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The global Alzheimer’s drugs market is expected to be driven by ageing global population and need for effective solutions to manage Alzheimer’s. It is reported that the number of cases of Alzheimer’s would nearly triple to 152.8 million by 2050. The prevalence of dementia across the world is reported to be as high as almost twenty-four million, and is projected to double every twenty years by 2040. As the global population continues to age, the number of individuals at risk are also expected to increase, especially among the very old. Significant regions include UAE, Qatar, USA, China, Germany, France, UK and Switzerland.
Alzheimer’s leads to problems with memory, thinking and behaviour. The disease worsens with time. While symptoms may widely vary, the symptoms that people first experience include forgetfulness severe enough to affect the ability to properly function at home or at work. Because of the disease, the sufferer may get confused, lost in familiar places, misplace things or experience trouble with language.
In 2021, it was reported that artificial intelligence revealed that current drugs could help combat Alzheimer’s Disease. A team at Massachusetts General Hospital (MGH) and Harvard Medical School (HMS) developed an artificial intelligence–based method to screen presently available medicines as probable treatments for Alzheimer’s Disease. The method could offer a quick and cost-effective way to repurpose existing therapies into new treatments for this progressive, debilitating neurodegenerative condition. Such developments are expected to drive the global Alzheimer’s drugs market. It could also help unveil novel, unexplored targets for therapy by indicating mechanisms of drug action.
In 2021, the U.S. Food and Drug Administration approved Aduhelm (aducanumab) for the treatment of Alzheimer’s. Aduhelm was approved using the accelerated approval pathway, which could be used for a drug for a range of life-threatening illness that offers a meaningful therapeutic advantage over existing treatments.
In 2021, The U.S. Food and Drug Administration (FDA) granted Breakthrough Therapy designation for donanemab, Eli Lilly and Company's investigational antibody therapy for Alzheimer's Disease (AD). The Breakthrough Therapy designation sought to expedite the development and review of drugs intended to treat a serious condition when preliminary clinical evidence indicated that the drug could exbibit considerable improvement on a clinically significant endpoint(s) over existing therapies with full FDA approval.
In 2021, Genentech’s Anti-Amyloid Beta Antibody Gantenerumab was granted FDA Breakthrough Therapy Designation in Alzheimer’s Disease. Gantenerumab was an investigational antibody in Phase III development for early Alzheimer's disease (AD). Gantenerumab was the first and only anti-amyloid antibody being examined for subcutaneous administration in late-stage trials for the treatment of Alzheimer’s Disease.
Key Findings of the Report:
Market Analysis by Drug Class, Distribution Channel and Region:
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