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A Study to Evaluate the Efficacy and Safety of AK139 in Patients With Prurigo Nodularis.
Sponsor: Akeso
Summary
This is a multicenter, randomized, double-blind, placebo-controlled phase II clinical study to evaluate the efficacy and safety of AK139 in the treatment of subjects with prurigo nodularis. The total duration of the study (including screening period, treatment period and follow-up period) planned for each subject is approximately 24 weeks.
Official title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of AK139 in Subjects With Prurigo Nodularis
Key Details
Gender
All
Age Range
18 Years - 75 Years
Study Type
INTERVENTIONAL
Enrollment
132
Start Date
2026-10
Completion Date
2027-09
Last Updated
2026-10-20
Healthy Volunteers
No
Conditions
Interventions
AK139
Biological: AK139 low dose
Placebo
Other: Placebo
AK139
Biological: AK139 high dose