Palvella Therapeutics to Report Q3 Results, Highlight Progress in Rare Skin Disease Trials

Palvella Therapeutics

WAYNE, PAPalvella Therapeutics, Inc. (Nasdaq: PVLA) announced it will report third-quarter 2025 financial results before markets open on Tuesday, November 11, 2025. Company leadership will host a live investor conference call at 8:30 a.m. ET to review financial performance and provide a corporate update.

Investors can access the live webcast and presentation slides via the “Events & Presentations” section of Palvella’s website. Those who prefer to join by phone can register for dial-in details, and a replay of the webcast will be available for 90 days following the event.

Palvella Therapeutics, a clinical-stage biopharmaceutical company focused on rare dermatologic diseases, continues to advance its QTORIN™ platform — a proprietary delivery system designed for serious, lifelong skin conditions that currently lack approved treatments. The company’s lead candidate, QTORIN 3.9% rapamycin anhydrous gel (QTORIN™ rapamycin), is being evaluated across multiple late-stage studies.

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The pivotal Phase 3 SELVA trial is investigating QTORIN™ rapamycin in patients with microcystic lymphatic malformations, while the ongoing Phase 2 TOIVA trial is evaluating its potential in cutaneous venous malformations. A Phase 2 study in clinically significant angiokeratomas is also planned.

Founded by experts in rare disease drug development, Palvella aims to commercialize first-in-class therapies for serious skin disorders with limited treatment options. The company noted that QTORIN™ rapamycin remains an investigational product and has not been approved by the U.S. Food and Drug Administration or other regulatory authorities for any indication.

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