Open Label Extension Study of Nalbuphine HCl ER 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: | September 2014 |
End Date: | January 2016 |
An Open Label Extension Study of the Safety and Anti-Pruritic Efficacy of Nalbuphine HCl ER Tablets in Hemodialysis Patients With Uremic Pruritus
The primary objective of the study is to evaluate the overall safety of nalbuphine HCL ER
tablets during a treatment period of up to 24 weeks.
tablets during a treatment period of up to 24 weeks.
Inclusion Criteria:
- Subject completed participation in the TR02 study
- Subject is currently receiving in-center hemodialysis at the time of consent
Exclusion Criteria:
- Subject receiving or anticipated to be receiving nocturnal dialysis or home
hemodialysis treatment during the study
- Subject received opiates on a daily basis during the 1 week prior to screening
- Other than the TR02 Study Drug, Subject received any investigational drug within 4
weeks prior to Screening
- Subject is a pregnant or lactating female
We found this trial at
34
sites
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