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Palvella's drug showed strong results in rare lymphatic malformation trial, boosting shares and paving way for FDA submission.
Palvella Therapeutics' shares surged 33% after its Phase 3 SELVA trial showed QTORIN 3.9% rapamycin gel met primary and secondary endpoints in treating microcystic lymphatic malformations, a rare condition with no approved therapies.
The trial of 49 patients showed significant improvement, with 95% achieving at least a one-point gain on key assessments and 86% rated much or very improved.
The topical treatment was well-tolerated, with no serious drug-related side effects.
Palvella plans to file a New Drug Application with the FDA in late 2026, potentially leading to approval by early 2027.
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El medicamento de Palvella mostró fuertes resultados en el ensayo de malformación linfática rara, aumentando las acciones y allanando el camino para la presentación de la FDA.