Intellia starts rolling FDA BLA submission for lonvo-z in hereditary angioedema
PUBT · 1h ago
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- Intellia began rolling BLA submission to FDA seeking approval of lonvoguran ziclumeran (lonvo-z) as one-time treatment for hereditary angioedema.
- Phase 3 HAELO trial hit primary, key secondary endpoints, showing most patients were free of attacks and ongoing therapy over six-month observation period.
- Company expects to complete BLA in second half of 2026; commercial launch targeted for first half of 2027 if cleared.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Intellia Therapeutics Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 202604270700PRIMZONEFULLFEED9707208) on April 27, 2026, and is solely responsible for the information contained therein.
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