A significant portion of the drug’s cost will be covered by Medicare
July 8, 2023
The Alzheimer’s drug Leqembi recently received full approval from the Food and Drug Administration (FDA), marking the first drug to be approved for the disease in two decades. The FDA has cleared the drug for early-stage Alzheimer’s patients, deeming it beneficial based on solid evidence.
The drug has the potential to significantly decrease cognitive decline in Alzheimer’s patients.
Alzheimer’s disease is a severe form of dementia characterised by the decline of thinking, memory, and behaviour skills. It is a progressive disease that gradually worsens, eventually leading to severe disability.
There are currently 6.2 million people living with Alzheimer’s in the United States and 50 million people worldwide. The available treatments for Alzheimer’s disease have been very limited, with the disease often developing slowly without early warning signs.
Improved Accessibility for Alzheimer’s Patients
The availability of the drug in treating Alzheimer’s is a significant breakthrough in the area of dementia care. The drug’s approval comes as welcome news for millions worldwide that have been adversely affected by Alzheimer’s, including Alzheimer’s associations and advocacy groups.
Medicare Coverage to Alleviate Drug Cost Concerns
Leqembi is taken once a month, and the cost of the drug has been a significant concern for patients and families. The drug has been approved for the early stages of Alzheimer’s disease, and Medicare has declared that it will cover a significant portion of the drug’s high cost.
As a result, the drug will be more widely available to those who could benefit from its effects.
Transition From Emergency Use Authorisation to Full Approval
The FDA has previously given Leqembi an emergency use authorization, making it available to patients even before full approval was granted.
However, with the FDA giving its seal of approval to Leqembi, the drug can now be marketed more widely, and physicians can prescribe the drug more freely.
Black-Box Warning for Safety Risks
The availability of the drug comes with significant safety risks, and patients must be carefully monitored. The FDA has also added a black-box warning, which is the highest level of alert that can be added to the label.
The warning highlights the rare but potential occurrence of serious and life-threatening events, such as brain bleeding, which has resulted in fatalities.
The Need for Continued Research & Development
Alzheimer’s has a significant impact on family members, the healthcare system, and society as a whole. It is one of the greatest health concerns of the 21st century, and although significant progress has been made, there is still a long way to go to address the issue fully.
The Way Forward
The FDA’s approval of Leqembi is a hopeful development for those suffering from Alzheimer’s disease and their loved ones. However, it is also important to recognize that the drug is not a cure and is strictly for Alzheimer’s treatment and management.
There is still much to accomplish in the realm of Alzheimer’s disease treatment, and more research must be done in this area to combat the disease’s debilitating effects.
In conclusion, the approval of Alzheimer’s drug Leqembi is a significant milestone in the fight against Alzheimer’s. The drug provides hope to people suffering from Alzheimer’s and their families, but it has a list of safety concerns that users and physicians must critically evaluate and monitor.
The drug’s approval and Medicare coverage will help implement the drug more widely.. It is essential that while we celebrate this milestone, we dedicate ourselves to furthering research and development of therapeutic options for Alzheimer’s disease.
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This article was originally published on IMPAKTER. Read the original article.