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Palvella Therapeutics, Inc. - Common Stock (NQ:PVLA)

96.17 -1.84 (-1.87%)
Streaming Delayed Price Updated: 11:51 AM EST, Jan 21, 2026 Add to My Watchlist
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Press Releases about Palvella Therapeutics, Inc. - Common Stock

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Palvella Therapeutics Provides Corporate Update and 2026 Outlook: Advancing a Late Clinical-Stage Pipeline and Platform to Address Multiple Serious, Rare Skin Diseases and Vascular Malformations with No FDA-Approved Therapies
From Palvella Therapeutics Inc.
Via GlobeNewswire
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Palvella Therapeutics Strengthens Leadership Team with Appointment of Veteran Medical Affairs Leader Vimal Patel, PharmD, as Senior Vice President of Medical Affairs
From Palvella Therapeutics Inc.
Via GlobeNewswire
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Palvella Therapeutics Granted FDA Fast Track Designation for QTORIN™ 3.9% Rapamycin Anhydrous Gel (QTORIN™ rapamycin) for the Treatment of Angiokeratomas
From Palvella Therapeutics Inc.
Via GlobeNewswire
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Palvella Therapeutics Announces Positive Topline Results from Phase 2 TOIVA Clinical Trial of QTORIN™ 3.9% Rapamycin Anhydrous Gel (QTORIN™ rapamycin) for the Treatment of Cutaneous Venous Malformations, a Serious, Rare Genetic Disease with No
From Palvella Therapeutics Inc.
Via GlobeNewswire
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Palvella Therapeutics Reports Third Quarter 2025 Financial Results and Provides Corporate Update
From Palvella Therapeutics Inc.
Via GlobeNewswire
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Palvella Therapeutics to Present at the Stifel 2025 Healthcare Conference
From Palvella Therapeutics Inc.
Via GlobeNewswire
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Palvella Therapeutics Announces New QTORIN™ Product Candidate, QTORIN™ Pitavastatin, for the Treatment of Disseminated Superficial Actinic Porokeratosis (DSAP), a Rare, Chronic, and Pre-Cancerous Genetic Skin Disease with No FDA-Approved Therapies
From Palvella Therapeutics Inc.
Via GlobeNewswire
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Palvella Therapeutics to Host Third Quarter 2025 Financial Results and Corporate Update Conference Call on November 11, 2025
From Palvella Therapeutics Inc.
Via GlobeNewswire
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U.S. Food and Drug Administration Awards Year Two Proceeds from Orphan Products Grant Supporting Palvella Therapeutics’ Phase 3 SELVA Trial of QTORIN™ Rapamycin for Microcystic Lymphatic Malformations
From Palvella Therapeutics Inc.
Via GlobeNewswire
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Palvella Therapeutics Announces Expansion of QTORIN™ Rapamycin’s Development into Clinically Significant Angiokeratomas, a Rare, Chronically Debilitating Lymphatic Disease with No FDA-approved Therapies
From Palvella Therapeutics Inc.
Via GlobeNewswire
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Palvella Therapeutics Announces Scientific Publication in Lymphatic Research and Biology Highlighting Recent Advances in the Pathogenesis of Venous Malformations and the Real-World Use of Rapamycin as an Emerging Targeted Therapy
From Palvella Therapeutics Inc.
Via GlobeNewswire
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Palvella Therapeutics Completes Enrollment in Phase 2 TOIVA Trial of QTORIN™ Rapamycin for Cutaneous Venous Malformations
From Palvella Therapeutics Inc.
Via GlobeNewswire
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Palvella Therapeutics Strengthens Leadership with Appointment of Accomplished Scientist and Biopharmaceutical Executive David W. Osborne, Ph.D. as Chief Innovation Officer
From Palvella Therapeutics Inc.
Via GlobeNewswire
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Palvella Therapeutics to Present at Upcoming Healthcare Investor Conferences
From Palvella Therapeutics Inc.
Via GlobeNewswire
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Palvella Therapeutics Reports Second Quarter 2025 Financial Results and Provides Corporate Update
From Palvella Therapeutics Inc.
Via GlobeNewswire
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Palvella Therapeutics to Host Second Quarter 2025 Financial Results and Corporate Update Conference Call on August 14, 2025
From Palvella Therapeutics Inc.
Via GlobeNewswire
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Palvella Therapeutics to Participate in the Canaccord Genuity 45th Annual Growth Conference
From Palvella Therapeutics Inc.
Via GlobeNewswire
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Palvella Therapeutics Added to Russell 3000® and Russell 2000® Indexes
From Palvella Therapeutics Inc.
Via GlobeNewswire
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Palvella Therapeutics Completes Enrollment in Phase 3 SELVA Trial of QTORIN™ Rapamycin for Microcystic Lymphatic Malformations, Exceeding Enrollment Target by Over 25%
From Palvella Therapeutics Inc.
Via GlobeNewswire
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Palvella Therapeutics Granted Sixth U.S. Patent Covering 0.1–20% Anhydrous Compositions of Rapamycin and Other mTOR Inhibitors
From Palvella Therapeutics Inc.
Via GlobeNewswire
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Palvella Therapeutics Receives Initial Proceeds from FDA Orphan Products Grant to Support Phase 3 SELVA Trial of QTORIN™ Rapamycin for Microcystic Lymphatic Malformations
From Palvella Therapeutics Inc.
Via GlobeNewswire
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Palvella Therapeutics Strengthens Executive Leadership Team with Appointment of Rare Disease Commercial Veteran Ashley Kline as Chief Commercial Officer
From Palvella Therapeutics Inc.
Via GlobeNewswire
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Palvella Therapeutics Reports First Quarter 2025 Financial Results and Provides Corporate Update
From Palvella Therapeutics Inc.
Via GlobeNewswire
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Palvella Therapeutics to Host First Quarter 2025 Financial Results and Corporate Update Conference Call on May 15, 2025
From Palvella Therapeutics Inc.
Via GlobeNewswire
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Palvella Therapeutics to Ring the Nasdaq Opening Bell on May 12, 2025
From Palvella Therapeutics Inc.
Via GlobeNewswire
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Palvella Therapeutics Announces Abstract Highlighting the Estimated Diagnosed Prevalence and Annual Incidence of Lymphatic Malformations in the U.S. Accepted for Poster Presentation at the 82nd Annual Meeting of the Society for Investigative Dermatology
From Palvella Therapeutics Inc.
Via GlobeNewswire
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Palvella Therapeutics Granted Additional U.S. Patent for QTORIN™ Rapamycin for the Treatment of Microcystic Lymphatic Malformations
From Palvella Therapeutics Inc.
Via GlobeNewswire
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Palvella Therapeutics Announces QTORIN™ Rapamycin 3.9% Anhydrous Gel for the Treatment of Microcystic Lymphatic Malformations Featured in Oral Presentation by Amy Paller, M.S., M.D., Chair of Dermatology at Northwestern University’s Feinberg School of
From Palvella Therapeutics Inc.
Via GlobeNewswire
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Palvella Therapeutics to Present at the Jones Healthcare and Technology Innovation Conference
From Palvella Therapeutics Inc.
Via GlobeNewswire
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Palvella Therapeutics Announces Late-Breaking Oral Presentation at the 15th World Congress of Pediatric Dermatology
Presentation to highlight SELVA, a 24-week, Phase 3, single-arm, baseline-controlled clinical trial of QTORIN™ rapamycin 3.9% anhydrous gel for the treatment of microcystic lymphatic malformations 
From Palvella Therapeutics Inc.
Via GlobeNewswire
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