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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
Vernalis (R&D) Ltd
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cough focused on measuring Chronic Cough, Indantadol

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

First Posted
July 21, 2011
Last Updated
July 22, 2011
Sponsor
Vernalis (R&D) Ltd
Collaborators
Manchester University NHS Foundation Trust
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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

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Phase II Open-Label Pilot Study of V3381 in Chronic Cough

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