ILLUMINATE Trial: Difference between revisions

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Revision as of 11:55, 18 September 2013

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Objective

  Normal  0          false  false  false    EN-US  X-NONE  AR-SA                                                                     Raising HDL levels by a combination of torcetrapib, a CETP inhibitor, and atorvastatin, an HGM-CoA reductase inhibitor.

Dates

Start Date

  Normal  0          false  false  false    EN-US  X-NONE  AR-SA                                                                     August 23, 2004

End Date

  Normal  0          false  false  false    EN-US  X-NONE  AR-SA

· Premature Termination on December 2, 2006. Data collection continued till July 15, 2007.

Methods

Results

Study Outcomes

Conclusion

References

@@ Line 3: / Line 3: @@
 {{CMG}}
-==Overview==
-* Clinical research on [[torcetrapib]] stopped because of increased incidence of cardiovascular events as an adverse effect of the drug.<ref name="pmid17984165">{{cite journal |author=Barter PJ, Caulfield M, Eriksson M, ''et al.'' |title=Effects of torcetrapib in patients at high risk for coronary events |journal=[[The New England Journal of Medicine]] |volume=357 |issue=21 |pages=2109–22 |year=2007 |month=November |pmid=17984165 |doi=10.1056/NEJMoa0706628 |url=}}</ref>
+==Objective==
-* [[Torcetrapib]] side-effects include a significant increase in systolic blood pressure ([[hypertension]]) and a significant reduction in [[serum potassium]] ([[hypokalemia]]) levels.
+   Normal  0          false  false  false    EN-US  X-NONE  AR-SA                                                                     Raising HDL levels by a combination of torcetrapib, a CETP inhibitor, and atorvastatin, an HGM-CoA reductase inhibitor.
+==Dates==
+===Start Date===
+   Normal  0          false  false  false    EN-US  X-NONE  AR-SA                                                                     August 23, 2004
+===End Date===
+   Normal  0          false  false  false    EN-US  X-NONE  AR-SA
+·         Premature Termination on December 2, 2006.  Data collection continued till July 15, 2007.
+==Methods==
+==Results==
+==Study Outcomes==
+==Conclusion==
 ==References==

v t e Lipopedia
Basic Science	Cholesterol • Triglyceride Lipoprotein metabolism and transport Lipoprotein: Chylomicron • Chylomicron remnant • HDL • IDL • LDL • Lipoprotein(a) • VLDL • Lipoprotein-X Apolipoprotein: APOA (1, 2, 4, 5) • APOB ( Apolipoprotein B-48, Apolipoprotein B-100) • APOC (1, 2, 3, 4) • APOD • APOE • APOH • APOJ • APOL • APOM • Apo(a) Lipoprotein receptor: LDL receptor • Soluble low density lipoprotein receptor-related protein (sLRP) • Apolipoprotein E Receptor 2 • Scavenger receptor • Scavenger receptor A • Scavenger receptor B • VLDL receptor Lipoprotein enzymes: Lipoprotein lipase • Lipoprotein-associated phospholipase A2 (Lp-PLA2) • Cholesterylester transfer protein ( Acetyl-CoA C-acyltransferase, Lecithin-cholesterol acyltransferase) • Microsomal triglyceride transfer protein • ABCA1 Genes: Low density lipoprotein receptor gene family • Microsomal triglyceride transfer protein • ABCA1
Lipoprotein Disorders	Lipoprotein disorders Primary lipoprotein disorders: Familial hyperchylomicronemia (Type I) • Familial hypercholesterolemia (Type IIA) • Familial combined hyperlipidemia (Type IIB) • Dysbetalipoproteinemia (Type III) • Primary hypertriglyceridemia (Type IV) • Mixed hyperlipoproteinemia (Type V) Secondary lipoprotein disorders
Abnormal Laboratory Lipid Profile	Low chylomicron • Low chylomicron remnant • Low HDL • Low IDL • Low LDL • Low lipoprotein(a) • Low VLDL High chylomicron • High chylomicron remnant • High HDL • High IDL • High LDL • High Lipoprotein(a) • High VLDL

ILLUMINATE Trial: Difference between revisions

Revision as of 11:55, 18 September 2013

Objective

Dates

Start Date

End Date

Methods

Results

Study Outcomes

Conclusion

References

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