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axelvento

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axelvento

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Thursday, 12/21/2023 9:42:17 AM

Thursday, December 21, 2023 9:42:17 AM

Post# of 700032
-countdown -The MAA seeks approval for commercialization of DCVax-L for both newly diagnosed and recurrent glioblastoma (GBM). The application also requests to be considered under the MHRA's rapid 150-day review pathway, which the agency has established for new medicines for serious unmet medical needs.
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