RecruitingNCT07132567
Assessment of Safety and Efficacy of Poteligeo Inj. 20 mg (Mogamulizumab) Through Use-result Surveillance
Sponsor
Kyowa Kirin Co., Ltd.
Enrollment
15 participants
Start Date
May 2, 2025
Study Type
OBSERVATIONAL
Conditions
Summary
The purpose of this surveillance is to assess the safety and efficacy of Poteligeo Inj. 20 mg (mogamulizumab) in routine clinical settings.
Eligibility
Min Age: 19 Years
Plain Language Summary
Simplified for easier understanding
This study is monitoring the real-world safety and effectiveness of a drug called mogamulizumab (brand name Poteligeo) in patients with two rare types of skin lymphoma: mycosis fungoides and Sézary syndrome. This is a post-approval safety monitoring study, not a randomized trial.
**You may be eligible if...**
- You are 19 or older
- You have been diagnosed with mycosis fungoides or Sézary syndrome (two types of cutaneous T-cell lymphoma, a rare skin cancer)
- You have already received at least one prior systemic therapy
- You are currently receiving or are being considered for mogamulizumab (Poteligeo) as part of your standard care
- You have given consent to have your personal health information used
**You may NOT be eligible if...**
- You have a known allergy to any ingredient in Poteligeo
- You intend to use this drug for a purpose outside its approved use
Talk to your doctor to see if this trial is right for you.
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Interventions
DRUGPoteligeo 20mg
Poteligeo 20mg
Locations(6)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07132567
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