Study of the Efficacy, Safety, Pharmacokinetics, and Immunogenicity of Netakimab in Children With Moderate to Severe Plaque Psoriasis
NCT06640517 · Status: ACTIVE_NOT_RECRUITING · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 140
Last updated 2025-06-24
Summary
The aim of the study is to evaluate the efficacy and safety of netakimab compared with placebo in a pediatric population of subjects over 6 years of age with moderate to severe plaque psoriasis. The study will have randomized, double-blind, placebo-controlled study with open-arm comparison.
Conditions
Interventions
- DRUG
-
Netakimab
netakimab will be administered subcutaneously with induction once a week for the first three weeks, then once every 4 weeks
- DRUG
-
placebo will be administered subcutaneously at a scheme masking netakimab treatment
- DRUG
-
adalimumab will be administered subcutaneously at weeks 1, 2, and then once every 2 weeks
Sponsors & Collaborators
-
Biocad
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- QUADRUPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 6 Years
- Max Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-08-08
- Primary Completion
- 2026-06-30
- Completion
- 2028-02-29
Countries
- Russia
Study Locations
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