Quince Therapeutics advances Ataxia-Telangiectasia treatment with innovative AIDE platform, insider support, and NEAT Phase 3 ...

This was a double-blind ... presence of the gene-modified product, we have a window to treat the same patients with CORDstrom. But more importantly, CORDstrom is a systemic therapy, and as ...

A research team has developed and safely delivered a personalized gene editing therapy to treat an infant with a life-threatening, incurable genetic disease. The infant, who was diagnosed with the ...

Gyroscope Therapeutics and its gene therapy for the sight-robbing disease ... innovation in ophthalmology to treat and prevent blindness worldwide," she added. Gyroscope is one of the portfolio ...

Retinitis Pigmentosa (RP) is a type of inherited retinal diseases (IRDs) linked to mutations in over 100 different genes, leading to progressive vision loss that typically begins with night blindness ...

May 15, 2025 — A research team has developed and safely delivered a personalized gene editing therapy to treat an infant with a life-threatening, incurable genetic disease. The infant ...

This technique streamlines quality control in gene therapy vector production, potentially accelerating manufacturing and improving clinical outcomes. This summary was automatically generated using ...

SAN FRANCISCO, May 12, 2025 (GLOBE NEWSWIRE) -- Siren Biotechnology Inc., pioneers of Universal AAV Immuno-Gene Therapy for Cancer, today announced that it will present new scientific data at the 2025 ...

In RESTORE, a once-off administration of the gene therapy led to a “clinically meaningful” improvement in legally blind RP patients who had progressive and permanent neurodegeneration of the ...

The 11-year-old will be the first to receive an experimental antisense oligonucleotide gene therapy to treat NARS1 symptoms. “With her being the first, she’s going pioneer the way for a lot of ...

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