FDA grants rolling review for Palvella QTORIN rapamycin NDA in microcystic lymphatic malformations

Palvella Therapeutics, Inc.

Palvella Therapeutics, Inc.

PVLA

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  • Palvella Therapeutics received FDA rolling review for its QTORIN rapamycin NDA in microcystic lymphatic malformations.
  • NDA submission remains targeted for the second half of 2026.
  • Program holds FDA Breakthrough Therapy, Fast Track, and Orphan Drug designations.


Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Palvella Therapeutics Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 202606220730PRIMZONEFULLFEED9750298) on June 22, 2026, and is solely responsible for the information contained therein.

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