A US Food and Drug Administration advisory committee will discuss potential strategies for mitigating, monitoring and preventing various types of toxicities with adeno-associated virus (AAV) vector-based gene therapies at 2-3 September 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?