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Palvella Therapeutics, Inc.

Palvella Therapeutics, Inc. logo
🇺🇸United States
Ownership
Holding
Established
2015-01-01
Employees
1
Market Cap
-
Website
http://www.palvellatx.com

A Phase 2, Baseline-Controlled Study Evaluating the Safety and Efficacy of PTX-022 (Sirolimus) Topical Gel 3.9% in the Treatment of Cutaneous Venous Malformations

Phase 2
Recruiting
Conditions
Cutaneous Venous Malformations
Interventions
First Posted Date
2024-10-22
Last Posted Date
2025-03-28
Lead Sponsor
Palvella Therapeutics, Inc.
Target Recruit Count
15
Registration Number
NCT06653842
Locations
🇺🇸

Children's Hospital of Orange County, Irvine, California, United States

🇺🇸

Colorado Children's Hospital, Aurora, Colorado, United States

🇺🇸

John's Hopkins, Baltimore, Maryland, United States

and more 7 locations

SELVA: A Phase 3 Study Evaluating QTORIN 3.9% Rapamycin Anhydrous Gel in the Treatment of Microcystic Lymphatic Malformations

Phase 3
Recruiting
Conditions
Microcystic Lymphatic Malformation
Interventions
First Posted Date
2024-02-02
Last Posted Date
2025-04-01
Lead Sponsor
Palvella Therapeutics, Inc.
Target Recruit Count
40
Registration Number
NCT06239480
Locations
🇺🇸

Children's Hospital of Orange County, Irvine, California, United States

🇺🇸

University of Utah Health, Salt Lake City, Utah, United States

🇺🇸

Stanford University, Palo Alto, California, United States

and more 12 locations

A Study Evaluating the Safety and Pharmacokinetics of QTORIN Rapamycin 3.9% Anhydrous Gel in the Treatment of Adults With Pachyonychia Congenita

Phase 3
Recruiting
Conditions
Pachyonychia Congenita
Interventions
First Posted Date
2022-12-09
Last Posted Date
2022-12-09
Lead Sponsor
Palvella Therapeutics, Inc.
Target Recruit Count
45
Registration Number
NCT05643872
Locations
🇺🇸

Minnesota Clinical Study Center, New Brighton, Minnesota, United States

A Multicenter, Phase 3 Randomized, Double-Blind, Vehicle-Controlled Study Evaluating the Safety and Efficacy of QTORIN 3.9% Rapamycin Anhydrous Gel in the Treatment of Pachyonychia Congenita

Phase 3
Completed
Conditions
Pachyonychia Congenita
Interventions
First Posted Date
2022-01-06
Last Posted Date
2024-08-29
Lead Sponsor
Palvella Therapeutics, Inc.
Target Recruit Count
87
Registration Number
NCT05180708
Locations
🇺🇸

Oregon Health and Sciences University, Portland, Oregon, United States

🇺🇸

Stanford University, Palo Alto, California, United States

🇺🇸

Park Avenue Dermatology, Orange Park, Florida, United States

and more 5 locations

Study Evaluating the Safety and Efficacy of PTX-022 (QTORIN Sirolimus) in the Treatment of Microcystic Lymphatic Malformations

Phase 2
Completed
Conditions
Microcystic Lymphatic Malformation
Interventions
First Posted Date
2021-09-20
Last Posted Date
2025-01-17
Lead Sponsor
Palvella Therapeutics, Inc.
Target Recruit Count
12
Registration Number
NCT05050149
Locations
🇺🇸

Arkansas Children's Hospital, Little Rock, Arkansas, United States

🇺🇸

Children's Hospital of Pennsylvania (CHOP), Philadelphia, Pennsylvania, United States

🇺🇸

Minnesota Clinical Study Center, Fridley, Minnesota, United States

and more 4 locations

CODY: A Study Evaluating The Safety And Efficacy Of QTORIN 3.9% Sirolimus Topical Gel For The Prevention Of Basal Cell Carcinomas (BCCs) In Patients With Gorlin Syndrome

Phase 2
Completed
Conditions
BCCs in Gorlin Syndrome Patients
Interventions
Drug: Vehicle comparator
First Posted Date
2021-05-19
Last Posted Date
2024-08-29
Lead Sponsor
Palvella Therapeutics, Inc.
Target Recruit Count
73
Registration Number
NCT04893486
Locations
🇺🇸

DermResearch Inc, Austin, Texas, United States

🇺🇸

Mayo Clinic, Scottsdale, Arizona, United States

🇺🇸

Virginia Clinical Research, Inc., Norfolk, Virginia, United States

and more 13 locations

VALO-2: Study Evaluating the Safety and Efficacy of PTX022 in the Treatment of Adults With Pachyonychia Congenita

Phase 3
Completed
Conditions
Pachyonychia Congenita
Interventions
First Posted Date
2020-08-20
Last Posted Date
2024-08-29
Lead Sponsor
Palvella Therapeutics, Inc.
Target Recruit Count
36
Registration Number
NCT04520750
Locations
🇺🇸

Arizona Research Center, Phoenix, Arizona, United States

🇺🇸

Minnesota Clinical Study Center, Fridley, Minnesota, United States

🇺🇸

Stanford University, Palo Alto, California, United States

and more 1 locations

Phase 2/3 Study Evaluating the Safety and Efficacy of PTX-022 in Treatment of Adults With Pachyonychia Congenita

Phase 2
Completed
Conditions
Pachyonychia Congenita
Interventions
Drug: Placebo
First Posted Date
2019-04-18
Last Posted Date
2024-08-29
Lead Sponsor
Palvella Therapeutics, Inc.
Target Recruit Count
73
Registration Number
NCT03920228
Locations
🇺🇸

International Dermatology Research, Miami, Florida, United States

🇺🇸

Northwestern University, Chicago, Illinois, United States

🇺🇸

Arizona Research Center, Phoenix, Arizona, United States

and more 6 locations
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