2010
DOI: 10.1016/j.urology.2009.09.077
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Dose-ranging Study of the Luteinizing Hormone-releasing Hormone Receptor Antagonist Cetrorelix Pamoate in the Treatment of Patients With Symptomatic Benign Prostatic Hyperplasia

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Cited by 20 publications
(7 citation statements)
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“…(42) A phase II, randomized, placebocontrolled study in men with BPH/LUTS conducted in Eastern Europe demonstrated promising results. (43) Following this, phase III studies were conducted in the United States and Europe. In the US study, cetrorelix showed no statistically significant benefit in improving IPSS.…”
Section: Gonadotropin-releasing Hormone (Gnrh) Antagonistsmentioning
confidence: 99%
“…(42) A phase II, randomized, placebocontrolled study in men with BPH/LUTS conducted in Eastern Europe demonstrated promising results. (43) Following this, phase III studies were conducted in the United States and Europe. In the US study, cetrorelix showed no statistically significant benefit in improving IPSS.…”
Section: Gonadotropin-releasing Hormone (Gnrh) Antagonistsmentioning
confidence: 99%
“…53 In a Phase II study, intramuscular injection of cetrorelix 60 mg led to a 6-month sustained 4-point reduction in IPSS versus placebo administration, an effect, however, that was not observed in Phase III RCTs that followed. 54 , 55 …”
Section: Treatment Modalities Currently Under Investigationmentioning
confidence: 99%
“…The LHRH antagonist, cetrorelix, has beneficial effects on LUTS in BPH patients [53][54][55][56][57]. A study with cetrorelix showed short-term administration produced long-term LUTS improvement and decreased prostate volume [53].…”
Section: Luteinizing Hormone-releasing Hormone Antagonistsmentioning
confidence: 99%
“…In a phase II multidose study [55], cetrorelix was well tolerated, effective with rapid onset and persistent response. Debruyne et al [56] compared the efficacy of four doses of cetrorelix in a sustained release formulation allowing more convenient administration. After a single-blind, placebo, run-in phase of 4 weeks, treatment was administered at 2-week intervals as follows: 30 þ 30 mg, 30 þ 30 þ 30 mg, 60 þ 30, 60 þ 60 mg cetrorelix, or placebo.…”
Section: Luteinizing Hormone-releasing Hormone Antagonistsmentioning
confidence: 99%