A Study of KHK4827 in Patients With Systemic Sclerosis
NCT04368403 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 8
Last updated 2025-07-11
Summary
Exploratory evaluation of pharmacokinetics and safety of KHK4827 in subjects with systemic sclerosis
Conditions
Interventions
- DRUG
-
KHK4827
210 mg every 2 weeks (Q2W), subcutaneous (SC) injection
Sponsors & Collaborators
-
Kyowa Kirin Co., Ltd.
lead INDUSTRY
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 70 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-10-06
- Primary Completion
- 2019-01-31
- Completion
- 2025-03-31
Countries
- Japan
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