Web22 Jun 2024 · But the impetus for the nonprofit and company was largely personal: Horgan hopes to find a treatment for his brother, Terry, 23, who has a genetic mutation that causes Duchenne muscular dystrophy. Web17 Aug 2024 · Terry Horgan in 2024. Later this year, Horgan will receive a genetic therapy custom-designed to treat his unique form of Duchenne muscular dystrophy. Sydney …
Upstate NY man in CRISPR gene therapy study dies
Web4 Nov 2024 · Terry Horgan, a 27-year-old who had Duchenne muscular dystrophy, died last month, according to Cure Rare Disease, a Connecticut-based nonprofit founded by his … Web2 Mar 2024 · Rich Horgan is the Founder and President of Cure Rare Disease. He has a deep passion for Duchenne muscular dystrophy (DMD) and other rare diseases. With a younger brother impacted by DMD, Rich... brewmaster monk secondary stats
More than 200 people have been treated with experimental …
WebMeet our seventh disruptor Rich Horgan. Find out how Rich and his team at Cure Rare Disease are accelerating tailored, life-saving therapies for people with ... Web21 Sep 2024 · NEW HAVEN, Conn. — Terry Horgan is a 26-year-old who works at Cornell University. He’s very tech savvy. Currently, he gets around in a motorized wheelchair due … Web7 Nov 2024 · Less than 2 months after the FDA gave Cure Rare Disease the go-ahead to proceed with its N-of-1 clinical trial (NCT0551429) assessing its CRISPR-based gene … brewmaster monk rotation dragonflight