Pfizer Inc ((PFE)) announced an update on their ongoing clinical study.
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Study Overview: Pfizer Inc. is conducting a post-marketing surveillance study titled Korean Post-marketing Surveillance for Xeljanz® 5 mg Film-coated Tablets and Xeljanz® 1 mg/mL Oral Solution in Patients With Active pJIA and jPsA. The study aims to assess the safety and effectiveness of Xeljanz in treating Juvenile Idiopathic Arthritis (JIA) in routine clinical practice in Korea, focusing on patients aged 2 to less than 18 years.
Intervention/Treatment: The study tests Xeljanz, a JAK inhibitor, which is administered to JIA patients to evaluate its safety and effectiveness. Xeljanz is already approved for rheumatoid arthritis in Korea, and this study extends its evaluation to younger patients with JIA.
Study Design: This is a prospective observational study using a cohort model. The study does not involve random allocation or masking, as it observes the effects of Xeljanz in a real-world setting over a period of up to 44 weeks.
Study Timeline: The study began on April 12, 2024, with the latest update submitted on August 1, 2025. These dates are crucial for tracking the study’s progress and ensuring timely updates on its findings.
Market Implications: The study’s findings could significantly impact Pfizer’s stock performance by potentially expanding Xeljanz’s market to include younger patients with JIA. Positive results may enhance investor confidence and position Pfizer favorably against competitors in the arthritis treatment market.
The study is ongoing, and further details are available on the ClinicalTrials portal.