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Phase 1/2 Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of NTLA-2002 in Adults With Hereditary Angioedema (HAE)

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Trial Profile

Phase 1/2 Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of NTLA-2002 in Adults With Hereditary Angioedema (HAE)

Status: Active, no longer recruiting
Phase of Trial: Phase I/II

Latest Information Update: 26 Oct 2024

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At a glance

  • Drugs NTLA-2002 (Primary)
  • Indications Hereditary angioedema
  • Focus Adverse reactions; First in man; Proof of concept; Therapeutic Use
  • Sponsors Intellia Therapeutics

    • Most Recent Events

    • 24 Oct 2024 According to Intellia Therapeutics media release, Intellia will host a live webcast, on October 24, 2024, at 8:30 a.m. ET to discuss the NTLA-2002 Phase 2 data. The data cut-off date for the analysis was April 4, 2024, when the 25th patient completed the 16-week primary observation period.
    • 24 Oct 2024 Results presented in the Intellia Therapeutics Media Release
    • 24 Oct 2024 According to Intellia Therapeutics media release, Danny Cohn, M.D., Ph.D., Internist, Department of Vascular Medicine, Amsterdam University Medical Center, is the Lead Principal Investigator of the phase 2 part of this study.

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