Palvella Therapeutics, Inc. (FRA:PI6)

Germany flag Germany · Delayed Price · Currency is EUR
124.00
+4.00 (3.33%)
Last updated: Jul 28, 2026, 8:01 AM CET
Market Cap1.79B +391.4%
Revenue (ttm)n/a
Net Income-42.76M
EPS-3.63
Shares Out n/a
PE Ration/a
Forward PEn/a
Dividendn/a
Ex-Dividend Daten/a
Volumen/a
Open124.00
Previous Close120.00
Day's Range124.00 - 124.00
52-Week Range31.40 - 136.00
Betan/a
Analystsn/a
Price Targetn/a
Earnings DateAug 6, 2026

About Palvella Therapeutics

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 rapamycin, a novel, 3.9% anhydrous topical 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 angiokeratomas and other mTOR-driven skin ... [Read more]

Industry Biological Products, Except Diagnostic Substances
CEO Wesley Kaupinen
Employees 29
Stock Exchange Frankfurt Stock Exchange
Ticker Symbol PI6

Financial Performance

Financial numbers in USD Financial Statements

News

Palvella Therapeutics to Host Second Quarter 2026 Financial Results and Corporate Update Conference Call on August 4, 2026

WAYNE, Pa., July 28, 2026 (GLOBE NEWSWIRE) -- Palvella Therapeutics, Inc . (Palvella or the “Company”) (Nasdaq: PVLA), a clinical-stage biopharmaceutical company focused on developing and commercializ...

3 hours ago - GlobeNewsWire

H.C. Wainwright says Palvella selloff ‘an overreaction’ to FDA’s BTD denial

H.C. Wainwright notes that on Monday, Palvella Therapeutics (PVLA) closed down 21% compared to the previous weeks close, which the firm believes was an overreaction to the updated corporate deck…

6 days ago - TheFly

Palvella Therapeutics selloff a buying opportunity, says BTIG

Palvella shares fell sharply after the FDA declined to grant Breakthrough Therapy Designation for QTORIN in cVMs, but the decision does not change the program’s strong clinical data, regulatory path,…

7 days ago - TheFly

Palvella Therapeutics falls -13.6%

Palvella Therapeutics (PVLA) is down -13.6%, or -$21.36 to $135.88.

7 days ago - TheFly

Palvella Therapeutics falls -9.0%

Palvella Therapeutics (PVLA) is down -9.0%, or -$14.11 to $143.13.

8 days ago - TheFly

Palvella Therapeutics appoints Savara CEO Matt Pauls to board

Palvella Therapeutics (PVLA) announced the appointment of Matt Pauls to its board of directors. Since 2020, he has served as chair of the board of directors and CEO of Savara…

4 weeks ago - TheFly

Palvella Therapeutics Appoints Accomplished Rare Disease Biotech Executive and Commercial Leader Matt Pauls, J.D., M.B.A., to Board of Directors

Brings more than 25 years of experience advancing and commercializing high-impact therapies for serious diseases, including those with limited or no approved treatment options

4 weeks ago - GlobeNewsWire

Palvella submits first rolling new drug application to FDA for Qtorin

Palvella Therapeutics (PVLA) announced that the company has submitted the first module of its rolling new drug application, or NDA, to the FDA seeking approval of Qtorin 3.9% rapamycin anhydrous…

4 weeks ago - TheFly

Palvella Therapeutics Submits First Module of Rolling New Drug Application to FDA for QTORIN™ Rapamycin for the Treatment of Microcystic Lymphatic Malformations

FDA's rolling review process is intended to facilitate expedited review, enabling FDA to begin evaluating completed modules of the NDA before the full application is submitted

4 weeks ago - GlobeNewsWire

FDA grants rolling review to Palvella Therapeutics Qtorin rapamycin

Palvella Therapeutics (PVLA) announced today that FDA has granted rolling review for the company’s new drug application, or NDA, for Qtorin rapamycin for the treatment of microcystic lymphatic malform...

5 weeks ago - TheFly

FDA Grants Rolling Review of Palvella's QTORIN™ Rapamycin NDA for Microcystic Lymphatic Malformations

FDA's rolling review process is intended to facilitate expedited review, enabling FDA to begin evaluating completed sections of the NDA before the full application is submitted

5 weeks ago - GlobeNewsWire

Palvella Therapeutics Transcript: AGM 2026

The meeting covered board elections, auditor ratification, executive compensation, and an equity plan amendment, all of which were approved by majority vote. No questions were submitted by stakeholders during the Q&A session.

