A Study of TAK-279 in Adult Participants With Generalized Pustular Psoriasis or Erythrodermic Psoriasis
Launched by TAKEDA · Mar 15, 2024
Trial Information
Current as of August 31, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is testing a new treatment called TAK-279 for adults with two specific types of psoriasis: Generalized Pustular Psoriasis (GPP) and Erythrodermic Psoriasis (EP). The main goal is to see if TAK-279 can help improve the symptoms of these conditions and to monitor any side effects that participants might experience while using the treatment. If you have been diagnosed with GPP or EP and are considered a candidate for other therapies, you might be eligible to participate in this study.
Participants in the trial will receive TAK-279 and will be involved for up to 61 weeks, which includes 52 weeks of treatment. Throughout the study, participants will have multiple visits to the clinic for check-ups. It's important to know that this study is currently recruiting participants, and the eligibility criteria include having a confirmed diagnosis of GPP or EP, but not other types of psoriasis, and not having any recent infections or previous exposure to TAK-279. If you think you might qualify and are interested in helping advance psoriasis treatments, this study could be a good opportunity for you.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. A diagnosis of GPP or EP prior to the screening visit.
- • 2. Candidate for phototherapy or systemic therapy.
- Exclusion Criteria:
- • 1. Other forms of psoriasis.
- • 2. History of recent infection.
- • 3. Any prior exposure to TAK-279, or participation in any study that included a TYK2 inhibitor.
- • Other protocol defined inclusion/exclusion criteria apply.
About Takeda
Takeda Pharmaceutical Company Limited is a global, research-driven biopharmaceutical organization committed to advancing patient care through innovative therapies. Founded in 1781 and headquartered in Osaka, Japan, Takeda focuses on key therapeutic areas including oncology, gastroenterology, neuroscience, and rare diseases. With a strong emphasis on research and development, Takeda leverages cutting-edge science and technology to deliver transformative medicines that address unmet medical needs. The company is dedicated to sustainability and ethical practices, ensuring that its clinical trials uphold the highest standards of safety and efficacy while fostering collaboration with healthcare professionals and communities worldwide.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Kobe, Hyogo, Japan
Isehara, Kanagawa, Japan
Kobe, , Japan
Nagoya, Aichi, Japan
Okayama, , Japan
Fukuoka, , Japan
Itabashi Ku, Tokyo, Japan
Shinjuku Ku, Tokyo, Japan
Kyoto, , Japan
Minato Ku, Tokyo, Japan
Tsu, Mie, Japan
Kitakyushu, Fukuoka, Japan
Toyoake, Aichi, Japan
Hirakata, Osaka, Japan
Urayasu, Chiba, Japan
Osaka, , Japan
Kisarazu, Chiba, Japan
Isesaki, Gunma, Japan
Iruma, Saitama, Japan
Chuo City, Tokyo, Japan
Osaka, , Japan
Patients applied
Trial Officials
Study Director
Study Director
Takeda
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported