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A Phase II, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of Nemolizumab in Patients with Acquired Reactive Perforating Collagenosis

Phase 2
Conditions
Acquired Reactive Perforating Collagenosis
Registration Number
JPRN-jRCT2021230034
Lead Sponsor
Tomoyuki Nishiura
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
21
Inclusion Criteria

Patients aged 18 years or older who have been diagnosed with acquired reactive perforating collagen fibrosis according to the diagnostic criteria of the Clinical Practice Guide for Perforated Dermatoses (2020)

Exclusion Criteria

Patients with immune deficiency
Patients with body weight less than 30.0kg
Patients with Hepatitis B virus or hepatitis C virus infection
Patients with Evidence of tuberculosis (TB) infection
Pregnant or lactating women.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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