FDA releases draft guidance on genetic medicines
Prime Medicine welcomes framework enabling one approval for multiple mutations via in vitro data supplements, advancing rare disease treatments.
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Biotechnology company developing gene-editing therapies
primemedicine.comLast updated
In short: Prime Medicine dosed first Wilson patient, reported PM359 data, and replaced its CEO amid layoffs.
Prime Medicine welcomes framework enabling one approval for multiple mutations via in vitro data supplements, advancing rare disease treatments.
The investigational Prime Editor targets alpha-1 antitrypsin deficiency. Clinical data expected in 2027.
This clearance enables a global Phase 1/2 program. Prime Medicine expects to initiate the clinical study in late 2026 with initial data anticipated in 2027.
The clearance enables a global Phase 1/2 study targeting Wilson Disease mutations. Initial data is expected in 2027.
-- PM577a targets the H1069Q mutation in the ATP7B gene, the most prevalent WD-causing allele in North America and Europe -- -- Initiation of Phase...
-- Arbitration tribunal declared that PM647 is within Prime Medicine’s "Field”, confirming Prime Medicine’s right to develop and commercialize PM647 in AATD -- -- Prime...
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Prime Medicine (PRME) added ~8% in the premarket on Wednesday after an arbitration tribunal sided with the gene editing company in connection with a previously...
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