Sign Up for the Alzheimer’s Prevention Registry

alzheimers prevention registry


Launching a research study often takes years of work, and most of the effort occurs behind the scenes. The exciting news is that several of these studies have just launched or are close to being ready to start recruiting participants through the Alzheimer’s Prevention Registry. And more studies will launch in the coming years. Here is a snapshot of a few of the studies that will be taking place in the United States and other countries around the world:

  • A trial in 1000 adults ages 65-85 who have evidence of amyloid plaque build up in their brain based on a screening PET scan, and  who are at risk for Alzheimer’s disease but are still cognitively healthy to determine whether an experimental medication may delay cognitive decline
  • A trial in nearly 6,000 adults ages 65-83 to learn about the genetic risk for developing mild cognitive impairment due to Alzheimer’s disease and whether an experimental medication might delay the symptoms
  • Two trials in a rare, hereditary form of early-onset Alzheimer’s with experimental medications to determine if treatment delays cognitive impairment
  • And many more.

Imagine having tens of thousands of volunteers awaiting an e-mail from the Registry announcing that a study is ready to begin enrollment in their communities.  Researchers could quickly screen and fill their enrollment sites in a matter of weeks or months, not years. Saving this precious time means we get to answers faster.
This is why the Alzheimer’s Prevention Registry will play a vital role in these and other prevention trials.

Take action:   While researchers work to get these and other studies ready, you can help by continuing to encourage your friends and family to sign up for the Registry.

 

 

The Economist recognises Genentech for corporate innovation

Genentech was named the winner of the Corporate Award for its consistent and impressive record in breakthrough research and innovation at The Economist’s Innovation Awards on  Monday November 25th, 2013.

Genentech Web

The Corporate award celebrates Genentech’s track record in research and innovation. Genentech was founded by biochemist Herbert Boyer and venture capitalist Robert Swanson in 1976. It has been a wholly owned subsidiary of the Roche Group since 2009. Widely considered the founder of the biotech industry, the company changed the face of medicine when it became the first to scale up protein-manufacturing from the small quantities used for research to the much larger quantities needed to treat patients. The firm’s achievements include the development of the first recombinant DNA medicine ever marketed, the first targeted medicine approved to treat cancer and the first medicine shown to improve vision in the most common cause of blindness in adults.
Genentech’s research scientists have earned more than 10,500 patents and brought breakthrough medicines to people with serious diseases such as cystic fibrosis, cancer, rheumatoid arthritis and stroke. Overall, it has 35 medicines on the market and at least 30 more in clinical development. In 2012, sales of Genentech’s medicines in the United States were CHF13.856 billion.

Eye Test Identifies Alzheimer’s

(BUSINESS WIRE)–Nov 15, 2013–Cognoptix disclosed today at the ‘Clinical Trials on Alzheimer’s Disease’ (CTAD) scientific meeting the strong results of a multi-site clinical trial of its SAPPHIRE II eye test, which is designed to identify Alzheimer’s Disease (AD) patients via a beta-amyloid (Ab) signature in their eyes.Continue reading

FTC Seeking Public Comment on Follow-On Biologics

The Federal Trade Commission (FTC) is seeking public comment on follow-on biologics.

In addition, the FTC will hold a public workshop on December 1oth.

The Follow-On Biologics Workshop: Impact of Recent Legislative and Regulatory Naming Proposals on Competition

The  Federal Trade Commission announces it will hold a workshop to explore  competition issues involving biologic medicines and follow-on biologics. As  described in the Federal Register Notice, the workshop will focus on a few key  issues, inter alia:

  • The potential impact of state regulations affecting competition.
  • How regulations, if necessary, might be structured to facilitate competition  while still protecting patient health and safety.
  •   How naming may affect competition.
  • The experience of other countries with follow-on biologic competition.

The  Federal Register Notice poses a series of questions about which the FTC seeks  public comment. The FTC will take these comments into account in its  examination of these topics.

Previous Biologics Workshops and Report:

Event Details

WHEN:

December 10, 2013 Time: 9am – 5pm

WHERE:

FTC Conference Center

601 New Jersey Avenue, NW

Washington, DC

Learn more at http://www.ftc.gov/opp/workshops/biologics/#nj