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CRISPR Therapeutics Says FDA Grants RMAT Designation To CTX130
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(RTTNews) - Biopharmaceutical company CRISPR Therapeutics (CRSP) announced Wednesday that the U.S. Food and Drug Administration (FDA) granted Regenerative Medicine Advanced Therapy (RMAT) designation to CTX130, the Company's wholly-owned allogeneic CAR T cell therapy targeting CD70, for the treatment of Mycosis Fungoides and Sézary Syndrome (MF/SS).
Established under the 21st Century Cures Act, RMAT designation is a dedicated program designed to expedite the drug development and review processes for promising pipeline products, including genetic therapies.
Similar to Breakthrough Therapy designation, RMAT designation provides the benefits of intensive FDA guidance on efficient drug development.
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Japan Unemployment Data Due On Friday
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Swiss Market Closes On Firm Note
The Switzerland market closed on a firm note on Thursday, after trading positive right through the day's trading session, amid rising expectations about more monetary easing by the Federal Reserve and easing concerns about the government shutdown in the U.S.
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Major European Markets Close On Bright Note
European stocks closed on a firm note on Thursday, with several markets climbing to multi-month highs, as optimism over monetary easing by the Federal Reserve in the coming months, hopes around artificial intelligence, helped outweigh concerns about a partial U.S. government shutdown.
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Bay Street Likely To Open On Mixed Note
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