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A Phase 3, Open-Label, Multicenter Study to Evaluate the Efficacy, Safety, and Tolerability of TAK-279 in Adult Subjects With Generalized Pustular Psoriasis or Erythrodermic Psoriasis
The main aim of this study is to check if TAK-279 improves symptoms of With Generalized Pustular Psoriasis (GPP) or Erythrodermic Psoriasis (EP) and side effect from the study treatment or TAK-279. All participants will be assigned to study treatments of TAK-279 and will be treated with TAK-279 if the participants meet the study rules. Participants will be in the study for up to 61 weeks including 52 weeks of study treatment. During the study, participants will visit their study clinic for multiple times.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Nagoya City University Hospital
Nagoya, Aichi-ken, Japan
Fujita Health University Hospital
Toyoake, Aichi-ken, Japan
Kimitsu Chuo Hospital
Kisarazu, Chiba, Japan
Juntendo University Urayasu Hospital
Urayasu, Chiba, Japan
Hospital of the University of Occupational and Environmental Health, Japan
Kitakyushu, Fukuoka, Japan
Isesaki Municipal Hospital
Isesaki, Gunma, Japan
Kobe University Hospital
Kobe, Hyōgo, Japan
Tokai University Hospital
Isehara, Kanagawa, Japan
Mie University Hospital
Tsu, Mie-ken, Japan
Kansai Medical University Hospital
Hirakata, Osaka, Japan
Start Date
March 19, 2024
Primary Completion Date
October 15, 2025
Completion Date
July 22, 2026
Last Updated
November 17, 2025
18
ACTUAL participants
TAK-279
DRUG
Lead Sponsor
Takeda
NCT06477536
NCT07448428
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06886009