Second Dupixent Phase 3 Trial Confirms Significant Improvements In Inflammatory Skin Disease

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Sanofi SA SNY and Regeneron Pharmaceuticals Inc REGN have announced data from the second Phase 3 trial of Dupixent (dupilumab) in adults with uncontrolled prurigo nodularis, a chronic type 2 inflammatory skin disease. 

  • The trial met its primary and key secondary endpoints, showing it significantly reduced itch and skin lesions compared to placebo at 24 weeks. 
  • The data confirm the positive results that were previously reported from the Phase 3 PRIME2 trial and will be submitted to regulatory authorities starting in 1H of 2022
  • In Phase 3 PRIME trial, topline results comparing Dupixent (n=75) to placebo (n=76) showed that more than three times as many Dupixent patients experienced a clinically meaningful reduction in itch from baseline (60% vs. 18%).
  • Nearly three times as many Dupixent patients achieved clear or almost clear skin, a secondary endpoint (48% vs. 18%). 
  • Overall rates of treatment-emergent adverse events were 71% for Dupixent and 63% for placebo. 
  • Price Action: SNY shares are down 0.69% at $51.81 during the premarket session on the last check Wednesday, and REGN stock closed at $611.22 on Tuesday.
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