Palvella Therapeutics Announces Completion Of Rolling NDA Submission To FDA For QTORIN Rapamycin In Microcystic Lymphatic Malformations Under 505(b)(2) Pathway; FDA Filing Decision Expected Within 60 Days
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Why It Matters
Palvella finished sending its medicine paperwork to the FDA for a drug that treats a rare condition. The FDA will decide within two months if the medicine is safe and works well enough to use.
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