Palvella submits first NDA module for QTORIN rapamycin, dosing begins in angiokeratoma trial
The company says the rolling NDA submission stays on track for the second half of 2026, with a U.S. launch planned for early 2027 if approved.
SEC filing
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The company says the rolling NDA submission stays on track for the second half of 2026, with a U.S. launch planned for early 2027 if approved.
SEC filing