e have recently completed two studies
confirming the lack of undesirable drug-drug interactions, as well as a
pharmacology study of its effects in the presence and absence of aspirin.
The results of that study provide further evidence that DG041 inhibits
platelet activation and aggregation through a crucial pathway that is not
targeted by existing medications. In order to manage risk and expand our
therapeutic pipeline, we are actively investigating partnership
opportunities for these and earlier stage programs. Our financial results
this year demonstrate our ability to create valuable assets through product
development while leveraging our capabilities to generate near-term revenue
streams," Dr. Stefansson concluded.
Recent highlights include:
Product Development
-- Heart attack. In its drug development program targeting the leukotriene
pathway for the prevention of heart attack, deCODE last month began
enrolling patients for its Phase IIa clinical trial for DG051, the
company's leukotriene A4 hydrolase inhibitor. In Phase I studies
completed earlier this year, DG051 significantly reduced the production
of leukotriene B4 (LTB4) in a dose dependent manner. LTB4 is a pro-
inflammatory molecule that deCODE's gene discovery and functional
biology work identified as a key factor in modulating risk of heart
attack. The Phase I studies showed DG051 to be safe and well-tolerated
at all dose levels tested, with a favourable pharmacokinetic profile.
DG051 was also recently evaluated in a 28-day Phase I study that
further demonstrated that the drug can deliver significant, sustained
reductions in LTB4 levels with once-daily dosing. The Phase IIa is a
randomized, double-blind, placebo-controlled trial that will examine
the impact of DG051 on the production of LTB4 as well as the compound's
pharmacokinetic and safety and tole
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SOURCE deCODE genetics Copyright©2007 PR Newswire. All rights reserved | |
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