Study of the Safety and Effectiveness of BC1036 Capsules to Treat Frequent Long-Term Cough

Cough Clinical Trial

Official title:

A Multicentre, Double-Blind, Placebo-Controlled, Adaptive Pivotal Study of the Efficacy and Safety of Oral BC1036 in the Management of Cough

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01656668
• Other study ID #: BC1036-001
• Status: Completed
• Phase: Phase 3
• First received: July 27, 2012
• Last updated: August 1, 2013
• Start date: July 2012
• Est. completion date: August 2013

Study information

• Verified date: August 2013
• Source: Respicopea Limited
• Contact: n/a
• Is FDA regulated: No
• Health authority: United Kingdom: Medicines and Healthcare Products Regulatory Agency
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to investigate the effect of BC1036 (theobromine) on cough-related quality of life and cough severity following 2 weeks' treatment.

Description:

Cough is a common and disabling symptom. At any one time 20% of the population have a troublesome cough and sufferers consume 75 million doses of over-the-counter anti-tussive (anti-cough) medication annually. Chronic cough can be the presenting symptom of almost all respiratory conditions; it can also occur in the absence of overt lung pathology. The only study to grade cough severity found 7% of a general population had cough sufficient to interfere with activities of daily living on at least a weekly basis in the UK. Cross sectional studies have consistently shown that chronic cough is particularly prevalent in middle aged females.

The investigational medicinal product BC1036 (theobromine) is being developed as a non-codeine, non-narcotic treatment for persistent cough. Theobromine is a well characterised molecule with a long history of safe use both as a medicine and as a food product. As a member of the xanthine family, it bears structural and pharmacological similarity to caffeine and theophylline, both of which have long been approved for medicinal use.

This is a placebo-controlled, double-blind, parallel group study of BC1036 in subjects with persistent cough (chronic or sub-acute), treatment resistant after a routine clinical assessment as outlined in the BTS Recommendations for the Management of Cough in Adults and despite adequate treatment of any associated potential aggravating factors or without the continuance of any obvious precipitating factors. The objective is to investigate the effect of BC1036 on cough-related quality of life and cough severity following 2 weeks' treatment. It is planned to recruit 288 evaluable subjects from cough clinics, secondary and primary care centres in the UK. Subjects will receive either BC1036 or placebo over a period of 14 days.

Eligible subjects will be required to attend the clinic on five occasions: screening, baseline, days 7, 14, and a follow up visit at day 28. At every visit the subjects will complete the Leicester Cough Questionnaire (LCQ), and a cough Visual Analogue Score (VAS). Spirometry will be performed for measurement of lung function. Blood samples will be drawn for safety clinical laboratory parameters and physical examinations and ECG will be performed. Subjects should be seen for all visits on the designated day ± 1 day, except Day 28 ± 2 days.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 288
• Est. completion date: August 2013
• Est. primary completion date: August 2013
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Male or female aged 18 to 75 years.

• Confirmed diagnosis of a persistent cough.

• Leicester Cough Questionnaire score of = 17 at baseline.

• FEV = 70% of predicted normal, at screening. See protocol Appendix 4 for formula for calculating predicted values.

• Willing to use effective contraception for the duration of the study. Female subjects who are neither surgically sterilized nor post-menopausal (defined as no menses for one year or an FSH value > 40 mIU/L) will be required to use two methods throughout the study and for 30 days after. Besides abstinence the following contraceptive methods are acceptable: hormonal (e.g. oral, injection, transdermal patch, implant, cervical ring), barrier (e.g. condom or diaphragm with spermicidal agent) or intrauterine device. If hormonal contraceptives are used they must be used from 6 weeks before the first administration of test product. Male subjects must agree to use condoms for the duration of the study and for 30 days after.

• Willing and able to give informed consent and of complying with the trial assessments and any other trial procedures.

Exclusion Criteria:

• Pregnant or lactating females.

• Major surgery within the 30 days preceding the screening visit.

• Any serious infections within the 30 days prior to the screening visit.

• Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, uncontrolled diabetes, renal or hepatic disease or psychiatric illness/social situations that would limit compliance with study requirements.

