FDA approves self-administered autoinjector for UCB's myasthenia gravis drug Zilbrysq
Approval rests on bioequivalence and a 31-patient study with full dose delivery in 99.8% of injections; launch is expected in Q1 2027.
Approval rests on bioequivalence and a 31-patient study with full dose delivery in 99.8% of injections; launch is expected in Q1 2027.