A Randomized, Double-blind, Multicenter, Placebo-controlled Phase 3 Study With Open-label Period to Evaluate the Efficacy and Safety of Inebilizumab in Adults With Myasthenia Gravis
Latest Information Update: 18 Mar 2025
At a glance
- Drugs Inebilizumab (Primary)
- Indications Myasthenia gravis
- Focus Registrational; Therapeutic Use
- Acronyms MINT
- Sponsors Viela Bio
Most Recent Events
- 13 Mar 2025 According to an Amgen media release, Findings will be presented as a late-breaking oral presentation during the American Academy of Neurology (AAN) Annual Meeting on April 8, 2025, in San Diego.
- 13 Mar 2025 Results presented in the Amgen Media Release.
- 04 Feb 2025 According to an Amgen media release, in January 2025, the FDA granted UPLIZNA Orphan Drug Designation for the treatment of generalized myasthenia gravis (gMG) based upon data from the Phase 3 MINT study. Regulatory filing activities are underway with submission anticipated to be complete in H1 2025.