Study of Nalbuphine HCl ER Tablets in Hemodialysis Patients With Uremic Pruritus
Status: | Completed |
---|---|
Conditions: | Allergy |
Therapuetic Areas: | Otolaryngology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 8/30/2018 |
Start Date: | June 2014 |
End Date: | July 2015 |
A Randomized, Double-Blind, Placebo-Controlled, Parallel, 3-Arm Study of the Safety and Anti-Pruritic Efficacy of Nalbuphine HCl ER Tablets in Hemodialysis Patients With Uremic Pruritus
The primary objectives of the study to evaluate the effects of two doses of nalbuphine HCl ER
tablets on the change from baseline in the worst itch Numerical Rating Scale (NRS) in
hemodialysis patients with moderate to severe uremic pruritus and to evaluate the safety and
tolerability in the study population.
tablets on the change from baseline in the worst itch Numerical Rating Scale (NRS) in
hemodialysis patients with moderate to severe uremic pruritus and to evaluate the safety and
tolerability in the study population.
Inclusion Criteria:
- Subject has been receiving in-center hemodialysis for ≥ 3 months and are currently on
a schedule of 3 times a week.
- Subject self-categorized themselves on the Patient Assessed Disease Severity Scale
during Screening
- Subject meets standard of care hemodialysis efficiency guidelines during the three
months prior to completing Screening
- Have demonstrated pruritus intensity on the Itch NRS during screening
- Male or female who are at least 18 years old at the time of Screening
Exclusion Criteria:
- Subject had a significant alteration in dialysis regimen during the Screening Period
- Subject receiving or anticipated to be receiving nocturnal dialysis or home
hemodialysis treatment during the study.
- Subject has pruritus that is believed to be caused by a condition unrelated to
end-stage renal disease
- Has had a history of substance abuse within 6 months prior to completing Screening
- Subject has a known drug allergy to opioids
- Subject is a pregnant or lactating female.
We found this trial at
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