Amlitelimab, an anti-OX40 ligand antibody, for atopic dermatitis: a plain language summary of STREAM-AD clinical study

Plain Language SummaryWhat is this summary about?This is a plain language summary of an article published in the Journal of Allergy and Clinical Immunology on November 8, 2024. The article described the results of the clinical study STREAM-AD. This study tested a medicine called amlitelimab in people with moderate-to-severe atopic dermatitis (AD, also called atopic eczema).AD is a common chronic skin disease that leads to severely itchy and dry skin. In AD, the immune system is overactive leading to chronic inflammation and damage to the skin. For some people with AD, medicated creams and ointments given by doctors do not work in reducing AD signs and symptoms.Amlitelimab is a new medicine given by injection under the skin that is being investigated and is not yet approved for use by the US Food and Drug Administration. Amlitelimab is an ‘anti-OX40 ligand antibody’, which means it is a medication that targets the OX40 ligand. This is a distinct part of the immune system not addressed by current therapies. The STREAM-AD clinical study looked at how well amlitelimab treatment worked in improving the signs and symptoms of AD. It also assessed how safe it was. All assessments involved comparing amlitelimab to placebo (dummy treatment) in people with AD for whom medicated creams and ointments did not work. The study also looked at how long relief from these signs and symptoms lasted after stopping treatment.What were the results?The study had two parts. Results from Part 1 showed that amlitelimab, given every 4 weeks, helped improve AD signs (e.g., extent and severity of red and dry skin) and symptoms (e.g., severity of itch) compared to placebo after 24 weeks.Participants who had skin that was clear or almost clear and/or experienced a 75% improvement in their Eczema Area and Severity Index (EASI) score after 24 weeks could begin Part 2 of the study. In Part 2, participants continued amlitelimab or stopped amlitelimab treatment for 28 weeks. Results from Part 2 showed that improvements seen in Part 1 were maintained regardless of whether participants continued taking amlitelimab or stopped. Amlitelimab was well tolerated, and the most commonly reported side effects were the common cold (known in the study as nasopharyngitis and upper respiratory tract infection), COVID-19 infection, and headache.What do the results mean?Amlitelimab, given every 4 weeks, improved AD signs and symptoms. Additionally, these effects of amlitelimab were maintained by most participants for 28 weeks after they stopped taking the medicine. This suggests the possibility of long-term relief. Amlitelimab was also shown to be well tolerated over 52 weeks.This is an abstract of the Plain Language Summary of Publication article.View the full Plain Language Summary PDF of this article to read the full-text

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