Sanofi SA ((SNY)), Sanofi ((DE:SNW)), Sanofi ((SNYNF)) announced an update on their ongoing clinical study.
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Sanofi is conducting a Phase 2a clinical study titled A Parallel-group Treatment, Phase 2a, Multicenter, Randomized, Double-blind, Placebo-controlled Umbrella Study to Evaluate the Efficacy and Safety of Frexalimab, SAR442970, and Rilzabrutinib in Participants Aged 16 to 75 Years With Primary Focal Segmental Glomerulosclerosis (FSGS) or Minimal Change Disease (MCD). The study aims to assess the change in proteinuria and its impact on remission rates of nephrotic syndrome using frexalimab, SAR442970, or rilzabrutinib compared to a placebo in individuals with FSGS or MCD.
The interventions being tested include three drugs: frexalimab, SAR442970, and rilzabrutinib, each intended to treat primary FSGS or MCD by potentially reducing proteinuria and improving remission rates.
This interventional study is randomized with a parallel assignment model and quadruple masking, involving participants, care providers, investigators, and outcomes assessors. The primary purpose of the study is treatment-focused, aiming to evaluate the efficacy and safety of the interventions.
The study began on December 19, 2024, with primary completion expected in 2025. The last update was submitted on July 24, 2025. These dates are crucial as they mark the progress and timeline for potential results that could influence market dynamics.
The outcome of this study could significantly impact Sanofi’s stock performance and investor sentiment, especially if the results show promise in treating FSGS or MCD. This could position Sanofi favorably against competitors in the nephrology treatment market, potentially leading to increased investor interest and stock value.
The study is ongoing, with further details available on the ClinicalTrials portal.