Fragile X Research: Current Treatment Trials and Progress Towards a Cure - Q&A Webinar (Nov 2023)

Join us in our FRAXA Research Foundation Q&A webinar from November 2023, focusing on cutting-edge developments in Fragile X research. Hosted by FRAXA Co-founders Dr. Mike Tranfaglia and Katie Clapp, this presentation and Q&A session dives deep into ongoing clinical trials and innovative research efforts in the progress towards a cure for Fragile X syndrome.

In this session, our hosts discuss exciting new gene reactivation strategies including Antisense Oligonucleotides (ASOs) and CRISPR. They also share experiences in current clinical trials. This webinar is an essential watch for families affected by Fragile X syndrome, researchers, and anyone interested in the latest scientific progress.

Discover the impact of these groundbreaking studies on the Fragile X community and gain a deeper understanding of the ongoing efforts to improve the lives of those affected by Fragile X syndrome.

#FragileX #FragileXResearch #ClinicalTrials #ASOs #GeneTherapy #ProteinReplacement #FRAXA #MedicalResearch

FRAXA’s 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. We partner with biomedical and pharmaceutical companies, large and small, to bridge the gap between research discoveries and actual treatments.

Treatments for Fragile X are likely to help people affected by autism, Alzheimer’s, and other brain disorders.

To learn more about FRAXA's Fragile X syndrome research, to get involved with Fragile X awareness and events or to donate to FRAXA research, visit www.fraxa.org

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