HAELO: a Phase 3, Multinational, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of NTLA-2002 in Participants with Hereditary Angioedema (HAE)
Latest Information Update: 07 Mar 2025
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At a glance
- Drugs NTLA-2002 (Primary)
- Indications Hereditary angioedema
- Focus Registrational; Therapeutic Use
- Acronyms HAELO
- Sponsors Intellia Therapeutics
- 22 Jan 2025 According to an Intellia Therapeutics, the first patient has been dosed at USA location. And, expects to complete enrollment in the second half of 2025 and submit a biologics license application (BLA) in 2026 to support the Company's plans for a U.S. launch in 2027.
- 09 Jan 2025 According to an Intellia Therapeutics, first patient to be dosed in 1Q25 and completed enrollment in 2H 2025.
- 19 Dec 2024 Planned initiation date changed from 1 Oct 2024 to 1 Dec 2024.