Clinical Trials - PVLA

NCT IDTitleStatusPhasesStart DateCompletion DatePrimary Completion Date
NCT06653842A Phase 2, Baseline-Controlled Study Evaluating the Safety and Efficacy of PTX-022 (Sirolimus) Topical Gel 3.9% in the Treatment of Cutaneous Venous MalformationsRECRUITINGPHASE22024-12-202026-032025-12
NCT06239480SELVA: A Phase 3 Study Evaluating QTORIN 3.9% Rapamycin Anhydrous Gel in the Treatment of Microcystic Lymphatic MalformationsRECRUITINGPHASE32024-07-312026-072026-01
NCT05643872A Study Evaluating the Safety and Pharmacokinetics of QTORIN Rapamycin 3.9% Anhydrous Gel in the Treatment of Adults With Pachyonychia CongenitaRECRUITINGPHASE32022-11-152023-112023-10
NCT05050149Study Evaluating the Safety and Efficacy of PTX-022 (QTORIN Sirolimus) in the Treatment of Microcystic Lymphatic MalformationsCOMPLETEDPHASE22022-01-132022-12-152022-11-15
NCT05180708A 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 CongenitaCOMPLETEDPHASE32021-11-292023-06-302023-06-30
NCT04893486CODY: 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 SyndromeCOMPLETEDPHASE22021-05-062023-03-132023-03-13
NCT04520750VALO-2: Study Evaluating the Safety and Efficacy of PTX022 in the Treatment of Adults With Pachyonychia CongenitaCOMPLETEDPHASE32020-09-012022-12-152021-06-30
NCT03920228Phase 2/3 Study Evaluating the Safety and Efficacy of PTX-022 in Treatment of Adults With Pachyonychia CongenitaCOMPLETEDPHASE2, PHASE32019-04-012020-10-192020-09-19