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Congratulations to Vertex Pharmaceuticals and CRISPR Therapeutics for achieving the first-ever MHRAgovuk approval of a #CRISPR therapy. This historic milestone is paving the way for the future of #geneediting.

Intellia Therapeutics

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16,935 次观看 • 2 年前 •via X (Twitter)

健康养生科学技术 #CRISPR #geneediting

Anya Rossi• Live Now

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Great way to wrap up a historic week! We’re honored to light up the iconic Nasdaq Tower in Times Square celebrating Intellia's recent #CRISPR milestone. A big thanks to Nasdaq for recognizing our recent HAELO topline data, a first ever for in vivo #geneediting.

Great way to wrap up a historic week! We’re honored to light up the iconic Nasdaq Tower in Times Square celebrating Intellia's recent #CRISPR milestone. A big thanks to Nasdaq for recognizing our recent HAELO topline data, a first ever for in vivo #geneediting.

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CHOP & Penn Medicine have delivered the first-ever personalized gene editing therapy for a patient with CPS1 deficiency, marking a major milestone in the application of CRISPR-based treatments. Learn more about KJ & the future of personalized medicine:

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They knew from the beginning that mRNA was gene editing technology, and NOT a vaccine. The whole thing was a lie. Don't believe me? Listen to the president of Bayer pharmaceuticals tell you himself. #VaccineDeath #StoptheShotsNow #GeneEditing #CRISPR

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Johnny Lubin was one of the youngest patients in the clinical trial supporting today’s approval of the first CRISPR treatment in the US, one of two therapies approved today for sickle cell. He told us how the therapy has changed his life:

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Alyssa is a 13-year old British girl who has #leukemia.This brave girl is the first person to ever receive a #BaseEditing treatment which led to a complete remission of #Cancer 6 months later! #CRISPR & #GeneEditing give hope to so many! David R. Liu @beamtx

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“I don’t think it’s exaggerating to say that this is the future of medicine.” For years, Dr. Rebecca Ahrens-Nicklas treated babies with rare genetic diseases knowing palliative care was often the only option. In 2023, she partnered with gene-editing researcher Dr. Kiran Musunuru to try something new: using CRISPR to correct disease-causing mutations before the damage became irreversible. In 2025, doctors delivered the first successful personalized CRISPR therapy, pointing to a future where gene therapies are custom-built for patients who once had no options. See the full TIME100 Health list of leaders, scientists, doctors, and more here:

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