• Known hepatitis B or C or human immunodeficiency virus (HIV) or syphilis seropositivity.

• A history of serious adverse allergic reaction to any medication.

• Treatment with another investigational medicinal product within the 30 days prior to enrollment.

• Treatment with:

• Systemic oral steroids within 7 days prior to randomisation at Visit 2.

• Theophylline and theophylline-like agents within 7 days prior to randomisation.

• Opiates or opioids e.g. codeine, dextromethorphan, within 7 days prior to randomisation.

• ACE inhibitors within one month prior to the screening visit.

• Depot injection of corticosteroids within 6 weeks of the screening visit.

• History suggestive of febrile illness within the last 7 days prior to the screening visit.

• Subjects with significant sputum production (defined as more than 5 ml (~one teaspoon)/day on any three days in the screening period).

• Current smokers or past smokers who have a smoking history of > 20 pack years or stopped smoking = 12 months prior to screening.

• Any pulmonary co-morbidity such as COPD, recurrent lower respiratory tract infections (= 2 in the 12 months prior to screening) and bronchiectasis where cough suppression may lead to sputum retention and infection.

• Any pulmonary abnormality on chest X-ray or CT scan performed in the twelve months prior to enrolment indicative of COPD, bronchiectasis etc.

• Subjects diagnosed with asthma who have suffered an exacerbation requiring hospitalisation within 4 weeks prior to screening.

• A history of cancer within the previous five years (excluding carcinoma in situ or nonmelanoma skin cancer treated by surgical excision).

• Uncontrolled hypertension (resting systolic BP > 170mmHg or resting diastolic BP > 95 mm Hg).

• A corrected QT interval of > 470ms for female subjects or of > 450ms for male subjects, calculated using the QTcF correction formula, or second degree or higher heart block on an ECG recording, at screening.

• Subjects known to have a sensitivity to methylxanthines and related compounds, or known to have exhibited an allergic response or sensitivity to cocoa-based products.

• History or presence of alcohol or substance abuse.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Cough

Intervention

Drug:
• BC1036

Locations

Country	Name	City	State
United Kingdom	Ormeau Road Health Centre	Belfast
United Kingdom	The Queen's University of Belfast	Belfast
United Kingdom	Castle Hill Hospital	Cottingham
United Kingdom	The Medical Centre	East Horsely
United Kingdom	Sheepcot Medical Centre	Garston, Watford
United Kingdom	Glenfield Hospital	Leicester
United Kingdom	King's College Hospital	London
United Kingdom	Royal Brompton Hospital	London
United Kingdom	Mortimer Surgery	Mortimer
United Kingdom	Freeman Hospital	Newcastle upon Tyne
United Kingdom	Ecclesfield Group Practice	Sheffield
United Kingdom	Staploe Medical Centre	Soham, Ely
United Kingdom	Albany House Medical Centre	Wellingborough, Northampton

Sponsors (1)

Lead Sponsor	Collaborator
Respicopea Limited

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Pulmonary function tests	Pulmonary function will be measured at all visits using a calibrated spirometer. This includes Forced Expiratory Volume (FEV), Forced Vital Capacity (FVC) and peak flow.	From screening to day 28	No
Primary	Leicester Cough Questionnaire (LCQ)	Cough-related quality of life assessed using the Leicester Cough Questionnaire (LCQ). The baseline-adjusted total LCQ score at Day 14 will be used as the primary endpoint.	Day 14	No
Secondary	Adapted 7-day Leicester Cough Questionnaire (LCQ)	Adapted 7-day LCQ to measure quality of life over the previous 7 days.	Day 7	No
Secondary	Leicester Cough Questionnaire (LCQ)	LCQ at Day 28 will measure quality of life over the previous 14 days.	Day 28	No
Secondary	Cough visual analogue scale (VAS)	VAS scores on a 100 mm scale fixed at both ends by 'no cough' and 'worst cough ever'. Assessment made at every visit.	From screening to Day 28	No
Secondary	Airway sensitivity using capsaicin challenge	Subgroup of approximately 100 subjects will be challenged with capsaicin at Day 0 and Day 14.	Day 0 and Day 14	No