A bespoke CRISPR therapy suggests a blueprint for treating ‘N-of-1’ diseases
A gene editing drug custom-made for a critically ill baby showed that, for some ultra-rare diseases, it’s possible to design and test a new CRISPR medicine in just a few months.
New: A #CRISPR gene editing drug custom-made for a critically ill baby in just a few months appeared to be safe and working as intended, according to results newly published in the New England Journal of Medicine. Details below:
#biotech #biosky #ASGCT2025
www.biopharmadive.com/news/crispr-...
15.05.2025 17:24
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First Prader-Willi drug to reduce hunger approved by FDA
Clearance of Vykat unlocks what analysts anticipate will be a lucrative market opportunity for Soleno Therapeutics.
FDA approves Soleno Therapeutics drug to treat the intense hunger associated with Prader-Willi syndrome.
The OK is a milestone for research into the rare disease, which has frustrated drugmakers' prior attempts. More from @benthefidler.bsky.social here:
www.biopharmadive.com/news/soleno-...
26.03.2025 21:20
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