Abbvie ((ABBV)), Abbvie (($CC:ABBV.CUR)) announced an update on their ongoing clinical study.
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AbbVie is conducting a Phase 3 clinical study titled ‘A Phase 3, Open-label, Efficacy-Assessor-Blinded Study, Comparing the Safety and Efficacy of Upadacitinib to Dupilumab in Children From 2 to Less Than 12 Years of Age With Moderate to Severe Atopic Dermatitis.’ The study aims to evaluate the safety and efficacy of oral Upadacitinib compared to subcutaneous Dupilumab in young children with moderate to severe atopic dermatitis, a condition characterized by skin inflammation, rash, and itching.
The interventions being tested are Upadacitinib, an oral tablet or solution, and Dupilumab, a subcutaneous injection. Upadacitinib is already approved for patients aged 12 and above, and this study seeks to expand its use to younger children. The objective is to assess adverse events and changes in disease activity.
The study is designed as a randomized, parallel-assignment trial with a single-blind masking for outcome assessors. Its primary purpose is treatment-focused, involving approximately 675 participants across 150 global sites. Participants are stratified by disease severity, age, and previous treatment response.
The study began on August 19, 2024, with an estimated primary completion date yet to be announced. The latest update was submitted on July 21, 2025. These dates are crucial as they indicate the study’s progress and potential timelines for results.
This study could significantly impact AbbVie’s stock performance and investor sentiment, as successful results may lead to expanded use of Upadacitinib in a younger demographic. This could enhance AbbVie’s competitive position in the dermatology market, especially against other companies offering treatments for atopic dermatitis.
The study is ongoing, with further details available on the ClinicalTrials portal.