6 weeks ago - Transcripts

Palvella Therapeutics Transcript: Goldman Sachs 47th Annual Global Healthcare Conference 2026

The company is advancing its QTORIN platform for rare skin diseases, highlighted by positive phase III results for QTORIN rapamycin in microcystic lymphatic malformations and a robust pipeline expansion. With $260 million in cash, experienced commercial leadership, and multiple upcoming clinical milestones, it is positioned for significant growth in multi-billion dollar orphan markets.

7 weeks ago - Transcripts

Palvella Therapeutics completes Qtorin pre-new drug application meeting with FDA

Palvella Therapeutics (PVLA) announced completion of its pre-new drug application meeting with FDA for Qtorin 3.9% rapamycin anhydrous gel in microcystic lymphatic malformations. The pre-NDA meeting a...

7 weeks ago - TheFly

Palvella Therapeutics Announces Completion of FDA Pre-NDA Meeting for QTORIN™ Rapamycin in Microcystic Lymphatic Malformations

Palvella remains on track to submit an NDA in the second half of 2026 Microcystic lymphatic malformations are serious, chronic, lifelong vascular malformations that can cause persistent leaking, bleed...

7 weeks ago - GlobeNewsWire

Palvella Therapeutics to Participate in the Goldman Sachs 47th Annual Global Healthcare Conference 2026

WAYNE, Pa., June 02, 2026 (GLOBE NEWSWIRE) -- Palvella Therapeutics, Inc. (Palvella or the “Company”) (Nasdaq: PVLA), a clinical-stage biopharmaceutical company focused on developing and commercializi...

2 months ago - GlobeNewsWire

Palvella Therapeutics issued patent by USPTO for Qtorin pitavastatin program

Palvella Therapeutics (PVLA) announced the issuance of U.S. Patent No. 12,636,273 by the United States Patent and Trademark Office. The issued patent, exclusively licensed by Palvella from Yale Univer...

2 months ago - TheFly

Palvella Therapeutics Strengthens QTORIN™ Pitavastatin Intellectual Property with Yale-Licensed U.S. Patent Providing Protection into 2043

Yale-licensed U.S. patent provides broad protection for topical mevalonate pathway inhibition in porokeratosis, including disseminated superficial actinic porokeratosis (DSAP)

2 months ago - GlobeNewsWire

Palvella Therapeutics Named Healthcare & Life Sciences Company of the Year at the Philadelphia Alliance for Capital and Technologies (PACT) Ecosystem Awards

WAYNE, Pa., May 21, 2026 (GLOBE NEWSWIRE) -- Palvella Therapeutics, Inc. (Palvella or “the Company”) (Nasdaq: PVLA), a clinical-stage biopharmaceutical company focused on developing and commercializin...

2 months ago - GlobeNewsWire

Palvella Therapeutics announces new data from SELVA, TOIVA studies

Palvella Therapeutics (PVLA) announced new clinical data from the Phase 3 SELVA and Phase 2 TOIVA studies were reported at the International Society for the Study of Vascular Anomalies World…

2 months ago - TheFly

Palvella Therapeutics Presents New SELVA and TOIVA Data at the 2026 International Society for the Study of Vascular Anomalies World Congress Supporting QTORIN™ Rapamycin as a Potential First-in-Disease Therapy for Multiple Serious, Rare Vascular Malformations

In SELVA Phase 3 study, 100% of participants (13/13) aged 6–11 years were rated as “Much Improved” (+2) or “Very Much Improved” (+3) on the Microcystic Lymphatic Malformation Investigator Global Asses...

2 months ago - GlobeNewsWire

Palvella Therapeutics announces new data from TOIVA trial of Qtorin

Palvella Therapeutics (PVLA) announced new data from the Phase 2 TOIVA trial of Qtorin rapamycin in patients with cutaneous venous malformations were presented at the 83rd Annual Meeting of the…

2 months ago - TheFly

Palvella Therapeutics Announces New Data from the Phase 2 TOIVA Trial of QTORIN™ Rapamycin in Cutaneous Venous Malformations Presented at the 83rd Annual Meeting of the Society for Investigative Dermatology

100% of patients with bleeding at baseline demonstrated a statistically significant improvement on the Cutaneous Venous Malformations Investigator Global Assessment Bleeding scale (cVM-IGA Bleeding) a...

2 months ago - GlobeNewsWire

Palvella Therapeutics Announces Uplisting to the Nasdaq Global Market

Uplisting reflects Palvella's continued progress advancing potential first-in-disease therapies for serious, rare skin diseases and vascular malformations

2 months ago - GlobeNewsWire

Palvella Therapeutics initiated with an Overweight at Stephens

Stephens initiated coverage of Palvella Therapeutics (PVLA) with an Overweight rating and $220 price target Palvella is a clinical-stage biopharmaceutical company leveraging its Qtorin platform to tar...

2 months ago - TheFly