The company said it will soon be seeking regulatory approval in the United States for the drug, called aducanumab, and it could be available within two years.
In a statement on its website, Biogen said the discovery was “the result of groundbreaking research and is a testament to Biogen’s steadfast determination to follow the science and do the right thing for patients.”
These abnormal deposits disrupt communication between brain cells which eventually leads to brain cell death.
Aducanumab works by reducing the number of these abnormal deposits present in the brain.
Trial data of over 3,000 people by Biogen shows patients given high doses of aducanumab experienced a “significant” boost to their memory and language skills.
The company said: “Patients who received aducanumab experienced significant benefits on measures of cognition and function such as memory, orientation, and language.
“Patients also experienced benefits on activities of daily living including conducting personal finances, performing household chores such as cleaning, shopping, and doing laundry, and independently traveling out of the home.”
It added that, if approved, “aducanumab would become the first therapy to reduce the clinical decline of Alzheimer’s disease and would also be the first therapy to demonstrate that removing amyloid beta resulted in better clinical outcomes.”
Biogen plans to file a Biologics License Application (BLA) in early 2020 and hopes the treatment will be available in international markets, including Europe and Japan.
Chief executive of Biogen, Michel Vounatsos said the company had already received encouragement from the Food and Drugs Administration.
“With such a devastating disease that affects tens of millions worldwide, today’s announcement is truly heartening in the fight against Alzheimer’s,” he said.
Vounatsos added that the company is hopeful it can offer patients the treatment in the future.