Atopic Dermatitis
Conditions
Brief summary
This is a multicenter, randomized, open label phase II clinical study to evaluate the safety and efficacy of AK120 in the treatment of subjects with moderate to severe atopic dermatitis.
Detailed description
This is a multicenter, randomized, open label phase II clinical study to evaluate the safety and efficacy of AK120 in the treatment of subjects with moderate to severe atopic dermatitis. The total duration of the study (including screening period) planned for each subject is approximately 29 weeks.
Interventions
DRUGAK120
subcutaneous injection every 2 weeks
Sponsors
Akeso
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
1. Male or female subjects aged ≥18≤75 years old. 2. Atopic dermatitis (AD) diagnosed at least half a year before screening. 3. Subject with EASI score ≥16, IGA ≥ 3, BSA ≥ 10% at screening and baseline. 4. Subjects with a history of an inadequate response or medically inappropriate use of topical drug treatment within 6 months
Exclusion criteria
1. Received systemic corticosteroids, immunosuppressive/immunomodulatory drugs, phototherapy within the 4 weeks before randomization. 2. Received systemic traditional Chinese medicine treatment within the 4 weeks before randomization or topical traditional Chinese medicine treatment within 1 week before randomization 3. Received treatment with other clinical study drugs within 1 month or 5 half-lives before randomization (whichever is longer) 4. Received or planned to receive live vaccine treatment within the 3 months before randomization or during the study period. 5. Received allergen specific immunotherapy within the 3 months before randomization. 6. Have a history of allergies to any component of AK120 and/or severe allergic reactions to monoclonal antibodies.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Incidence of adverse events(AE) | week 0 to week 24 | An AE is defined as any untoward medical occurrence in a participant administered a pharmaceutical product temporally associated with the use of study treatment, whether or not considered related to the study treatment |
Secondary
| Measure | Time frame |
|---|---|
| Percentage of subjects who achieved (Eczema Area and Severity Index) EASI-50 | at week 2/4/8/12/16 /20 and 24 |
| Percentage change in (Eczema Area and Severity Index) EASI scores from baseline | at week 2/4/8/12/16 /20 and 24 |
| Percentage of subjects who achieved (Eczema Area and Severity Index) EASI-75 | at week 2/4/8/12/16 /20 and 24 |
| Percentage of subjects with a (Investigator's Global Assessment) IGA score decrease of ≥ 2 points from baseline | at week 2/4/8/12/16 /20 and 24 |
| Percentage change in (affected body surface area) BSA score from baseline | at week 2/4/8/12/16 /20 and 24 |
| Percentage of subjects who achieved 0/1 in the (Investigator's Global Assessment) IGA | at week 2/4/8/12/16 /20 and 24 |
Countries
China
Outcome results
None listed