Pfizer Inc ((PFE)) announced an update on their ongoing clinical study.
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Pfizer Inc. is conducting a clinical study titled ‘A Prospective, Single-arm, Open-label, Non-interventional, Multi-centre, Post Marketing Surveillance (PMS) Study of Mylotarg®.’ The study aims to evaluate the safety and effects of Mylotarg in treating acute myeloid leukemia (AML), a condition affecting white blood cells. The study is significant as it seeks to provide insights into the safety profile of Mylotarg, potentially influencing its use in AML treatment.
The intervention being tested is Mylotarg, a medication intended for the treatment of AML. The study focuses on the safety and efficacy of this drug in real-world settings, monitoring participants for adverse reactions and disease progression.
This observational study follows a cohort model with a prospective time perspective. It is designed to gather data on the effects of Mylotarg without any specific allocation or masking, focusing on understanding its impact in a naturalistic setting.
The study began on December 12, 2021, with the last update submitted on June 27, 2025. These dates are crucial as they mark the phases of data collection and analysis, with the study currently in the recruiting phase.
The update on this study could influence Pfizer’s stock performance and investor sentiment, as positive results may enhance Mylotarg’s market position. In the competitive landscape of AML treatments, advancements in safety and efficacy data can provide Pfizer with a strategic advantage.
The study is ongoing, with further details available on the ClinicalTrials portal.