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The FDA approved BYSANTI, a new antipsychotic for bipolar mania and schizophrenia, with a U.S. launch expected in Q3 2026.
The FDA has approved BYSANTI (milsaperidone), a new atypical antipsychotic, for acute treatment of manic or mixed episodes in adults with Bipolar I Disorder and for schizophrenia.
Developed by Vanda Pharmaceuticals, it is a first new chemical entity with a well-established safety profile based on real-world use of its active metabolite, iloperidone.
The drug is expected to launch in the U.S. third quarter of 2026 and is protected by patents and data exclusivity through 2044.
It is also being studied as a treatment for treatment-resistant depression, with results expected by end of 2026.
The approval follows Vanda’s earlier FDA nod for NEREUS in December 2025.
La FDA aprobó BYSANTI, un nuevo antipsicótico para la manía bipolar y la esquizofrenia, con un lanzamiento en EE. UU. previsto para el tercer trimestre de 2026.