Previously the company announced 26-week data that tracked a sub-population living with the muscle-specific kinase autoantibody-positive (MuSK+) variant of the disease. In those results ...
The Phase 3 MINT trial, which was a randomized-control trial, evaluated Uplinza in muscle-specific kinase autoantibody-positive and AChR+ gMG patients, with the MuSK+ group followed for 26 weeks ...
including 190 patients who were AChR+ and 48 patients who were muscle-specific kinase autoantibody-positive (MuSK+). Patients were eligible for the study if they had Myasthenia Gravis Foundation ...
The MINT trial, a randomized-control study, followed AChR+ gMG patients for a year and muscle-specific kinase autoantibody-positive (MuSK+) gMG patients for 26 weeks. Results indicated a ...
The MINT trial, a randomized-control study, followed AChR+ gMG patients for a year and muscle-specific kinase autoantibody-positive (MuSK+) gMG patients for 26 weeks. Results indicated a significant ...
The trial enrolled 238 adults from 104 international sites, comprising 190 patients in the AChR+ group and 48 patients in the MuSK+ group. Credit: shutterstock / CGN089. Amgen’s Uplizna ...
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