The University of Tokyo Hospital
Bunkyo-ku, Tokyo, 113-8655, Japan
NCT Number: NCT04368403
Exploratory evaluation of pharmacokinetics and safety of KHK4827 in subjects with systemic sclerosis
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Notify Me18 year–70 year
All sexes
Interventional
Phase 1
Bunkyo-ku, Tokyo, 113-8655, Japan
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
210 mg every 2 weeks (Q2W), subcutaneous (SC) injection
Time frame: Pre-dose, Week 1, 2, 4, 8, 12, 16, 22, 24, 36, 48, 52 and every 24 weeks through study completion until 2025.
Time frame: Pre-dose, Week 1, 2, 4, 8, 12, 16, 20, 24, 28, 32, 36, 40, 44, 48, 52 and every 8 weeks through study completion until 2025.
mRSS: scored 0(normal), 1(mild), 2(moderate), or 3(severe) per each site, assessed in 17 different body sites, total score=51
Kyowa Kirin Co., Ltd.
Industry
A Phase 1, Open-label, Multiple-dose Study of KHK4827 in Subjects With Systemic Sclerosis
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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