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Source: American Heart Association (AHA)   Released: Tue 16-Apr-2002, 00:00 ET 
Embargo expired: Mon 15-Apr-2002, 16:00 ET 
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New Drug Raises Good Cholesterol

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 Keywords
cholesterol, drug, HDL, cholesterol-lowering drugs, CETP

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After only four weeks, people who took an investigational drug were able to increase their "good" cholesterol levels by 34 percent.

FOR RELEASE:
4 p.m. EDT, Monday
April 15, 2002

CONTACT: For journal copies only,
please call: (214) 706-1396
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American Heart Association rapid access journal brief New drug raises "good" cholesterol

DALLAS, April 16 -- After only four weeks, people who took an investigational drug were able to increase their "good" cholesterol levels by 34 percent, according to a report in today's rapid access Circulation: Journal of the American Heart Association.

Also, 198 people lowered their LDL cholesterol (the "bad" cholesterol) by 7 percent.

The drug, called a CETP inhibitor, works by blocking the action of the cholesteryl ester transfer protein, which is known to lower HDL (the "good" cholesterol).

"CETP represents an important target because this protein plays a key role in HDL metabolism. In fact, a genetic deficiency of CETP is the main reason for high HDL in Asian populations," says study author John Kastelein, M.D., Ph.D., from the Academic Medical Center in Amsterdam, The Netherlands.

The study was designed as a 12-week, multi-center, randomized trial evaluating the efficacy and safety of three different doses of the drug. A clear dose-dependent decrease in CETP activity was observed after one week, reaching a maximum decrease of 37 percent from baseline in the high-dose group after four weeks. After four weeks, participants taking the highest dose, 900 mg, had a 33.9 percent increase in HDL levels.

Except for some mild gastrointestinal side-effects, there were no major adverse effects from the new drug.

"Although these results hold promise, further studies are needed to investigate whether the increase in HDL cholesterol translates into a reduction in coronary artery disease risk," says Kastelein.

Co-authors include Greetje J. de Grooth, M.D.; Jan Albert Kuivenhoven, Ph.D.; Anton F. H. Stalenhoef, M.D., Ph.D.; Jacqueline de Graaf, M.D., Ph.D.; Aeilko H. Zwinderman, Ph.D.; Jan L. Posma, M.D., Ph.D.; and Arie van Tol, Ph.D.

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NR02 -- 1065 (Circ/Kastelein)
Media Advisory: Dr. Kastelein can be reached by phone at +31 20 566 2824; and by e-mail at e.vandongen@amc.uva.nl. (Please do not publish contact information).