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VALO-2: Study Evaluating the Safety and Efficacy of PTX022 in the Treatment of Adults With Pachyonychia Congenita
Condition: Pachyonychia Congenita · Sponsor: Palvella Therapeutics, Inc.
About this study
VALO-2 is a multicenter, open-label extension (OLE) study enrolling patients with genotyped keratin mutations KRT6A, KRT6B and KRT16 who were previously treated with investigational PTX-022 during the VALO study. The purpose of the OLE study is to investigate long term exposure to investigational PTX-022 and evaluate safety and efficacy data. A sub-study is included to evaluate safety and efficacy of patients with genotyped keratin mutations of KRT6C and KRT17 not previously treated with investigational PTX-022.
This description comes directly from the study's public registry record.
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No contact information is available for this study as per the public registry record.
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Locations (4)
| Arizona Research Center | Phoenix, Arizona, United States | — |
| Stanford University | Palo Alto, California, United States | — |
| Minnesota Clinical Study Center | Fridley, Minnesota, United States | — |
| University of Utah | Murray, Utah, United States | — |
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Source record: clinicaltrials.gov/study/NCT04520750