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Vertex Receives the US FDA Approval for Journavx (Suzetrigine) to Treat Acute Pain

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Vertex Receives the US FDA Approval for Journavx (Suzetrigine) to Treat Acute Pain

Shots: 

  • The FDA has approved Journavx (50mg; BID) to treat moderate-to-severe acute pain in adults 
  • JOURNAVX is an oral, non-opioid pain signal inhibitor that selectively targets NaV1.8 relative to other NaV channels  
  • The company is also testing suzetrigine for peripheral neuropathic pain (PNP), with ongoing P-III trial for diabetic neuropathy and plans for lumbosacral radiculopathy studies, subject to regulatory discussions 

Ref: Vertex | Image: Vertex

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Dipanshu Dixit

A passionate content writer with expertise in delivering high-quality and engaging content, Dipanshu is a keen reader and a versatile writer. Dipanshu dedicatedly covers news ranging from biopharma, life sciences, biotech, and MedTech to diagnostics and animal health companies, FDA, EMA, and biosimilar approvals. He can be contacted at connect@pharmashots.com

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