RecruitingAtopic Dermatitis
A Long Term Extension Study to Evaluate the Safety and Efficacy of Afimkibart (RO7790121) in Participants With Atopic Dermatitis
Eligible age
18+ yrs
Accepts
All genders
Locations
3 states
Healthy volunteers
No
See if you qualify for this study
Answer a few quick questions about your location and health. Takes about a minute.
About this study
This study will assess long-term safety and efficacy of Afimkibart (also known as RO7790121) in participants with Atopic Dermatitis (AD) who participated in previous afimkibart clinical trials.
Sponsor: Hoffmann-La Roche
You may qualify if…
- ✓ Ability and willingness to comply with all aspects of the protocol including completion of the efficacy assessments (EASI and IGA), clinical outcome assessment instruments (DLQI, POEM), and safety and PK sample collections for the duration of the study
- ✓ Parent Clinical Trial-Specific Criteria:
- ✓ Study CS45570 participants who continued to be evaluated at the Week 36 follow up visit and achieved =\> EASI50 response from study baseline
You may not qualify if…
- ✕ Evidence of other skin conditions that would interfere with the assessment of AD
- ✕ Withdrawal of consent and/or premature discontinuation from parent study
- ✕ Any permanent discontinuation of study drug in parent study
- ✕ History of severe allergic reaction or anaphylactic reaction to any biologic agent or known hypersensitivity to any component of Afimkibart
Where it's recruiting
Source: ClinicalTrials.gov · NCT07223697 · last updated 2026-06-09