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Strategies & Market Trends : 2026 TeoTwawKi ... 2032 Darkest Interregnum -- Ignore unavailable to you. Want to Upgrade?


To: TobagoJack who wrote (151907)12/6/2019 8:12:50 AM
From: Logain Ablar  Read Replies (1) | Respond to of 219356
 
TJ:

Along the Alzheimer theme:

10 minute video and the article below it.

fortune.com




To: TobagoJack who wrote (151907)12/6/2019 9:01:33 AM
From: ggersh  Respond to of 219356
 
Let us watch and wait for the brief ;-)



To: TobagoJack who wrote (151907)12/6/2019 10:10:16 AM
From: Julius Wong  Respond to of 219356
 
Alzheimer’s Drug

BIIB and other companies: AVXL, BHVN



To: TobagoJack who wrote (151907)12/7/2019 8:02:24 AM
From: THE ANT1 Recommendation

Recommended By
Horgad

  Read Replies (1) | Respond to of 219356
 
Read Bredesens the end Of Alzheimer's.Eat less than 15 grams of sugar a day, make carbs less than 20% of your diet and put all your eating into a 4-8 hour period. You will not get Alzheimer's or Vascular disease



To: TobagoJack who wrote (151907)12/7/2019 9:43:06 AM
From: Pogeu Mahone1 Recommendation

Recommended By
marcher

  Read Replies (1) | Respond to of 219356
 
That drug is a loser. If the developers cannot determine if it helps it does not!

Please do not give false hope to millions at ridiculous expense where a placebo wouldl work as well.

I believe Biogen has the muscle to get this approved.

If approved the FDA should be shot.

How could Biogen's data hold up?

After at least 5 years of research Biogen says this:

4 December 2019, 23:00 GMT+8
Biogen Inc. stunned Alzheimer’s researchers in March when it said its highly awaited Alzheimer’s treatment aducanumab was unlikely to work.


Than this 6 months later

Biogen Explains How Its Alzheimer’s Drug Went From Poor to Promising

BY ALICE PARK
DECEMBER 6, 2019

It doesn’t happen often—in fact, hardly ever—that a company decides to stop studying a promising drug it’s developing and then a few months later asks the Food and Drug Administration (FDA) to consider approving it.

But that’s exactly what occurred with aducanumab, an Alzheimer’s drug being developed by U.S. pharmaceutical company Biogen and its partner, Eisai, a Japanese pharma outfit. The surprising reversal has left patients, researchers and doctors with a lot of questions—especially since the drug is the first one to, if approved, treat the root causes of Alzheimer’s disease, which affects more than five million people in the U.S. This week, at the Clinical Trials on Alzheimer’s Disease conference in San Diego, Biogen tried to provide some answers in its first detailed public disclosure of the data on its aducanumab study, but the analysis is complex.

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