Effect of a novel kappa-receptor agonist, nalfurafine hydrochloride, on severe itch in 337 haemodialysis patients: a Phase III, randomized, double-blind, placebo-controlled study

• Published in: Nephrology, dialysis, transplantation dialysis, transplantation, 2010-04, Vol.25 (4), p.1251-1257
• Main Authors: Kumagai, Hiroo, Ebata, Toshiya, Takamori, Kenji, Muramatsu, Taro, Nakamoto, Hidetomo, Suzuki, Hiromichi
• Format: Article
• Language: English
• Subjects: Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy; Biological and medical sciences; Double-Blind Method; Emergency and intensive care: renal failure. Dialysis management; Female; Humans; Intensive care medicine; itch; Male; Medical sciences; Middle Aged; Morphinans - therapeutic use; nalfurafine hydrochloride; Pharmacology. Drug treatments; Placebos; Prospective Studies; Pruritus - drug therapy; Pruritus - etiology; randomized controlled study; Receptors, Opioid, kappa - agonists; Renal Dialysis - adverse effects; Spiro Compounds - therapeutic use; Treatment Outcome; Urinary system; visual analogue scale; κ-receptor agonist
• ISSN: 0931-0509; 1460-2385
• DOI: 10.1093/ndt/gfp588

Background. Pruritus in haemodialysis patients is an intractable disease and substantially impairs their quality of life. Based on the results of our earlier clinical study, we hypothesized that the μ-(mu) opioid system is itch-inducible, whereas the κ (kappa) system is itch-suppressive. Methods. The efficacy and safety of nalfurafine hydrochloride (a novel κ-receptor agonist) were prospectively investigated by randomly (1:1:1) administering 5 or 2.5 μg of the drug or a placebo orally for 14 days using a double-blind design in 337 haemodialysis patients with itch that was resistant to currently available treatments, such as antihistamines. Results. The mean decrease in the visual analogue scale (VAS) from baseline, the study's primary endpoint, was significantly larger in the 5-μg nalfurafine hydrochloride group (n = 114) than in the placebo group (n = 111, P = 0.0002, one-sided test at 2.5% significance level). The decrease in the VAS in the 2.5-μg group (n = 112) was also significantly larger than that in the placebo group (P = 0.0001). The incidence of adverse drug reactions (ADRs) was 35.1% in the 5-μg group, 25.0% in the 2.5-μg group and 16.2% in the placebo group. Moderate to severe ADRs were observed in 10 of the 226 patients. The most common ADR was insomnia (sleep disturbance), seen in 24 of the 226 nalfurafine patients. Conclusions. This Phase III, randomized, double-blind, placebo-controlled, parallel-group, prospective study based on VAS evaluations clearly showed that orally taken nalfurafine hydrochloride effectively reduced itches that were otherwise refractory to currently available treatments in maintenance haemodialysis patients, with few significant ADRs. This novel drug was officially approved for clinical use in January 2009 by the Ministry of Health, Labour and Welfare of Japan.