Phase II Open-Label Pilot Study of V3381 in Chronic Cough
Primary Purpose
Cough
Status
Terminated
Phase
Phase 2
Locations
United Kingdom
Study Type
Interventional
Intervention
Indantadol
Sponsored by
About this trial
This is an interventional treatment trial for Cough focused on measuring Chronic Cough, Indantadol
Eligibility Criteria
Inclusion Criteria:
- Male or female 18-75 years of age
- Females must be of non child-bearing potential
- Chronic Cough ( > 8 weeks)
- Normal Chest X-ray
- Normal Lung Function
- Idiopathic or treatment resistant cough-
Exclusion Criteria:
- Recent upper respiratory tract infection (<4 weeks)
- Pregnancy/breast-feeding
- Current smokers or ex-smokers with <6 months abstinence or cumulative history of >10 pack years
- Current treatment with ACE inhibitors.
- Drug or alcohol abuse
- Uncontrolled hypertension (i.e., >140/90 mmHg despite adequate medical therapy).
- Any cardiovascular condition that would be a contra-indication to the use of sympathomimetic amines (e.g. active angina).
- Any clinically significant neurological disorder
- Prior renal transplant, current renal dialysis.
- Any clinically significant or unstable medical or psychiatric condition that would interfere with the patient's ability to participate in the study.
- Increased risk of seizures.
- Any malignancy in the past 2 years (with the exception of basal cell carcinoma).
- Use of opioids, anticonvulsants, antidepressants (particularly MAO inhibitors).
- Any clinically significant abnormal laboratory test result(s).
- Serum creatinine laboratory value greater than 1.5 x upper limit of normal (ULN) reference range (after adjustment for age) or estimated creatinine clearance <60 mL/min.
- Total bilirubin greater than upper limit of normal reference range (with the exception of Gilbert's Syndrome) and/or alanine transaminase (ALT) >1.5 times upper limit of normal reference ranges (after adjustment for age).
Sites / Locations
- South Manchester University Hospital
Outcomes
Primary Outcome Measures
Objective cough frequency at 8 weeks compared to baseline.
Secondary Outcome Measures
Change in objective cough frequency at 4 weeks.
Change in Cough-Specific Quality-of-Life Questionnaire (CQLQ) at 4 and 8 weeks.
Change in Global Rating of Change Scale at 1 week, 2 weeks, 4 weeks and 8 weeks
Full Information
NCT ID
NCT01401673
First Posted
July 21, 2011
Last Updated
July 22, 2011
Sponsor
Vernalis (R&D) Ltd
Collaborators
Manchester University NHS Foundation Trust
1. Study Identification
Unique Protocol Identification Number
NCT01401673
Brief Title
Phase II Open-Label Pilot Study of V3381 in Chronic Cough
Official Title
Phase II Open-label Pilot Study of V3381, a Novel N-Methyl-D-Aspartate Receptor Antagonist, in Chronic Cough Patients Attending a Specialist Clinic
Study Type
Interventional
2. Study Status
Record Verification Date
July 2011
Overall Recruitment Status
Terminated
Why Stopped
Lack of efficacy
Study Start Date
October 2009 (undefined)
Primary Completion Date
August 2010 (Actual)
Study Completion Date
August 2010 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Vernalis (R&D) Ltd
Collaborators
Manchester University NHS Foundation Trust
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The investigators hypothesise that cough reflex hypersensitivity, demonstrated in chronic cough patients, is due to a phenomenon known as central sensitisation. Central sensitisation is a hyper-excitability of the sensory nerves as they join the central nervous system, and is believed to be mediated by the N-Methyl-D-Aspartate (NMDA) receptor[1-3].
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cough
Keywords
Chronic Cough, Indantadol
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
12 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
Indantadol
Intervention Description
Titration
Primary Outcome Measure Information:
Title
Objective cough frequency at 8 weeks compared to baseline.
Time Frame
8 Weeks
Secondary Outcome Measure Information:
Title
Change in objective cough frequency at 4 weeks.
Time Frame
4 Weeks
Title
Change in Cough-Specific Quality-of-Life Questionnaire (CQLQ) at 4 and 8 weeks.
Time Frame
4 and 8 Weeks
Title
Change in Global Rating of Change Scale at 1 week, 2 weeks, 4 weeks and 8 weeks
Time Frame
1 Week, 2 Weeks, 4 Weeks and 8 Weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Male or female 18-75 years of age
Females must be of non child-bearing potential
Chronic Cough ( > 8 weeks)
Normal Chest X-ray
Normal Lung Function
Idiopathic or treatment resistant cough-
Exclusion Criteria:
Recent upper respiratory tract infection (<4 weeks)
Pregnancy/breast-feeding
Current smokers or ex-smokers with <6 months abstinence or cumulative history of >10 pack years
Current treatment with ACE inhibitors.
Drug or alcohol abuse
Uncontrolled hypertension (i.e., >140/90 mmHg despite adequate medical therapy).
Any cardiovascular condition that would be a contra-indication to the use of sympathomimetic amines (e.g. active angina).
Any clinically significant neurological disorder
Prior renal transplant, current renal dialysis.
Any clinically significant or unstable medical or psychiatric condition that would interfere with the patient's ability to participate in the study.
Increased risk of seizures.
Any malignancy in the past 2 years (with the exception of basal cell carcinoma).
Use of opioids, anticonvulsants, antidepressants (particularly MAO inhibitors).
Any clinically significant abnormal laboratory test result(s).
Serum creatinine laboratory value greater than 1.5 x upper limit of normal (ULN) reference range (after adjustment for age) or estimated creatinine clearance <60 mL/min.
Total bilirubin greater than upper limit of normal reference range (with the exception of Gilbert's Syndrome) and/or alanine transaminase (ALT) >1.5 times upper limit of normal reference ranges (after adjustment for age).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ashley Woodcock, Prof.
Organizational Affiliation
South Manchester University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
South Manchester University Hospital
City
Manchester
ZIP/Postal Code
M23 9LT
Country
United Kingdom
12. IPD Sharing Statement
Learn more about this trial
Phase II Open-Label Pilot Study of V3381 in Chronic Cough
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