A Study of Nalbuphine (Extended Release) ER in Idiopathic Pulmonary Fibrosis (IPF) for Treatment of Cough

Idiopathic Pulmonary Fibrosis Clinical Trial

— CANAL  

Official title:

Phase 2, Double-blind, Randomized, Placebo-controlled, Two-Treatment, Two-Period Crossover Efficacy and Safety Study in Idiopathic Pulmonary Fibrosis (IPF) With Nalbuphine ER Tablets for the Treatment of Cough

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04030026
• Other study ID #: TR12
• Secondary ID: 2018-004744-31
• Status: Completed
• Phase: Phase 2
• Start date: August 8, 2019
• Est. completion date: May 27, 2022

Study information

• Verified date: May 2023
• Source: Trevi Therapeutics
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To investigate the efficacy and safety of Nalbuphine ER (NAL ER) tablets in subjects diagnosed with Idiopathic Pulmonary Fibrosis (IPF) and evaluate it's treatment of cough in these patients. This is a two-treatment, 2-period crossover study. Subjects will be randomized in Treatment Period 1 to either NAL ER or matching placebo and evaluated for approximately 21 days. After completion of the first phase, subjects who received NAL ER will crossover to placebo and subjects who received placebo will crossover to NAL ER to complete Treatment Period 2.

Description:

This is a double-blind, randomized, placebo-controlled, 2-treatment, 2-period crossover efficacy and safety study in IPF subjects with NAL ER tablets for the treatment of cough. The study consists of 2 treatment periods of 3 weeks, each followed by a washout period of 2 weeks. Treatment Period 1: During Treatment Period 1, eligible subjects will be randomized (1:1) to one of the following treatment arms: - Arm 1: Active NAL ER followed by crossover Placebo in Treatment Period 2 - Arm 2: Placebo followed by crossover NAL ER in Treatment Period 2 Following 3 weeks of dosing in Treatment Period 1, subjects will complete a 2-week washout period before entering Treatment Period 2. Subjects assigned to Arm 1 will receive placebo and subjects assigned to Arm 2 will receive NAL ER during Treatment Period 2. A final 2-week washout period will occur at the completion of Treatment Period 2. NAL ER Dosing Subjects on NAL ER will have the dose titrated from 27 mg once daily (QD) to 54 mg twice a day (BID) over a 5-day period and then maintained at 54 mg twice a day (BID) for approximately 4 days. Doses will be subsequently escalated and maintained at 108 mg twice a day (BID) over 1 week and then to 162 mg twice a day (BID) over 6 days.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 42
• Est. completion date: May 27, 2022
• Est. primary completion date: May 27, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

1. Individuals diagnosed with Idiopathic Pulmonary Fibrosis

2. Chronic cough > 8 weeks.

3. Daytime cough severity score = 4 on Cough Severity Numerical Rating Scale at screening

Exclusion Criteria:

1. The following conditions are excluded:

1. Interstitial lung disease (ILD) known to be caused by domestic and occupational environmental exposures.

2. Interstitial lung disease (ILD) known to be caused by connective tissue disease.

3. Interstitial lung disease (ILD) known to be caused by drug related toxicity.

2. Currently on continuous oxygen therapy.

3. History of substance abuse that, as determined by the Investigator, may interfere with the conduct of the study

Related Conditions & MeSH terms

• Cough
• Fibrosis
• Idiopathic Pulmonary Fibrosis
• Nalbuphine
• Pulmonary Fibrosis

Intervention

Drug:
• NAL ER
Participants will receive NAL ER 27 mg QD, 27 mg BID, 54 mg BID, 108 mg BID, 162 mg BID over a 3 week period.
• Placebo
Participants will receive Placebo tablet (matching NAL ER BID) over a 3 week period.

Locations

Country	Name	City	State
United Kingdom	11	Antrim	Northern Ireland
United Kingdom	16	Birmingham
United Kingdom	09	Cambridge
United Kingdom	08	Cottingham
United Kingdom	17	Dundee
United Kingdom	13	Edinburgh
United Kingdom	01	London
United Kingdom	04	London
United Kingdom	02	Manchester
United Kingdom	10	Newcastle Upon Tyne
United Kingdom	15	North Shields
United Kingdom	07	Norwich
United Kingdom	06	Nottingham
United Kingdom	14	Oxford
United Kingdom	03	Southampton

Sponsors (2)

Lead Sponsor	Collaborator
Trevi Therapeutics	Parexel

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Comparison of percentage of responders by Treatment	To evaluate the effect of Nalbuphine ER tablets on the mean daytime cough frequency (coughs per hour) at day 22 (dose 162 mg twice daily [BID]) as compared to placebo. Daytime is defined as the period between the time the subject reported being awake and the time the subject went to bed. Assessment is done using objective digital cough monitoring.	Up to 3 weeks
Secondary	Change from baseline daytime cough frequency effect of escalating doses of Nalbuphine ER	To evaluate the effect of escalating doses of Nalbuphine ER on the mean relative change from baseline in daytime cough frequency (coughs per hour) at day 9 (dose: 54 mg BID), day 16 (dose: 108 mg BID) and day 22 (dose: 162 mg BID).	Up to 3 weeks
Secondary	Comparison of percentage of responders on the Evaluating Respiratory Symptoms (E-RS™) diary cough scale	The E-RS will be used to look at the percentage of responders with response defined as at least one category improvement from baseline.	Up to 3 weeks