AMAG Pharmaceuticals Inc. is open to conducting another randomized, controlled trial for Makena (hydroxyprogesterone caproate injection, also known as 17P), but the company also appears ready to challenge any effort by the US Food and Drug Administration to withdraw the preterm birth drug’s accelerated approval in the interim.
During a third quarter earnings call on 1 November, company executives addressed analyst questions about the FDA advisory committee meeting...
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on Pink Sheet for daily insights
- Start your 7-day free trial
- Explore trusted news, analysis, and insights
- Access comprehensive global coverage
- Enjoy instant access – no credit card required
Already a subscriber?