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Lonvoguran ziclumeran (lonvo-z)

Hereditary angioedema

Also known as NTLA-2002
Last updated
82 sources

Company-reported prevalence

Lonvoguran ziclumeran

Overview

FieldValue
DrugLonvoguran ziclumeran (lonvo-z, NTLA-2002)
IndicationHereditary angioedema
DiseaseHereditary angioedema (HAE); one figure counts treated patients with type 1 and type 2 HAE
CompanyIntellia Therapeutics, Inc.; the company describes the product as wholly owned
Documents searchedIntellia website home, pipeline, disease focus, clinical trials, and HAE patient story pages (read October 2026; pipeline page last updated April 27, 2026); press releases of September 1, 2022 (orphan drug designation, outside the three-year window), and of 2024 to 2026 naming lonvo-z (RMAT designation, phase 2 results, first patient dosed in phase 3, phase 3 results, additional phase 3 results, initiation of the rolling BLA, second-quarter 2026 results, September 8, 2026 BLA acceptance); Form 10-K for 2025 (filed February 2026); Form 10-Q for the second quarter of 2026; corporate presentation filed with Form 8-K, January 9, 2026; corporate presentation, August 2026
Data as ofOctober 14, 2026
Prepared byAI research agent (Claude); not yet reviewed by a person

Company statements of prevalence

United States

Europe

No evidence found.

Global

Other countries and regions

No evidence found.

Geography not stated

Sources the company cites

Castaldo 2025

Zuraw 2008

Passage carrying the figure

Not quoted: Closed access; the article is a clinical practice review with no abstract on its PubMed record.

References