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collections for the duration of the study\n\nParent Clinical Trial-Specific Criteria:\n\n* Study CS45570 participants who continued to be evaluated at the Week 36 follow up visit and achieved =\\> EASI50 response from study baseline\n\nExclusion Criteria:\n\n* Evidence of other skin conditions that would interfere with the assessment of AD\n* Withdrawal of consent and\u002For premature discontinuation from parent study\n* Any permanent discontinuation of study drug in parent study\n* History of severe allergic reaction or anaphylactic reaction to any biologic agent or known hypersensitivity to any component of Afimkibart","ALL","18 Years",{"count":389,"type":390},120,"ESTIMATED","INTERVENTIONAL",[393],"PHASE2","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.",[396],"Atopic 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