Vertex’s Journavx Has Non-Opioid Advantage, But Faces Commercial Headwinds

The drug maker won US FDA approval for the pain reliever in moderate to severe acute pain, but it has plans to expand into chronic pain as well.

Stamp saying approved
(Shutterstock)

Vertex Pharmaceuticals’ Journavx (suzetrigine) has gained US Food and Drug Administration approval for acute pain, but the question now is how well it might fare commercially, with analysts forecasting some potential challenges.

The FDA approved Journavx on 30 January for moderate to severe acute pain in adults. Vertex called the drug the first and only non-opioid oral pain signal inhibitor and the first new class of pain drugs to win FDA approval in more than 20 years

Key Takeaways
  • The FDA approved Vertex’s Journavx for moderate to severe acute pain in adults, the first new class of pain medication in more than 20 years.
  • The company is giving the drug a wholesale acquisition cost of $15.50 per pill or $31 per day, but hopes that it’s not being an opioid will make up for the much higher price

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