Merck & Co. is awaiting regulatory approvals for its subcutaneous version of PD-1 inhibitor pembrolizumab, and its successful head-to-head trial against the original intravenous Keytruda (pembrolizumab) quantifies the convenience advantages. But while that may help to mitigate anticipated price controls under the Inflation Reduction Act, biosimilars of Keytruda will likely still present strong competition.
Key Takeaways
- Merck presented positive noninferiority data for its subcutaneous version of pembrolizumab versus intravenous Keytruda at the European Lung Cancer Conference, with the FDA expected to...
The drug maker presented data on 27 March at the European Lung Cancer Conference in Paris from the pivotal Phase III 3475A-D77 trial of subcutaneous pembrolizumab (MK-3475A), which combines the...
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on Scrip 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?