Palvella Therapeutics, Inc (PVLA NASDAQ) stock market data APIs
$90.1083
-3.33(-3.7%)
as of January 6, 2026
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Palvella Therapeutics, Inc Financial Data Overview
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Palvella Therapeutics, Inc., a clinical-stage biopharmaceutical company, focuses on developing and commercializing novel therapies to treat patients serious and rare genetic skin diseases. The company's lead product candidate is QTORIN 3.9% rapamycin anhydrous gel that is in Phase 3 clinical trial for the treatment of microcystic lymphatic malformations, as well as in Phase 2 clinical trial to treat cutaneous venous malformations. It also develops QTORIN rapamycin for the treatment of other mTOR-driven skin diseases. The company is based in Wayne, Pennsylvania
Prev. Close
90.1083
Open
86.7773
High
90.5081
Low
83.3707
52 wk Range
12.02-114.69
Market Cap
1 070 M
Shares Outstanding
11 836 K
EPS
-1.03
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Palvella Therapeutics, Inc News
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High Analyst Confidence on Palvella Therapeutics (PVLA) Following Encouraging Phase 2 Data for QTORIN Rapamycin
With strong 1-year returns and upside potential, Palvella Therapeutics, Inc. (NASDAQ:PVLA) secures a spot on our list of the 12 best multibagger stocks to buy heading into 2026.High Analyst Confidence...
Palvella Therapeutics price target raised to $200 from $120 at Oppenheimer
Oppenheimer raised the firm’s price target on Palvella Therapeutics (PVLA) to $200 from $120 and keeps an Outperform rating on the shares after the company reported the Phase 2 TOIVA readout for Qto...
Palvella Therapeutics Reports Positive Phase 2 Results For QTORIN Rapamycin Gel
(RTTNews) - Palvella Therapeutics, Inc. (PVLA) on Monday announced positive topline results from its Phase 2 TOIVA study of QTORIN 3.9% rapamycin anhydrous gel for the treatment of cutaneous venous ma...
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 FDA-approved Therapies
73% of trial participants (11/15 participants) improved on the Overall Cutaneous Venous Malformations Investigator Global Assessment (Overall cVM-IGA) at Week 12; 67% of trial participants (10/15 part...
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