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

OverviewStructured DataIssuesContributors
Is a
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Clinical study
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Allocation Type
Randomized
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Participating Facility
Northwestern University
Northwestern University
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Arizona Research Center
Arizona Research Center
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Stanford University
Stanford University
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University of Utah
University of Utah
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Yale University
Yale University
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Health Conditions in Trial
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Pachyonychia congenita
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Intervention Model
Sequential Assignment
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Intervention Name
PTX-022
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Placebo
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Interventional Trial Phase
Phase 3
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Phase 2
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Interventional Trial Purpose
Treatment
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Intervention Type
Drug
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Last Updated
August 19, 2020
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Masked Party
Investigator
0
Participant
0
Masking Type
Double
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Primary Completion Date
2020
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Trial Recruitment Size
73
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Trial Sponsor
Palvella Therapeutics, Inc.
Palvella Therapeutics, Inc.
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Clinical Trial Start Date
April 1, 2019
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Study Completion Date
2020
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Clinical Trial Study Type
Interventional
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NCT Number
NCT03920228
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Official Name
A Multicenter, Four-Part, Phase 2/3 Study Evaluating the Safety and Efficacy of PTX-022 in the Treatment of Adults With Moderate to Severe Pachyonychia Congenita
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Official Website
clinicaltrials.gov/study...920228
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