Nalbuphine ER Effects of Liver Disease on Pharmacokinetics and Itch

PHASE1UnknownINTERVENTIONAL
Enrollment

56

Participants

Timeline

Start Date

October 24, 2018

Primary Completion Date

November 30, 2020

Study Completion Date

December 31, 2020

Conditions
NalbuphineHepatic Impairment
Interventions
DRUG

Nalbuphine ER

Cohort 1: 6-8 subjects will receive 1 dose of 27mg and observed for 4 days. Cohort 2: 6-7 subjects will receive 1 dose of 54 mg and observed for 4 days. Cohort 3: 6-7 subjects will receive 1 dose of 108 mg and observed for 4 days. Cohort 4: 6-8 subjects will receive 1 dose of 162 mg and observed for 4 days. Cohort 5: 6-8 healthy subjects will receive dosing of NAL ER and observed for 4 days.

DRUG

Nalbuphine ER -

Cohort 6: • 6-8 subjects with mild hepatic impairment and 6-8 subjects with moderate hepatic impairment. Doses will be subsequently escalated for each subject starting at 27 mg on Day 1 to twice daily, 12 hours apart, 27 mg, 54 mg, 108 mg, and 162 mg over 13 days.

Trial Locations (3)

32809

03, Orlando

33136

01, Miami

33146

02, Miami

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

Syneos Health

OTHER

lead

Trevi Therapeutics

INDUSTRY