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FDA fast-tracks Snipr Biome's primary candidate

Snipr Biome’s CRISPR treatment of blood infections in cancer patients has been granted special status by the US Food and Drug Administration.

Photo: Snipr Biome/PR

Just two weeks after the FDA approved the development plans for Snipr Biome’s candidate, SNIPR001, the company now reveals it has been awarded fast-track status.

”At Snipr Biome, we are extremely proud to have been granted fast-track designation by the FDA. It underlines SNIPR001’s potential to be a game-changer for hematological cancer patients at increased risk of life-threatening bloodstream infections caused by E. coli,” says Christian Grøndahl, co-founder & CEO of the firm.

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