News

US Food and Drug Administration Commissioner Marty Makary said he’s trying to persuade Vinay Prasad, the agency’s former head ...
Sarepta Therapeutics (NASDAQ:SRPT) has hired a lobbying firm with close ties to the Trump administration as regulatory ...
CGT Global, a leading biotechnology company driving the development and delivery of innovative cell and gene therapies, today ...
A 26-year-old Downriver man seen at Children’s Hospital of Michigan in Detroit since infancy for a rare bleeding disorder in ...
Currently, GenAns Biotech is conducting investigator-initiated trials for several gene therapies, including GA001 for ...
The primary safety risks associated with gene therapy include immune reactions and off-target effects in unintended organs, ...
The Revell family hoped a gene therapy could buy time for their sons, who have a rare and fatal disease. After two patients ...
Parents of boys with Duchenne muscular dystrophy weigh in on drug innovation and medical regulation.
The drug, which was designed to treat Duchenne muscular dystrophy, has been linked to the deaths of two teenage boys.
Gene therapy has been headline news in recent years, in part due to the rapid development of biotechnology that enables doctors to administer such treatments. Broadly, gene therapies are ...
Gene therapy appears to be a promising approach for a subset of genetic deafness, although challenges remain with development ...
Leveraging Northway Biotech’s 20+ years of CDMO expertise, Diorasis Therapeutics is advancing AAV gene therapy for glaucoma ...