Pfizer Inc ((PFE)) announced an update on their ongoing clinical study.
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Pfizer Inc. is conducting an open-label extension study titled AN OPEN-LABEL EXTENSION STUDY TO EVALUATE THE LONG-TERM SAFETY, TOLERABILITY, AND EFFICACY OF MARSTACIMAB PROPHYLAXIS IN SEVERE (COAGULATION FACTOR ACTIVITY <1%) HEMOPHILIA A PARTICIPANTS WITH OR WITHOUT INHIBITORS OR MODERATELY SEVERE TO SEVERE HEMOPHILIA B PARTICIPANTS (COAGULATION FACTOR ACTIVITY ≤2%) WITH OR WITHOUT INHIBITORS. The study aims to evaluate the long-term safety, tolerability, and efficacy of marstacimab prophylaxis in participants with severe hemophilia A or B, with or without inhibitors. This research is significant as it addresses a critical need for effective long-term treatment options for hemophilia patients.
The intervention being tested is a drug named PF-06741086, also known as marstacimab. It is administered as a subcutaneous injection and is intended to serve as a prophylactic treatment to prevent bleeding episodes in hemophilia patients.
The study is designed as an interventional, single-group assignment with no masking, focusing on treatment as its primary purpose. Participants are allocated to receive the drug without a comparison group, allowing researchers to observe the effects of marstacimab directly.
The study began on November 11, 2021, and is currently recruiting participants. The primary completion date is yet to be determined, with the last update submitted on December 19, 2024. These dates are crucial for tracking the progress and availability of results.
This study update could positively impact Pfizer’s stock performance by demonstrating the company’s commitment to advancing hemophilia treatment. Positive results may enhance investor confidence and position Pfizer favorably against competitors in the hemophilia treatment market.
The study is ongoing, and further details are available on the ClinicalTrials portal.