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. Author manuscript; available in PMC: 2014 Jul 29.
Published in final edited form as: Curr Pharm Des. 2007;13(15):1607–1616. doi: 10.2174/138161207780765918

Table 3.

Glycosaminoglycans and Mimetics Under Development for the Treatment of Alzheimer’s Disease

HF0402 (C3) Ateroid® AlzhemedTM
Chemistry Very low molecular weight
glycosaminoglycan
Glycosaminoglycan polysulfate 3-amino-1-propanesulfonic acid (tramiprosate)
Administration iv, sc, po po po
Pharmacology Alzheimer’s disease, protection
against neuronal cell death, neuronal
repair, prevention of amyloid peptide-
induced toxicity in the brain via a
number of sites of activity, growth
factor-like neurotrophism
Multi-infarct dementia, ischemic vascular
dementia, old-age dementia, the behav-
ioral effects may be due to normalizing
influence on dopamine neurotransmission
in the nucleus accumbens
Alzheimer’s disease, modify the course of disease
through anti-amyloid activity: binding to soluble
amyloid beta protein, preventing and stopping the
formation and the deposition of amyloid fibrils in the
brain, and reducing the amyloid-induced toxicity on
neuronal and brain inflammatory cells
Adverse effects Little anticoagulant effects, well
tolerated in healthy volunteers
Well tolerated in dementia patients; vital
signs and laboratory measures did not
show clinically significant changes
Well tolerated in patients; most frequent adverse
events were nausea and vomiting
Clinical trial Single dose, Phase I study planned Marketed in Europe and Asia Phase III clinical trials
Website http://www.hunter-fleming.com/ http://www.cornelliconsulting.it http://www.neurochem.com