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

PHASE3CompletedINTERVENTIONAL
Enrollment

87

Participants

Timeline

Start Date

November 29, 2021

Primary Completion Date

June 30, 2023

Study Completion Date

June 30, 2023

Conditions
Pachyonychia Congenita
Interventions
DRUG

QTORIN 3.9% rapamycin anhydrous gel

QTORIN 3.9% rapamycin anhydrous gel

DRUG

Vehicle

Matching vehicle (QTORIN anyhydrous gel)

Trial Locations (8)

32073

Park Avenue Dermatology, Orange Park

55432

Minnesota Clinical Study Center, Fridley

78759

DermResearch, Inc., Austin

84107

University of Utah, Murray

94304

Stanford University, Palo Alto

97239

Oregon Health and Sciences University, Portland

06519

Yale University, New Haven

E11FR

Royal London Hospital, London

Sponsors
All Listed Sponsors
lead

Palvella Therapeutics, Inc.

INDUSTRY