At Risk for Huntington's Disease

HD is a genetically caused brain disorder that causes uncontrollable bodily movements and robs people's ability to walk, talk, eat, and think. The final result is a slow, ugly death. Children of parents with HD have a 50-50 chance of inheriting the disease. There is no cure or treatment.

Showing posts with label biomarkers. Show all posts
Showing posts with label biomarkers. Show all posts
Monday, March 02, 2020

CHDI head scientist Pacifici: ‘hang on in the learning roller coaster ride of Huntington’s disease clinical trials’

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With historic clinical trials now aiming for the first effective treatments for Huntington’s disease, affected individuals and their fami...
Thursday, December 20, 2018

Roche announces U.S., Canada sites for Phase 3 clinical trial of Huntington’s disease drug

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Pharmaceutical firm Roche has announced 26 planned sites in the U.S. and Canada for its historic Phase 3 clinical trial of a gene-silenc...
Friday, November 09, 2018

Roche announces first sites for key Huntington’s disease observational study

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Pharmaceutical firm Roche has identified nine sites in the U.S. and Canada for an observational study that will seek to answer key quest...
Tuesday, June 27, 2017

Ionis Huntington’s disease drug a step closer to a critical Phase 2 study

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Ionis Pharmaceuticals has made two positive announcements about the historic Phase 1 clinical trial of its gene-silencing drug for Hunti...
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Thursday, February 25, 2016

Chief Huntington’s disease drug hunter: ‘every confidence first treatments’ in the works

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Surveying the vast progress in Huntington’s disease research and a “blitz” of clinical trials now in progress, a key scientific leader in ...
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