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ACT-AD Urges Congress to Provide FDA with $2.8B in FY 2018

Letter states that the FDA's role in the development of new treatments is vital

The ACT-AD Coalition has sent a letter to the chairmen and ranking members of the U.S. Senate’s and House of Representatives’ Appropriations Subcommittees on Agriculture, Rural Development, Food and Drug Administration, and Related Agencies requesting they provide the U.S. Food and Drug Administration (FDA) with $2.8 billion in budget authority appropriations in Fiscal Year 2018. This would represent a $78 million increase over FY 2016 appropriated levels.

The letter notes this increase “would allow the agency to maintain their active engagement with the Alzheimer’s disease community and put us closer to more effective treatments and a cure for this disease.”

The letter points out that while Alzheimer’s disease affects five million Americans, is the sixth leading cause of death in the United States, and currently costs the health care system more than $200 billion a year, there are no new medicines available to prevent, delay, or halt the progression of Alzheimer’s disease.

Given the present and future impact this disease will have on the U.S., the FDA’s role in the development of new treatments is vital. A summary of some of its Alzheimer’s-focused activities include:

  • A report on targeted drug development in 2015 that identified gaps in knowledge believed to be hindering progress in the discovery and testing stages of new drugs for Alzheimer’s disease.
  • Participation in two annual meetings convened by ACT-AD and other scientific meetings to shed light on how industry, the National Institutes of Health (NIH), and other organizations can align to more quickly fill these critical research gaps
  • A draft guidance to guide clinical trials focused on treatment of the disease before the onset of noticeable symptoms
  • Involvement in collaborative efforts to find biomarkers that can identify Alzheimer’s patients before they show symptoms, distinguish the rate of disease progression among Alzheimer’s patients, and predict the clinical outcomes of treatments

The letter concludes, “We are fortunate that there are more than 70 compounds in various stages of clinical development for Alzheimer’s disease. The FDA must continue to be actively involved at each stage of drug development to enable these compounds to potentially change the course of Alzheimer’s disease and allow the U.S. to avert a looming fiscal and public health crisis. The actions taken by the FDA in the Alzheimer’s disease space are resource intensive and can only be sustained with adequate funding from Congress each year. Strong support for the FDA in FY 2018 will show that you acknowledge the important role the agency plays in ensuring that we are better prepared to meet the challenges posed by Alzheimer’s disease.”

Read the full letter here.

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  FDA Letter (300K PDF)
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