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Dutasteride
Dutasteride More Dutasteride Information | More | Press | Trials | Press | FDA Glaxo Trials EFFECTIVE SUPPRESSION OF DIHYDROTESTOSTERONE (DHT) BY DUTASTERIDE, A NOVEL, DUAL 5 ALPHA REDUCTASE INHIBITOR. Introduction and Objectives DHT is formed from testosterone (T) by Type 1 and Type 2 5 a reductase enzyme (5AR). DHT plays a key role Dutasteride is the first dual inhibitor of both 5AR isozymes. We compared hormonal effects of dutasteride with placebo and finasteride, a Type 2 5AR inhibitor. A second group of 313 subjects was studied for 24 weeks and received dutasteride at 0.01, 0.05, 0.5, 2.5, or 5.0mg, placebo, or 5mg finasteride daily. Studies were randomized, double blinded, with a parallel group design. All subjects had BPH, prostate volume >= 30ml or IPSS >= 8. Dutasteride groups were compared to placebo and finasteride by a general linear model with Dutasteride suppressed DHT in dose related fashion with maximal suppression >= 95% at the 5.0mg dose. The lowest maximally effective dose was 0.5mg, with 90% DHT suppression at 4 wks, increasing to 94% at 24 wks, while finasteride suppressed DHT by 67% and 76% respectively. T rose in conjunction with DHT suppression, ranging from 9 to 27%, but mean T levels with both dutasteride and finasteride remained within the normal range. Dutasteride, a dual inhibitor of 5AR, achieved significantly greater suppression of DHT with less subject variability compared to finasteride. The increase in T at maximally effective doses of dutasteride was not considered clinically significant as mean T levels remained in the normal range. Dutasteride was well tolerated at all dose levels studied with a safety profile comparable to placebo except for a mild decrease in libido also noted with finasteride. The consistent and increased suppression of DHT by dutasteride may show greater clinical benefit in the treatment of BPH. This is currently being investigated with the 0.5mg dose in large-scale phase III clinical trials. GlaxoWellcome Research and Development. More Dutasteride Information | More | Press | Trials | Press | FDA
Dutasteride
Richard V Clark, David J Hermann, Hoda Gabriel, Timothy H Wilson, Betsy B Morrill, and Stuart Hobbs.
Research Triangle Park, NC (presented by Dr. Clark)
in the development and progression of benign prostatic hyperplasia (BPH).
Methods
One group of 53 subjects was studied for 4 weeks and received dutasteride at 0.1, 0.5, 2.5, 5.0mg and 2.5mg
with a 40mg loading dose, placebo, or 5mg finasteride daily.
pairwise comparisons, and a sigmoid Emax model for DHT dose response.
Results
Laboratory studies and ECG's remained normal during the studies. Adverse events were typical, non-specific
events and were reported at comparable rates to placebo for both compounds, except for decreased libido with 5.0mg dutasteride and finasteride.
Conclusions
Source of funding