Parkinson’s disease market will be boosted by new drug approvals

2 July 2015

The Parkinson’s disease treatment market value across the eight major countries of the USA, France, Germany, Italy, Spain, the UK, Japan, and Brazil will reach $4.7 billion by 2022, driven primarily by an aging population and increasing disease prevalence, new research shows.

According to research and consulting firm GlobalData’s latest report, most late-stage pipeline agents are set to meet the needs of advanced Parkinson’s disease patients, with three drugs expected to launch by 2022, namely Acorda Therapeutics’ (Nasdaq: ACOR) CVT-301, opicapone, from Portuguese drugmaker BIAL, and tozadenant from Biotie Therapies (Nasdaq OMX: BTH1V).

In a strong first-quarter for Parkinson’s disease treatment, Impax’ (Nasdaq: IPXL) Rytary (carbidopa and levodopa; IPX066) was approved by the US Food and Drug Administration in January 2015, while Newron Pharmaceutical’s (NWRN: SIX) Xadago (safinamide) was approved in Europe in February and accepted for a New Drug Application by the FDA in March. Additionally, AbbVie’s (NYSE: ABBV) Duopa (carbidopa and levodopa), which has been available for over 10 years in Europe, also gained US approval in Q1 2015.

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