Pfizer Inc ((PFE)) announced an update on their ongoing clinical study.
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Study Overview: Pfizer Inc. has initiated a study titled Impact of Nirmatrelvir and Ritonavir (PAXLOVID®) on Mortality, Progression to Severe Disease, and Activities of Daily Living (ADL) Worsening in Long-term Care Hospitals (LTCHs) in Korea. The study aims to evaluate the effectiveness of Paxlovid in reducing severe illness, mortality, and daily activity decline in adults aged 60 and older residing in Korean long-term care hospitals who have contracted COVID-19.
Intervention/Treatment: The study focuses on the drug Paxlovid, a combination of Nirmatrelvir and Ritonavir, administered to participants as part of their routine COVID-19 care. The treatment is intended to mitigate severe disease outcomes and support daily functioning in older adults.
Study Design: This is an observational cohort study with a retrospective time perspective. Participants are divided into two groups: those treated with Paxlovid and those who were not. The study will compare health outcomes between these groups based on existing medical records.
Study Timeline: The study was first submitted on July 24, 2025, and is currently not yet recruiting participants. The timeline includes key milestones such as the start date and the last update, both crucial for tracking the study’s progress and potential impact.
Market Implications: This study could influence Pfizer’s stock performance by potentially validating Paxlovid’s effectiveness in a vulnerable population, thus enhancing investor confidence. The results may also affect the competitive landscape, as other pharmaceutical companies are developing similar COVID-19 treatments.
The study is ongoing, with further details available on the ClinicalTrials portal.