Phase 2a Study to Assess the Efficacy,Safety and Tolerability of GIA632 in Adult Participants With Moderate to Severe Atopic Dermatitis
Purpose
The main purpose of this Ph2a study is to evaluate the preliminary efficacy, safety and tolerability of GIA632 when administered to adult participants with moderate to severe atopic dermatitis (AD).
Condition
- Atopic Dermatitis
Eligibility
- Eligible Ages
- Between 18 Years and 100 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Able and willing to sign the informed consent form - Patients with a diagnosis of atopic dermatitis and disease for at least 1 year - Moderate to severe atopic dermatitis
Exclusion Criteria
- Participants with a clinically significant medical condition or infectious disease (as specified in the protocol) - Participants with any clinically significant abnormal clinical laboratory tests, vital signs, physical examination or ECG - Participant with any other active inflammatory skin disease would interfere with the appropriate assessment of atopic dermatitis in the opinion of the investigator - Participants with any chronic, uncontrolled medical condition, which would put the participant at increased risk during the study (e.g., uncontrolled: diabetes, hypertension) - Participants with any clinically unstable disease states that would likely require systemic corticosteroids (e.g., uncontrolled asthma) - Women of childbearing potential unless they are using highly effective methods of contraception (failure rate < 1% per year) while taking study treatment. Other protocol-defined inclusion/exclusion criteria may apply.
Study Design
- Phase
- Phase 2
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel Assignment
- Primary Purpose
- Treatment
- Masking
- Double (Participant, Investigator)
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Experimental GIA632 |
Active treatment arm |
|
|
Placebo Comparator Placebo |
Placebo treatment arm |
|
Recruiting Locations
Ctr for Dermatology Clinical Res
Fremont 5350734, California 5332921 95438
Fremont 5350734, California 5332921 95438
Care Access Hoboken
Hoboken 5099133, New Jersey 5101760 07030
Hoboken 5099133, New Jersey 5101760 07030
More Details
- Status
- Recruiting
- Sponsor
- Novartis Pharmaceuticals
Detailed Description
This is a randomized, placebo-controlled, parallel-group, non-confirmatory, investigator and participant blinded study in adult participants with moderate to severe AD.