FDA Accepts & Gives Priority Review to Intellia's BLA for HAE Drug
The FDA has accepted Intellia's Biologics License Application (BLA) for its hereditary angioedema (HAE) drug, lonvo-z, and granted it Priority Review. A regulatory decision is expected by March 10, 2027.
Why it matters — Priority Review signals faster regulatory evaluation of Intellia's HAE candidate, bringing the company closer to a potential approval decision.