Sanofi SA ((SNY)), Sanofi ((SNYNF)), Sanofi ((DE:SNW)) announced an update on their ongoing clinical study.
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Sanofi SA has launched a Phase 2 clinical study titled A Randomized, Phase 2, Open Label Study Evaluating Subcutaneous Administration of Isatuximab in Combination With Carfilzomib and Dexamethasone in Adult Participants With Relapsed and/or Refractory Multiple Myeloma (RRMM). The study aims to assess the efficacy of subcutaneous isatuximab combined with carfilzomib and dexamethasone in patients who have undergone 1 to 3 prior therapies. This study is significant as it explores a potentially more efficient delivery method for isatuximab, which could enhance treatment outcomes for RRMM patients.
The intervention being tested involves the subcutaneous administration of isatuximab, a monoclonal antibody, in combination with carfilzomib and dexamethasone. This combination is intended to improve the response rate in RRMM patients by targeting cancer cells more effectively.
The study employs a randomized, parallel assignment model without masking, focusing on treatment as its primary purpose. Participants are divided into cohorts to receive isatuximab either manually or via an On Body Delivery System (OBDS), with some switching between methods to evaluate efficacy and patient preference.
The study began on April 5, 2023, with an estimated completion date in July 2025. These timelines are crucial for tracking the progress and potential market introduction of the treatment, which could significantly impact Sanofi’s market position.
This clinical update could positively influence Sanofi’s stock performance by showcasing innovation in treatment delivery methods, potentially boosting investor confidence. As the pharmaceutical industry is highly competitive, advancements in drug administration could set Sanofi apart from its competitors.
The study is ongoing, and further details can be accessed on the ClinicalTrials portal.