All GLG News Analyses Filed Under: Cardiology
Posted January 14, 2008
Schering releases ENHANCE data today
Analysis of: Schering releases ENHANCE data today | www.tradingmarkets.com
Author: GLG Member Program Contributor
Analysis of: Schering releases ENHANCE data today | www.tradingmarkets.com
Author: GLG Member Program Contributor
Physicians have several possible conclusions that can be taken; These include:
- the trial is flawed - the selection of patients with much less CIMT than previous trials such as ASAP and ARBITER flaws the study
- the failure to meet the trial endpoint is only a surrogate and clinical trial data...
Posted January 14, 2008
Genzyme and Isis Announce Strategic Alliance Including Exclusive Worldwide License of Mipomersen
Analysis of: Genzyme and Isis Announce Strategic Alliance Including Exclusive Worldwide License of Mipomersen | www.pipelinereview.com
Author: GLG Member Program Contributor
Analysis of: Genzyme and Isis Announce Strategic Alliance Including Exclusive Worldwide License of Mipomersen | www.pipelinereview.com
Author: GLG Member Program Contributor
At present despite the statins we have, many do not reach goal. In fact. it may be that that goal is not adequate as we have still a major issue with cardiovascular disease. This product may prove to be a further advance along this line.
Posted January 9, 2008
Daiichi Sankyo, Lilly Submit New Drug Application for Investigational Antiplatelet Drug, Prasugrel, with U.S. Food and Drug Administration
Analysis of: Daiichi Sankyo, Lilly Submit New Drug Application for Investigational Antiplatelet Drug, Prasugrel, with U.S. Food and Drug Administration | www.rxtimes.com
Author: GLG Member Program Contributor
Analysis of: Daiichi Sankyo, Lilly Submit New Drug Application for Investigational Antiplatelet Drug, Prasugrel, with U.S. Food and Drug Administration | www.rxtimes.com
Author: GLG Member Program Contributor
This may be a better drug than plavix, but it also has more serious bleeding problems. It will likely be approved, but with restictions if it is.
Posted December 21, 2007
Ablynx Reports Positive Phase I Results for Its Anti-Thrombotic Nanobody(R), ALX-0081
Analysis of: Ablynx Reports Positive Phase I Results for Its Anti-Thrombotic Nanobody(R), ALX-0081 | www.pipelinereview.com
Author: GLG Member Program Contributor
Analysis of: Ablynx Reports Positive Phase I Results for Its Anti-Thrombotic Nanobody(R), ALX-0081 | www.pipelinereview.com
Author: GLG Member Program Contributor
vWF is one of a number of attractive antiplatelet targets which include P2Y112, GIIb/IIIa, to name a few. Currently Medicines Company's Cangrelor, a small molecule against P2Y12 is quite far along in development. In addition, Archemix just published results of its Phase I trial with its anti-vWF...
Posted December 20, 2007
Ablynx Reports Positive Phase I Results for Its Anti-Thrombotic Nanobody(R), ALX-0081
Analysis of: Ablynx Reports Positive Phase I Results for Its Anti-Thrombotic Nanobody(R), ALX-0081 | www.pipelinereview.com
Author: GLG Member Program Contributor
Analysis of: Ablynx Reports Positive Phase I Results for Its Anti-Thrombotic Nanobody(R), ALX-0081 | www.pipelinereview.com
Author: GLG Member Program Contributor
Drug will target early key adhesion events that facilitate platelet adherence to exposed subendothelium after injury- may have significant influence in blocking subsequent events leading to thrombosis; however, it will be interesting to see if this drug class will increase bleeding or reduce wound...
Posted December 20, 2007Ablynx may have a benign antibody for 2 "malignant" conditions
Analysis of: Ablynx Reports Positive Phase I Results for Its Anti-Thrombotic Nanobody(R), ALX-0081 | www.pipelinereview.com
Author: Kenneth Algazy, Clinical Professor of Medicine University of Pennsylvania School of Medicine - CC
A novel antibody, ALX-0081, that is well tolerated nd is directed against von Willebrand Factor (anti-vWF), that is strongly implicated in taking part in acute coronary events and conclusively responsible for the disastrous outcomes of thrombotic thrombocytopenic purpura (TTP).
Posted December 20, 2007
Amarin Commences First Clinical Trial in Cardiovascular Program
Analysis of: Amarin Commences First Clinical Trial in Cardiovascular Program | www.pipelinereview.com
Author: GLG Member Program Contributor
Analysis of: Amarin Commences First Clinical Trial in Cardiovascular Program | www.pipelinereview.com
Author: GLG Member Program Contributor
Niacin is the most potent approved HDL-raising agent with evidence for cardiovascular benefit. Flush is the limiting side-effect. EPA (a major component of omega 3 fish oil) decreases triglycerides and may have antiarrhythmic properties.
Posted December 17, 2007
NATRECOR Authorized In Canada For Treatment Of Acute Decompensated Heart Failure
Analysis of: NATRECOR Authorized In Canada For Treatment Of Acute Decompensated Heart Failure | www.medicalnewstoday.com
Author: GLG Member Program Contributor
Analysis of: NATRECOR Authorized In Canada For Treatment Of Acute Decompensated Heart Failure | www.medicalnewstoday.com
Author: GLG Member Program Contributor
This is great news for Canada. This is the first new drug approved for the treatment of acute heart failure since 1989, when milrinone was approved. Nesiritide was approved in the United States in 2001. Since then, it has proven to be of great benefit in patients with acute heart failure,...
Posted December 17, 2007
NATRECOR Authorized In Canada For Treatment Of Acute Decompensated Heart Failure
Analysis of: NATRECOR Authorized In Canada For Treatment Of Acute Decompensated Heart Failure | www.medicalnewstoday.com
Author: GLG Member Program Contributor
Analysis of: NATRECOR Authorized In Canada For Treatment Of Acute Decompensated Heart Failure | www.medicalnewstoday.com
Author: GLG Member Program Contributor
so far we have been restricted to the use of vasopressor in the perioperative setting with its adverse consequences on microvasculature particularly renal.with the availability of natrecor this category of patients where peripheral vasoconstriction is undesirable ,will immensely benefit. weaning off...
Posted December 11, 2007The Importance of the FDA's Stance on Merck's (and now GSK's) OTC Mevacor
Analysis of: FDA weighs over-counter cholesterol drug | news.yahoo.com
Author: Jeff Stier, Associate Director American Council on Science and Health
How will the FDA rule? What are the potential public health benefits? Are there risks of OTC statins? Watching closely, will be Glaxo Smithkline (GSK), which will market OTC Mevacor. Approval could impact sales of Pfizer's Lipitor and other statins made by pharma's including AstraZeneca, Novartis...
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