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Integrase inhibitors: first clear success in human trial.


Merck reported that its experimental integrase inhibitor MK-0518 reduced HIV viral load HIV viral load AIDS A measure of the amount of HIV RNA in blood, expressed as number of copies/mL of plasma. See AIDS, HIV.  98%, in a 10-day monotherapy trial in 28 treatment-naive volunteers. [1] All doses tested, from 100 to 600 mg taken as tablets twice daily, showed a highly statistically significant viral reduction (p=0.001). There were no serious adverse effects in this trial, and no one discontinued the drug due to adverse effects. Based on these results, a 48-week dose-ranging trial of MK-0518 has been started in antiretroviral-naive patients. This information was presented November 18 at the EACS EACS European Association of Chinese Studies
EACS Expeditionary Air Control Squadron (US Air Force)
EACS Senior Chief Engineering Aide (Naval Rating)
EACS Emergency Air Cleaning System
EACS EP/EO Account Control System
 (European AIDS Clinical Society) meeting in Dublin, Ireland.

Background

HIV HIV (Human Immunodeficiency Virus), either of two closely related retroviruses that invade T-helper lymphocytes and are responsible for AIDS. There are two types of HIV: HIV-1 and HIV-2. HIV-1 is responsible for the vast majority of AIDS in the United States.  uses at least three enzymes to reproduce--reverse transcriptase transcriptase /trans·crip·tase/ (-krip´tas) a DNA-directed RNA polymerase; an enzyme that catalyzes the synthesis (polymerization) of RNA from ribonucleoside triphosphates, with DNA serving as a template. , protease, and integrase. These enzymes are obvious targets for designing anti-HIV drugs that block them (but enzymes are certainly not the only targets; there are many more steps in the HIV life cycle that drugs might attack). AZT AZT or zidovudine (zīdō`vydēn'), drug used to treat patients infected with the human immunodeficiency virus (HIV), which causes AIDS; also called  and many other approved drugs block reverse transcriptase. Protease inhibitors came into use around 1996 and revolutionized AIDS treatment (although highly effective HAART HAART highly active antiretroviral therapy.
HAART Highly active antiretroviral therapy, triple combination therapy AIDS The concurrent administration of 2 nucleoside reverse transcriptase inhibitors–eg, AZT and 3TC, and a protease
 combinations without protease inhibitors are also possible). Integrase inhibitors have been the hardest to develop, partly because different protease inhibitors were already used in other areas of medicine, while anti-HIV integrase inhibitors had to be developed from scratch. An earlier integrase inhibitor, S-1360, developed by Shionogi & Co. and GlaxoSmithKline, had to be discontinued because of poor bioavailability bioavailability /bio·avail·a·bil·i·ty/ (bi?o-ah-val?ah-bil´i-te) the degree to which a drug or other substance becomes available to the target tissue after administration.

bi·o·a·vail·a·bil·i·ty
n.
.

The new Merck trial clearly shows that an integrase inhibitor can work in people to lower HIV viral load.

For More Information

Information about this drug will change rapidly, and we do not know which Web or other information will be best. You might check first with the treatment-information sources you already use.

For general news you might try http://news.google.com/--search for "integrase" (quotation marks not necessary). Or for more focus on AIDS-related news, try http://www.aegis.org/search/--"integrase" returns hundreds of articles, mostly very technical, so try "MK-0518" (or any newer drug name that Merck may use in the future).

References

(1.) Morales-Ramirez J.O., Teppler H., Kovacs C., and others, Protocol 004 Team (USA, Canada, Australia). Antiretroviral effect of MK-0518, a novel HIV-1 integrase inhibitor, in ART-naive HIV-1 infected patients. 10th European AIDS Conference / EACS, November 17-20, 2005, Dublin, Ireland [abstract # LBPS LBPS Lender Business Process Services 1/6].
COPYRIGHT 2005 John S. James
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2005, Gale Group. All rights reserved. Gale Group is a Thomson Corporation Company.

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Article Details
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Author:James, John S.
Publication:AIDS Treatment News
Geographic Code:1USA
Date:Oct 1, 2005
Words:376
Previous Article:TMC 125: new results, large phase III trial begins.
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