therapeutic strategies to innovative models of Fragile X syndrome, each project represents a step forward in our mission to accelerate effective treatments. Whether you’re a scientist, clinician, or part of the Fragile X community, this session offers a comprehensive view of where the field is heading — and who’s driving it. » Learn what’s being funded » Understand research priorities » Get your questions answered in real time #FragileX #NeuroscienceResearch #RareDiseaseInnovation (fb)

Dr. Jeannie Lee, a leading researcher at Harvard Medical School and Massachusetts General Hospital, has been awarded a $1 million Blavatnik Therapeutics Challenge Award to expand her innovative work reactivating the gene that fails to function in Fragile X syndrome. This award builds on years of research funded by FRAXA and is one of the most competitive funding programs at Harvard Medical School, designed to fast-track promising science toward real-world treatments. It also means that FRAXA can fund the next essential steps in Dr. Lee’s research. Stay tuned! #FragileX #TranslationalResearch (fb)

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About the organization
- 978, G80, H80, G48 -
FRAXA Research Foundation Finding a Cure for Fragile X Syndrome Accelerating Fragile X Research for Effective Treatments Discovering Effective Treatments A Cure for Fragile X Syndrome Your support enables FRAXA Research Foundation to fund groundbreaking research and lifechanging clinical trials. How Does FRAXA Help. FRAXAs mission is to find effective treatments and ultimately a cure for Fragile X syndrome. We directly fund research grants and fellowships at top universities around the world.
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