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INTELLIA THERAPEUTICS INC · Data as of 2026-09-08
Upcoming catalysts
lonvoguran ziclumeran (also referred to as NTLA-2002) — Filing acceptance
H2 2026
Intellia expects the U.S. Food and Drug Administration (FDA) to accept its submission of a biologics license application (BLA) for lonvo-z in the second half of 2026.
Source filinglonvo-z — NDA/BLA submission
H1 2027
Rolling biologics license application (BLA) submission initiated with the U.S. Food and Drug Administration (FDA); anticipate U.S. launch in the first half of 2027, if approved
Source filinglonvoguran ziclumeran (also referred to as NTLA-2002) — Regulatory decision
H1 2027
The company continues to anticipate regulatory approval and a U.S. launch in the first half of 2027.
Source filingnexiguran ziclumeran (also referred to as NTLA-2001) — NDA/BLA submission
by 2028
Intellia anticipates submitting a biologics license application (BLA) for ATTRv-PN by 2028.
Source filingExplore the free biotech catalyst calendar