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Lonvo-z

Research only

hereditary angioedema

Published evidence

2 publications2 exact-program0 related1 context / correction notes

Review publications

Program details

Sponsor filing describes an in vivo CRISPR therapy and a March 10, 2027 FDA target.

Program names
lonvoguran ziclumeran / lonvo-z / NTLA-2002
Modality
Gene editing
Indication
hereditary angioedema
Associated trial
NCT06634420
FDA target
March 10, 2027Date-only guidance; not a trading cutoff.

Publications 2

Evidence is grouped by its relationship to this program.

Search PubMed

Publication notes explain the evidence behind this program. PubMed / NCBI data notice

Coverage & interpretation
  • Primary HAELO phase 3 and earlier phase 2 papers match the HAE program; their cohorts and follow-up differ.

Exact program / indication

2 records
Exact programhuman clinicalPMID 42294842

Lonvoguran Ziclumeran - In Vivo CRISPR Gene Editing in Hereditary Angioedema.

The New England journal of medicine · 2026-06-13

In a randomized, placebo-controlled trial of 80 participants, a single lonvo-z infusion reduced HAE attack frequency during the prespecified follow-up window. The abstract reports infusion-related and other adverse events; it does not establish lifelong safety or an FDA outcome.

Program relevance

Phase 3 HAELO (NCT06634420) studies lonvo-z in hereditary angioedema, matching the catalog program.

Formulation / population: Single-dose intravenous lonvo-z in HAE with C1-inhibitor deficiency.

Journal Article / Randomized Controlled Trial / Clinical Trial, Phase III / Multicenter Study

Exact programhuman clinicalPMID 39445704

CRISPR-Based Therapy for Hereditary Angioedema.

The New England journal of medicine · 2024-10-24

A small randomized phase 2 study compared two single NTLA-2002 doses with placebo. Treated groups had fewer HAE attacks and reduced plasma kallikrein; the authors supported further phase 3 investigation.

Program relevance

Earlier NTLA-2002 phase 1/2 program (NCT05120830) in hereditary angioedema; this is not the later HAELO cohort.

Formulation / population: Single intravenous NTLA-2002 doses of 25 or 50 mg in adults with HAE.

  • Earlier phase 1/2 program; different cohort and follow-up from HAELO.

Clinical Trial, Phase II / Journal Article / Multicenter Study / Randomized Controlled Trial

Sources

Publication and retrieval dates are shown separately. Market rules determine which evidence can resolve an outcome.

sec-filingir.intelliatx.com
Sponsor filing describes an in vivo CRISPR therapy and a March 10, 2027 FDA target.
Published
Sep 8, 2026
Retrieved
2026-10-30 02:09:48 UTC
sponsor-clinical-trialswww.intelliatx.com
Sponsor clinical-trials page links HAELO to NCT06634420.
Published
Not supplied
Retrieved
2026-10-30 02:09:48 UTC
clinical-trial-registryclinicaltrials.gov
Registry identifies the associated compound, condition and sponsor; trial completion is separate from FDA action.
Published
Not supplied
Retrieved
2026-10-30 02:09:48 UTC

Research identity and publications do not establish regulatory approval, clinical suitability or an executable market. Read the limits