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Fierce Pharma
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Research
Research
Boy with rare disease 'thriving' after 1st custom gene therapy
Born with a serious metabolic disease, scientists raced to prepare a custom CRISPR gene editing therapy for KJ in just six months.
Darren Incorvaia
May 15, 2025 1:00pm
VC firm to build biotech incubator in NJ life sciences complex
May 15, 2025 9:00am
Trump admin cuts $450M more from Harvard funding
May 13, 2025 1:33pm
Eli Lilly expands Purdue partnership with $250M investment
May 9, 2025 9:55am
NIH terminated $1.8B in grants in 40 days under Trump: study
May 9, 2025 3:04am
FDA plans to fully adopt generative AI by end of June
May 8, 2025 1:33pm