Loading clinical trials...
Loading clinical trials...
An Open Label Extension Study of the Safety and Anti-Pruritic Efficacy of Nalbuphine HCl ER Tablets in Prurigo Nodularis Patients
The primary objective of the study is to evaluate the overall safety of nalbuphine HCL ER tablets during a treatment period of up to 50 weeks.
Age
18 - 75 years
Sex
ALL
Healthy Volunteers
No
University of Münster
Münster, Germany
Start Date
August 15, 2015
Primary Completion Date
September 3, 2017
Completion Date
September 3, 2017
Last Updated
May 21, 2025
36
ACTUAL participants
nalbuphine HCl ER
DRUG
Lead Sponsor
Trevi Therapeutics
NCT06342713
NCT06516952
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06779136