An Efficacy and Safety Study of RPT193 in Adults With Atopic Dermatitis
About the study
Phase 2 study of RPT193 in adults with atopic dermatitis
Who can take part
You may be eligible to participate in the study if you meet the following criteria:
INCLUSION CRITERIA
Inclusion Criteria:
- Clinically confirmed diagnosis of active atopic dermatitis (AD), according to the revised Hanifin and Rajka criteria
- 12-month history of AD and had no significant flares in AD for at least 4 weeks before screening
- inadequate response to a ≥1 month treatment with topical medications
- Atopic dermatitis covering ≥10% of the body surface area
- EASI score ≥16
- Validated Investigator Global Assessment (VIGA) ≥3
- Use of emollient(s) at least 2x daily for 1 week prior to baseline
- Negative coronavirus disease (COVID)-19 results at screening
EXCLUSION CRITERIA
Exclusion Criteria:
- Uncontrolled moderate-to-severe asthma
- Uncontrolled diabetes
- Stage III or IV cardiac failure
- Severe renal condition
- Major surgery within 8 weeks of screening
- Immunodeficiency and/or receipt of immunosuppressive drugs within 4 weeks of baseline
- Use of systemic Janus kinase (JAK) inhibitor within 8 weeks of baseline
- Received live or live-attenuated vaccine within 4 weeks of baseline
- Prior receipt of RPT193
Study Locations
Enter your ZIP code/Postal code/PIN code to locate study sites near you:
How to Apply
Contact the study center to learn if this study is a good match for you.
Study’s details
Contition
Atopic Dermatitis
Age (in years)
18 - 75
Phase
Phase 2
Participants needed
268
Est. Completion Date
Sep 30, 2024
Treatment type
Interventional
Sponsor
RAPT Therapeutics, Inc.
ClinicalTrials.gov identifier
NCT05399368
Study number
RPT193-02
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