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Pfizer’s Elranatamab Study: Continued Access for Multiple Myeloma Patients

Pfizer’s Elranatamab Study: Continued Access for Multiple Myeloma Patients

Pfizer Inc ((PFE)) announced an update on their ongoing clinical study.

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Pfizer Inc. is conducting an Elranatamab Post Trial Access Study for participants with Multiple Myeloma, officially titled ‘ELRANATAMAB POST TRIAL ACCESS: AN OPEN-LABEL, SINGLE-ARM STUDY FOR PARTICIPANTS WITH MULTIPLE MYELOMA CONTINUING FROM PFIZER-SPONSORED ELRANATAMAB CLINICAL STUDIES’. The study aims to provide continued access to elranatamab for patients who have shown clinical benefit in previous trials. This is significant as it supports ongoing treatment for patients with limited options.

The intervention being tested is Elranatamab, a drug designed as a heterodimeric humanized full-length bispecific IgG2 kappa antibody. It targets BCMA on Multiple Myeloma cells and CD3 on T cells, aiming to enhance the immune response against cancer cells.

The study is designed as an open-label, single-arm trial with no masking, focusing on treatment. All participants receive Elranatamab until disease progression, unacceptable toxicity, withdrawal of consent, study termination, or commercial availability of the drug in their country.

The study began on October 3, 2023, and is currently recruiting. The last update was submitted on July 28, 2025. These dates are crucial for tracking the study’s progress and understanding its timeline.

This update may positively influence Pfizer’s stock performance by demonstrating continued commitment to innovative cancer treatments. It may also impact investor sentiment favorably, especially in the context of competitive advancements in cancer therapies.

The study is ongoing, with further details available on the ClinicalTrials portal.

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