Ten of 11 children born with a rare form of congenital hearing loss experienced improvements after receiving the company’s ...
The funding will accelerate the development of Fuse's technology platform and pipeline of novel gene therapies. With its ...
1 日
IFLScience on MSNNew Gene Therapy “Life Changing” For Kids With Severe Form Of BlindnessFour children born with a rare genetic form of severe blindness have all experienced significant improvements in their ...
A gene therapy from Regeneron Pharmaceuticals Inc. improved hearing in nearly all deaf children in a clinical trial, results ...
Revolutionary gene therapy approaches show promise in treating various retinal conditions, potentially transforming treatment ...
Hyderabad: Cell and gene therapy solutions provider Miltenyi Biotec on Monday announced the roll-out of what is touted as ...
OTO, is one of several early-stage gene therapies being developed to treat relatively straight-forward causes of genetic ...
Pfizer is pulling further away from the gene therapy field with its decision to discontinue hemophilia product Beqvez. | ...
An experimental trial of gene therapy has helped four toddlers - born with one of the most severe forms of childhood ...
12 時間
GlobalData on MSNSuccess for YolTech’s hyperoxaluria in vivo gene therapy in early-stage trialYolTech's gene therapy is intended as a one-time life-long cure for patients living with PH1, which can lead to kidney ...
4 日
IFLScience on MSNInhalable Cystic Fibrosis Gene Therapy 24 Years In The Making Enters Clinical TrialsA new inhalable gene therapy for cystic fibrosis (CF) has entered Phase I clinical trials, a major milestone on the journey ...
A Connecticut boy is among four children all born with severe childhood blindness who gained “life-changing improvements” to ...
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