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Otsuka and Lundbeck Announce U.S. Food and Drug Administration (FDA) Approval of Supplemental New Drug Application (sNDA) for REXULTI® (brexpiprazole) for the Treatment of Agitation Associated with Dementia Due to Alzheimer's Disease

REXULTI is the first and only pharmacological treatment approved in the U.S. for agitation associated with dementia due to Alzheimer’s diseasePRINCETON, N.J . ....

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Help on way for dementia patients? FDA green lights drug to treat agitation.

The supplemental approval was hailed as a “major milestone for patients, caregivers, and families.” ....

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Otsuka announces NICE recommendation of Lupkynis® (voclosporin) with mycophenolate mofetil for treating active lupus nephritis

Otsuka announces NICE recommendation of Lupkynis®      (voclosporin) with mycophenolate mofetil for treating active lupus nephritis LONDON, UK, 3 May 2023 – Otsuka Pharmaceuticals (U.K.) Ltd. announces that the National Institute for Health and C. ....

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FDA Approves Otsuka and Lundbeck's ABILIFY ASIMTUFII® (aripiprazole), the First Once-Every-Two-Months Long-acting Injectable (LAI) for the Treatment of Schizophrenia or Maintenance Monotherapy Treatment of Bipolar I Disorder in Adults | Illinois

PRINCETON, N.J. & DEERFIELD, Ill. (BUSINESS WIRE) Apr 27, 2023 ....

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Otsuka and Lundbeck Issue Statement on U.S. Food and Drug Administration (FDA) Advisory Committee Meeting on REXULTI® (brexpiprazole) for the Treatment of Agitation Associated with Alzheimer's Dementia | Illinois

PRINCETON, N.J. & DEERFIELD, Ill. (BUSINESS WIRE) Apr 16, 2023 ....

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