- cafead   Oct 01, 2021 at 11:12: AM
via The FDA on Thursday accidentally published a notice announcing the award of a priority review voucher to rare disease drug developer Enzyvant for its new regenerative therapy for the treatment of pediatric patients with congenital athymia.
The only problem? The treatment still hasn’t won FDA approval.
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The only problem? The treatment still hasn’t won FDA approval.
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