NTLA-2002 in Adults With Hereditary Angioedema (HAE)

Last updated: March 23, 2026
Sponsor: Intellia Therapeutics
Overall Status: Active - Not Recruiting

Phase

1/2

Condition

Urticaria

Allergy

Allergies & Asthma

Treatment

Biological NTLA-2002

Normal Saline IV Administration

Clinical Study ID

NCT05120830
ITL-2002-CL-001
  • Ages > 18
  • All Genders

Study Summary

This study will be conducted to evaluate the safety, tolerability, activity, pharmacokinetics, and pharmacodynamics of NTLA-2002 in adults with Hereditary Angioedema (HAE).

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Age >18 years

  2. Diagnosis of HAE Types I or II

  3. Ability to provide evidence of HAE attacks to meet the screening requirement

  4. Subjects must have access to, and the ability to use, ≥ 1 acute medication(s) totreat angioedema attacks.

  5. Adequate chemistry and hematology measures at screening

  6. Subjects must agree not to participate in another interventional study for theduration of this trial.

  7. Subjects must be capable of providing signed informed consent

Exclusion

Exclusion Criteria:

  1. Concurrent diagnosis of any other type of recurrent angioedema

  2. Subjects who have known negative reaction or hypersensitivity to any lipidnanoparticles (LNP) component.

  3. Any condition that, in the Investigator's opinion, could adversely affect the safetyof the subject.

  4. Unwilling to comply with study procedures.

Study Design

Total Participants: 37
Treatment Group(s): 2
Primary Treatment: Biological NTLA-2002
Phase: 1/2
Study Start date:
December 10, 2021
Estimated Completion Date:
July 31, 2026

Connect with a study center

  • Clinical Trial Site

    Campbelltown,
    Australia

    Site Not Available

  • Clinical Trial Site

    Grenoble,
    France

    Site Not Available

  • Clinical Trial Site

    Lille,
    France

    Site Not Available

  • Clinical Trial Site

    Paris,
    France

    Site Not Available

  • Clinical Trial Site

    Berlin,
    Germany

    Site Not Available

  • Clinical Trial Site

    Frankfurt,
    Germany

    Site Not Available

  • Clinical Trial Site

    Amsterdam,
    Netherlands

    Site Not Available

  • Clinical Trial Site

    Auckland,
    New Zealand

    Site Not Available

  • Clinical Trial Site

    Cambridge,
    United Kingdom

    Site Not Available

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