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4 days ago · Since its founding, FAST had a vision to disrupt the traditional research model and create an innovative drug development culture to advance therapeutic discovery for Angelman syndrome (AS) and other like-disorders.
4 days ago · 4 June - After previously sharing that their son has a developmental issue, Stephanie Ho and Fred Cheng recently revealed that Asher was diagnosed with a rare severe genetic disorder called...
4 days ago · The company is creating a drug development ecosystem to bring transformative therapeutics to those living with Angelman syndrome (AS).
4 days ago · The company is creating a drug development ecosystem to bring transformative therapeutics to those living with Angelman syndrome (AS). "The team at FAST brought together expertise, experience...
4 days ago · Angelman syndrome is a rare genetic disorder caused by a malfunction in the UBE3A gene on chromosome 15. It leads to developmental delays, severe speech impairment, intellectual disability, and movement issues.
4 days ago · The Foundation for Angelman Syndrome Therapeutics (FAST) announced the establishment of an associated drug development accelerator called AS²Bio Inc. The company is creating a drug development ecosystem to bring transformative therapeutics to those living with Angelman syndrome (AS).
1 day ago · Angelman syndrome (AS) is a rare neurogenetic disorder that affects approximately one in 15,000 people – about 500,000 individuals worldwide. Children and adults with AS typically have impaired motor and balance, and debilitating seizures. Some individuals never walk. The majority do not speak.