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Learn more about the latest happenings at Otsuka. Select to see US news or read our press releases. You can also stay up to date with our global news in the link below.
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Senior Director, External Communications,
Otsuka America Pharmaceutical, Inc
Otsuka Holdings Co., Ltd. has decided to donate 20 million yen (approximately USD 164,000) through the Japanese Red Cross Society for humanitarian assistance to people whose lives have been severely affected in Ukraine and who have been evacuated to surrounding countries.
In addition, Otsuka Holdings is providing support to patients and people involved in treatment through the provision of Otsuka products, including pharmaceuticals.
Otsuka and Lundbeck announce the U.S. Food and Drug Administration (FDA) has approved the supplemental new drug application (sNDA) of REXULTI® (brexpiprazole) for the treatment of schizophrenia in pediatric patients 13 to 17 years of age. The FDA previously granted Priority Review for the sNDA, a designation for a drug application that, if approved, would represent a significant improvement in the safety and/or effectiveness of the treatment, diagnosis, or prevention of a serious medical condition. REXULTI was approved in the U.S. in 2015 for the treatment of schizophrenia in adults and for adjunctive treatment of major depressive disorder in adults.
The McQuade Center for Strategic Research and Development, LLC, a member of the global Otsuka family of pharmaceutical companies, and Mindset Pharma Inc. announce a collaboration that will support the development of psychedelic medicines. MSRD has made a strategic investment to support the discovery and development of novel chemical entity assets of Mindset, a drug discovery and development company focused on creating optimized and patentable next-generation psychedelic medicines to treat neurological and psychiatric disorders with unmet medical needs.
Otsuka America Pharmaceutical, Inc. (OAPI), acknowledges the importance of the favorable opinion of Otsuka’s Hospital Free Trial Program by the Department of Health and Human Services (HHS) Office of Inspector General (OIG), which provides guidance for the design of manufacturer inpatient free trial programs that provide long-acting anti-psychotic injectable (LAI) products for the treatment of serious mental illness in a hospital setting.