A pivotal, single, global, Phase 3 study evaluating the 240 mg dose of alvelestat versus placebo in patients with alpha-1-antitrypsin deficiency-associated lung disease (AATD-LD)
Latest Information Update: 19 Nov 2024
At a glance
- Drugs Alvelestat (Primary)
- Indications Alpha 1-antitrypsin deficiency
- Focus Registrational; Therapeutic Use
- Sponsors Mereo BioPharma
- 12 Nov 2024 According to a Mereo Biopharma media release, following the FDA feedback on the detailed Phase 3 package, including the study protocol and the initial validation work on SGRQ in AATD, the Company continues to expect that alvelestat will be Phase 3 ready around the end of 2024. Company remains in discussions with several potential partners regarding the development and commercialization of alvelestat for AATD.
- 13 Aug 2024 According to a Mereo Biopharma media release, At the end of Q2, Mereo submitted the initial validation work for SGRQ in AATD and the detailed Phase 3 package including the study protocol to the FDA.
- 27 Mar 2024 According to a Mereo Biopharma media release, The company aims to initiate the Phase 3 study with a partner around the end of 2024.