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Not Yet RecruitingNCT06767540

A Clinical Study of AK120 in Adolescents With Moderate-to-severe Atopic Dermatitis

A Randomized Double-blind, Placebo-controlled, Multicenter Phase III Clinical Study Evaluating the Efficacy and Safety of AK120 in the Treatment of Moderate-to-severe Atopic Dermatitis (AD) in Adolescents

Status
Not Yet Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
198 (estimated)
Sponsor
Akeso · Industry
Sex
All
Age
12 Years – 18 Years
Healthy volunteers
Not accepted

Summary

This is a randomized double-blind, placebo-controlled, multicenter phase III clinical study evaluating the efficacy and safety of AK120 in the treatment of moderate-to-severe AD in adolescents.

Detailed description

This is a randomized double-blind, placebo-controlled, multicenter phase III clinical study to evaluate the safety and efficacy of AK120 in the treatment of moderate-to-severe AD in adolescents. The total duration of the study planned is approximately 57 weeks.

Conditions

Interventions

TypeNameDescription
DRUGPlaceboplacebo subcutaneous injection Q2W until week 46.
DRUGplaceboplacebo subcutaneous injection Q3W until week 45.

Timeline

Start date
2025-01-23
Primary completion
2027-07-10
Completion
2027-07-10
First posted
2025-01-10
Last updated
2025-01-10

Locations

28 sites across 1 country: China

Source: ClinicalTrials.gov record NCT06767540. Inclusion in this directory is not an endorsement.