Solid said that the first patients to receive its Duchenne gene therapy all produced high levels of the target protein, an ...
Entrada Therapeutics can plough on with the development of its Duchenne muscular dystrophy (DMD) therapy, ENTR-601-44, now ...
The company raised $200 million after early findings hinted its therapy could be more potent than others like it, including ...
7h
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 ...
Entrada Therapeutics is finally able to get its Duchenne muscular dystrophy candidate (DMD) back on track after the FDA ...
Solid Biosciences has surged back into the Duchenne muscular dystrophy (DMD) gene therapy race. | Solid Biosciences has ...
Results show improved functional outcomes for people with Duchenne muscular dystrophy who are ambulatory. Elevidys, which is ...
Pfizer is pulling further away from the gene therapy field with its decision to discontinue hemophilia product Beqvez. | ...
Day 90 biopsy data reported from first 3 participants dosed in Phase 1/2 INSPIRE DUCHENNE trial —— Average microdystrophin expression of 110% ...
The scientists demonstrate that it is possible to specifically deliver the treatment to the muscle stem cells, avoiding ...
Solid Biosciences' SGT-003 gene therapy showed strong dystrophin expression, muscle health improvements, and no serious safety concerns in early trial data.
Solid Biosciences said Tuesday that the first three patients to receive its experimental gene therapy for Duchenne muscular dystrophy all produced high levels of microdystrophin, a miniature ...
Results that may be inaccessible to you are currently showing.
Hide inaccessible results