This multiple-dose study of DMP 504, a hydrogel bile acid sequestrant, employed a randomized, double-blind, sequential-cohort design with placebo (blinded) and open-label cholestyramine (CS) controls. Ninety-three healthy primary hypercholesterolemic subjects (serum LDL cholesterol 130 to 200 mg/dL;
DMP 504, a novel hydrogel bile acid sequestrant: II. Lipid-lowering pharmacology in the hamster
โ Scribed by Peter J. Gillies; Jeffrey T. Billheimer; Verdell A. Blackston; Debra A. Cromley; Garret D. Figuly; Robert T. Fischer; Sandra J. Germain; Helen E. Godonis; Mary A. Gorko; Lisa C. Grimminger; Susan J. Harvey; James H. Jensen; Cathy J. Kieras; Susan D. Royce; Henry C. Pautler; Edward J. Shimshick; Rosanne C. Stevenson; James W. Hainer
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 189 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0272-4391
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โฆ Synopsis
DMP 504 is a novel hydrogel bile acid sequestrant in development for the treatment of moderate hypercholesterolemia. The drug is a condensation polymer synthesized from 1,10-dibromodecane and 1,6-diaminohexane. In vitro binding studies demonstrate that DMP 504 is superior to cholestyramine (CS) with respect to equilibrium binding capacity and affinity for bile acids. The goals of the research reported herein were to assess the in vivo hypolipidemic activity of DMP 504, to elucidate the mechanism of action of DMP 504, and to determine the potency of DMP 504 relative to CS in hamsters. Six dose groups each of DMP 504 and CS were included in the study, along with an untreated control group. The DMP 504 doses ranged from 20-1,000 mg/kg/day for 14 days; CS doses ranged from 50-2,000 mg/kg/day for 14 days. There were 48 animals per dose group; drugs were administered in the feed. At the midpoints of the dose-response curves, DMP 504 was superior to CS with respect to increasing the output of fecal bile acids (7-fold) and sterols (3-fold), increasing the activity of hepatic cholesterol 7ฮฑ-hydroxylase activity (C7ฮฑOH) (6-fold), and decreasing the circulating levels of total serum cholesterol (6-fold), non-HDL cholesterol (6fold), and HDL cholesterol (4-fold). Neither DMP 504 nor CS had significant effects on serum triglycerides or apo-B. In summary, DMP 504 is a new bile acid sequestrant that is mechanistically similar to CS, but is, on average, 6-fold more potent.
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