On October 22, 2019, the biopharmaceutical company, Biogen, announced that they will be going to the FDA to seek approval for their Alzheimer’s disease drug candidate, aducanumab. If approved, this would be the first new drug for Alzheimer’s disease in 15 years and the first to attack, directly, the amyloid plaques, one of the hallmarks of Alzheimer’s disease.
On October 22, 2019, the biopharmaceutical company, Biogen, announced that they will be going to the FDA to seek approval for their Alzheimer’s disease drug candidate, aducanumab. If approved, this would be the first new drug for Alzheimer’s disease in 15 years and the first to attack, directly, the amyloid plaques, one of the hallmarks of Alzheimer’s disease.
This is a surprise because in March, Biogen announced that they were stopping the trials early due to a futility analysis. Now they say that further data and analysis show that they did achieve efficacy and will be taking their data to the FDA. We don’t know how long this process with take but hopefully in a year or two we will know if the drug will be approved.
Aducanumab is an injected drug and people will need to get shots every 2-3 weeks. It is also likely to be expensive but compared to the cost of care for Alzheimer’s patients, could still be economically beneficial. We hope, of course, if the FDA approves the drug, insurance companies will then cover it.
According to the Alzheimer’s Association Facts & Figures 2019, 5 Million people have Alzheimer’s today and because it is 12% of the total population, we consider this an epidemic. Now that many people with Down syndrome are living into their 60s, what we have learned is that 95% of the population with Down syndrome is likely to develop Alzheimer’s and, statistically, this represents a crisis. Yet, people with Down syndrome have not been included in many of these trials and not enough is known about the disease progression in Down syndrome.
LuMind IDSC Foundation is leading a funding effort to address this crisis through the Down Syndrome Clinical Trials Network (DS-CTN). Since DS-CTN launched in 2018, four sites have begun enrolling adults with Down syndrome in the Longitudinal Investigation For the Enhancement of Down Syndrome Research (LIFE-DSR) – an observational investigation with the goal to better understand the cognitive and behavioral changes along with the health issues found in adults with Down syndrome as they progress toward Alzheimer’s disease. There are also two assessment tools, specifically for people with Down syndrome, in development. LIFE-DSR is expected to be completed by 2021 and LuMind IDSC will continue to monitor the progress of promising drug candidates to make sure that people with Down syndrome are included in future trials.
Read more about aducanumab in the press release from Biogen.
Source: LuMind IDSC