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Tavapadon, a drug being tested to treat early Parkinson's disease, has shown great promise in a Phase III trial by AbbVie, the pharmaceutical company announced this week. Parkinson’s disease ...
A small new trial published in the journal Nature Medicine describes what would be two firsts for Parkinson's disease, if they pan out: a diagnostic test and a potential immune-based treatment ...
On Thursday, the FDA approved AbbVie Inc’s (NYSE:ABBV) Vyalev (foscarbidopa and foslevodopa) as the first and only subcutaneous 24-hour infusion of levodopa-based therapy for motor fluctuations ...
In the management of Parkinson's disease, due to the chronic nature of Parkinson's disease (PD), a broad-based program is needed that includes patient and family education, support-group services, general wellness maintenance, exercise, and nutrition. At present, no cure for the disease is known, but medications or surgery can provide relief ...
In September 2014, the company acquired Civitas Therapeutics for US$525 million, gaining the Phase III Parkinson's drug, CVT-301, the migraine drug CVT-427 and rights to the ARCUS pulmonary delivery system. [9] [10] Th ARCUS technology allows for the administration of drugs by inhalation. The FDA-approved drug Inbrija (levodopa inhalation ...
The combination was refused approval by the US Food and Drug Administration (FDA) in 2023. [11] It was approved for medical use in Canada in May 2023, [ 4 ] in Australia in March 2024, [ 1 ] and in the United States in October 2024.
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