US Patents for PCT: WO2010/117937
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Patented / Exclusive Use |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Vanda Pharms Inc | BYSANTI | milsaperidone | TABLET;ORAL | 220358-001 | Feb 20, 2026 | RX | Yes | Yes | 9,074,255 | ⤷ Start Trial | METHOD FOR ACUTE TREATMENT OF MANIC OR MIXED EPISODES ASSOCIATED WITH BIPOLAR I DISORDER IN ADULTS BY ADMINISTERING MILSAPERIDONE TO A PATIENT BY LOWERING THE DOSE AFTER DETERMINING THAT THE PATIENT HAS A GENETIC PREDISPOSITION FOR QT PROLONGATION | ||||
| Vanda Pharms Inc | BYSANTI | milsaperidone | TABLET;ORAL | 220358-001 | Feb 20, 2026 | RX | Yes | Yes | 9,074,255 | ⤷ Start Trial | METHOD FOR TREATMENT OF SCHIZOPHRENIA IN ADULTS BY ADMINISTERING MILSAPERIDONE TO A PATIENT BY LOWERING THE DOSE AFTER DETERMINING THAT THE PATIENT HAS A GENETIC PREDISPOSITION FOR QT PROLONGATION | ||||
| Vanda Pharms Inc | BYSANTI | milsaperidone | TABLET;ORAL | 220358-002 | Feb 20, 2026 | RX | Yes | No | 9,074,255 | ⤷ Start Trial | METHOD FOR ACUTE TREATMENT OF MANIC OR MIXED EPISODES ASSOCIATED WITH BIPOLAR I DISORDER IN ADULTS BY ADMINISTERING MILSAPERIDONE TO A PATIENT BY LOWERING THE DOSE AFTER DETERMINING THAT THE PATIENT HAS A GENETIC PREDISPOSITION FOR QT PROLONGATION | ||||
| Vanda Pharms Inc | BYSANTI | milsaperidone | TABLET;ORAL | 220358-002 | Feb 20, 2026 | RX | Yes | No | 9,074,255 | ⤷ Start Trial | METHOD FOR TREATMENT OF SCHIZOPHRENIA IN ADULTS BY ADMINISTERING MILSAPERIDONE TO A PATIENT BY LOWERING THE DOSE AFTER DETERMINING THAT THE PATIENT HAS A GENETIC PREDISPOSITION FOR QT PROLONGATION | ||||
| Vanda Pharms Inc | BYSANTI | milsaperidone | TABLET;ORAL | 220358-003 | Feb 20, 2026 | RX | Yes | No | 9,074,255 | ⤷ Start Trial | METHOD FOR ACUTE TREATMENT OF MANIC OR MIXED EPISODES ASSOCIATED WITH BIPOLAR I DISORDER IN ADULTS BY ADMINISTERING MILSAPERIDONE TO A PATIENT BY LOWERING THE DOSE AFTER DETERMINING THAT THE PATIENT HAS A GENETIC PREDISPOSITION FOR QT PROLONGATION | ||||
| >Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >TE | >Type | >RLD | >RS | >Patent No. | >Patent Expiration | >Product | >Substance | >Delist Req. | >Patented / Exclusive Use |
