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Cited 63 time in webofscience Cited 75 time in scopus
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Efficacy and Safety of Mirodenafil, A New Oral Phosphodiesterase Type 5 Inhibitor, for Treatment of Erectile Dysfunction

Authors
Paick, Jae-SeungAhn, Tai Y.Choi, Hyung K.Chung, Woo-SikKim, Je J.Kim, Sae C.Kim, Sae W.Lee, Sung W.Min, Kweon S.Moon, Ki H.Park, Jong K.Park, KwangsungPark, Nam C.Suh, Jun-KyuYang, Dae Y.Jung, Hyung-Gi
Issue Date
Nov-2008
Publisher
WILEY
Keywords
Erectile Dysfunction; PDE5; Mirodenafil
Citation
JOURNAL OF SEXUAL MEDICINE, v.5, no.11, pp 2672 - 2680
Pages
9
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF SEXUAL MEDICINE
Volume
5
Number
11
Start Page
2672
End Page
2680
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/35673
DOI
10.1111/j.1743-6109.2008.00945.x
ISSN
1743-6095
1743-6109
Abstract
Mirodenafil is a newly developed oral phosphodiesterase type 5 inhibitor, currently under investigation as a treatment for erectile dysfunction (ED). We investigated the efficacy and safety of on demand mirodenafil therapy at fixed doses (50 and 100 mg) in Korean men with a broad range of ED. A multicenter, randomized, double-blind, placebo-controlled, parallel-group, fixed-dose study was conducted with 223 subjects who were randomized to placebo or mirodenafil at fixed doses of 50 or 100 mg for 12 weeks on an "as needed" basis. Primary efficacy measures were scores on the International Index of Erectile Function (IIEF) Question 3 (Q3) and Question 4 (Q4). Secondary efficacy measures included all domain scores of the IIEF, Sexual Encounter Profile Question 2 (SEP2), Sexual Encounter Profile Question 3 (SEP3), the Global Assessment Question (GAQ), and the Life Satisfaction Checklist (LSC). Safety assessments included laboratory tests, vital signs, physical examination, 12-lead electrocardiogram recordings, and patients' reporting of adverse events. Mirodenafil 50 and 100 mg groups showed a significantly greater increase in IIEF Q3 (P = 0.0001, P < 0.0001, respectively) and Q4 scores (both P < 0.0001) at the end point compared with the placebo group. And mirodenafil in both doses significantly improved the scores of all five domains of the IIEF, SEP2, and SEP3 as well as the percentages of patients responding positively to the GAQ compared with the placebo group. As for LSC scores, the two mirodenafil groups showed significantly greater improvements in items regarding life as a whole, sexual life, and partner relationship than the placebo group. Most treatment-associated adverse events were of mild intensity, resolving spontaneously. Mirodenafil, in doses of 50 or 100 mg, significantly improved erectile function and were well tolerated in a representative population of Korean men with broad-spectrum ED of various etiologies and severities. Paick J-S, Ahn TY, Choi HK, Chung W-S, Kim JJ, Kim SC, Kim SW, Lee SW, Min KS, Moon KH, Park JK, Park K, Park NC, Suh J-K, Yang DY, and Jung H-G. Efficacy and safety of mirodenafil, a new oral phosphodiesterase type 5 inhibitor, for treatment of erectile dysfunction. J Sex Med 2008;5:2672-2680.
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