SI
SI
discoversearch

We've detected that you're using an ad content blocking browser plug-in or feature. Ads provide a critical source of revenue to the continued operation of Silicon Investor.  We ask that you disable ad blocking while on Silicon Investor in the best interests of our community.  If you are not using an ad blocker but are still receiving this message, make sure your browser's tracking protection is set to the 'standard' level.
Biotech / Medical : Vasogen -- Ignore unavailable to you. Want to Upgrade?


To: Tom Drolet who wrote (26)11/10/2003 9:58:34 AM
From: caly  Respond to of 58
 
Very nice sounding! Would be interested in hearing anything you find out.

"Preclinical findings demonstrating the ability of VP025 to significantly reduce key measures of inflammation and cell death in the brain and to improve physiological measurements that correlate with memory and learning activity were presented this past weekend at the 33rd Annual Meeting of the Society for Neuroscience in New Orleans, by Professor Marina Lynch, PhD, and her team from the Department of Physiology, Trinity College, Dublin, Ireland. The inflammation-induced loss of memory function, measured by the ability to sustain long-term potentiation, was significantly (p less than 0.001) reduced by VP025. This improvement was associated with significant (p less than 0.05) reductions in inflammatory markers in the hippocampus, the site of memory and learning in the brain, including the stress activated kinase c-Jun N-terminal kinase (JNK) and the pro-inflammatory cytokine interleukin 1- (IL-1 ). Furthermore, VP025 administration resulted in an increase in the hippocampal levels of the anti-inflammatory cytokine interleukin-4 (IL-4) (p less than 0.05) in this model."



To: Tom Drolet who wrote (26)11/10/2003 12:55:24 PM
From: russet  Read Replies (1) | Respond to of 58
 
Quite a bit of discussion over here about Vasogen, including the new anti inflammatory liposome. You must ask the moderator for access to the talksite, and he/she wants you to post something about biotech once a month. Very good discussions on several companies and drugs.

stockhouse.ca

Here is a snippet,...

People often confuse orphan drug status with fast track status. Orphan drug status is for drugs addressing small markets, i.e. less common illnesses. There is zero chance that Alzheimer's would ever be considered such an illness. If VAS wants to get orphan drug status for their new synthetic IMT (SAB's), they would need to go after Lou Gehrig's disease (ALS). The other potential applications, such as Alzheimer's, Parkinson's, stroke, and MS, are all major illnesses. The possibility of fast track status, on the other hand is realistic for the SAB's. Fast track means the FDA will review the application to market the product more quickly, with the final review taking only about 6 months instead of 12+ months. I believe there are other short cuts along the way as well. Of course, this point is contingent on the SAB's being considered a drug therapy, as opposed to a device, which seems like the likely scenario. Although regular IMT qualifies as a device, the SAB's would seem to be a drug, and as such, would require the usual 3 Phases of clinical trials.
fid, the abstract about the SAB's is indeed very technical, but if you want a plainer description of the portion of the abstract which describes the product, they are liposomes, which is a fatty substance, shaped into a generally spherical shape, and filled with a substance, which I believe is called phosphatadylserine, which works through to the surface of the liposome. When certain immune cells engulf/ingest these phosphatadylserine-presenting liposomes, they react in the same manner as when they ingest the apoptotic cells produced by the regular IMT. In other words, they respond by increasing their release of anti-inflammatory cytokines and lowering their release of inflammatory cytokines. In effect, the SAB's mimic the apoptotic cells produced by regular IMT. Apparently, these liposomes are able to cross the blood-brain barrier, which is why this technique will be used for the neurological indications. Regular IMT will continue to be used for the cardiovascular indications. I have seen some slides of the brain inflammation results in rats, and they are quite impressive. Of course, it is an awfully long way from rats to humans. It will be interesting to see which indication VAS chooses for the SAB's, and whether they will work as well as regular IMT.

The above description may not be 100% exact, but it's pretty close.