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Treatment With AKL1 in Obstructive Airways Disease (The TAKL Study) (TAKL)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00920127
Recruitment Status : Unknown
Verified August 2011 by University of East Anglia.
Recruitment status was:  Active, not recruiting
First Posted : June 15, 2009
Last Update Posted : August 5, 2011
Information provided by:
University of East Anglia

Brief Summary:

Obstructive airways disease is a very common condition. This condition includes patients with asthma, chronic obstructive pulmonary disease (COPD), emphysema or chronic bronchitis. Some patients with obstructive airways disease have problems with long term breathlessness, wheeze and cough with or without sputum production. Currently the researchers give treatments - usually inhalers - which are designed to open the airways and reduce the breathlessness and wheeze. Despite these available treatments many patients still have continuing symptoms.

Anecdotal clinical evidence suggested that a herbal remedy (called AKL1) has beneficial effects in respiratory conditions, with patients diagnosed as having both asthma and COPD reporting reduced symptoms including breathlessness and cough and reduced frequency of attacks.The purpose of this study is to confirm whether AKL1 does indeed have a meaningful benefit to patients with obstructive airways disease. The researchers will mainly be measuring any effect of AKL by assessing any change in trial subjects' coughs, using a questionnaire, but the researchers will also looking at breathing tests, walking tests, blood and sputum tests.

Condition or disease Intervention/treatment Phase
Obstructive Lung Disease Chronic Obstructive Pulmonary Disease Asthma Dietary Supplement: AKL1 Phase 2 Phase 3

Detailed Description:

The outcomes of care for obstructive airways disease in the UK and other countries fail to meet guideline targets, with high levels of avoidable morbidity and avoidable mortality. Obstructive lung disease is an encompassing term for a condition that includes patients with a reversible (asthma) or non reversible (chronic obstructive pulmonary disease) component to their lung function.

AKL1 is a novel pharmaceutical agent derived from a combination of botanical products developed as a treatment for obstructive lung disease (asthma and COPD). The botanical product contains a synthetically-derived phytochemical component of Picrorrhiza kurroa, apocynin, together with standardized extracts of Picrorrhiza kurroa, Zingiber officinale and Ginkgo biloba that have previously been marketed as a health food supplements. Recent evidence suggests that Ginkgo biloba reduces inflammatory (protein kinase C positive ie eosinophils and neutrophils) cells in induced sputum which given in addition to inhaled corticosteroids to asthmatic patients. Anecdotal clinical evidence suggests that the botanical product has significant activity in respiratory conditions, with patients diagnosed as having obstructive lung disease (asthma and COPD) reporting reduced symptoms including breathlessness and cough, reduced frequency of attacks, reduced dependence on bronchodilators and ability to reduce inhaled corticosteroids dose.

We have completed a pilot study investigating the efficacy and safety of AKL1 as 'add-on' therapy for adult patients diagnosed as having obstructive lung disease whose symptoms remained uncontrolled on standard medication. Whilst there was no significant differences in lung function, there were trends to clinical improvements in the patient-centered outcomes e.g. cough, health status and exacerbation frequency. Hence a larger adequately powered study is needed to investigate these outcomes further.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 164 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: An Investigation of the Safety and Efficacy of Oral AKL1 in Patients Diagnosed With Obstructive Lung Disease
Study Start Date : June 2009
Actual Primary Completion Date : February 2011
Estimated Study Completion Date : February 2012

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Lung Diseases

Arm Intervention/treatment
Placebo Comparator: Placebo Dietary Supplement: AKL1

Each dose of AKL1 or placebo will consist of two capsules which will be swallowed twice daily for 8 weeks.

The morning dose of study medication should be taken at approximately the same time each morning between 7:00 am and 10:00 am and should consist of two 500 mg capsules and then repeated between 7.00 pm and 10 pm.

Active Comparator: AKL1 Dietary Supplement: AKL1

Each dose of AKL1 or placebo will consist of two capsules which will be swallowed twice daily for 8 weeks.

The morning dose of study medication should be taken at approximately the same time each morning between 7:00 am and 10:00 am and should consist of two 500 mg capsules and then repeated between 7.00 pm and 10 pm.

Primary Outcome Measures :
  1. The change in the Leicester Cough Questionnaire (LCQ) score [ Time Frame: 8 weeks ]

Secondary Outcome Measures :
  1. St Georges Respiratory Questionnaire (SGRQ) score [ Time Frame: 8 weeks ]
  2. EQ-5D score [ Time Frame: 8 weeks ]
  3. Spirometry (FEV1, FVC, PEF, FEF25-75 predicted) [ Time Frame: 8 weeks ]
  4. Impulse Oscillometry [ Time Frame: 8 weeks ]
  5. Differential spontaneous sputum cell count; TNFα,IL-8, IL-10 concentration [ Time Frame: 8 weeks ]
  6. Modified MRC dyspnoea score [ Time Frame: 8 weeks ]
  7. 6 minute walk [ Time Frame: 8 weeks ]
  8. Blood haematology and biochemistry [ Time Frame: 10 weeks ]
  9. Drug related adverse events [ Time Frame: 10 weeks ]

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 80 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Males or females, aged between 18 to 80 years, inclusive
  • The patient has received verbal and written study information, all questions have been answered satisfactorily and a consent form has been personally signed and dated by the patient and the investigator
  • A diagnosis of obstructive lung disease (with reference to the - International Primary Care Respiratory Group (IPCRG) Guidelines)(4). This being evidenced as a post bronchodilator ratio of FEV1/FVC < 0.7 at Visit 1 or 2 The patient has a post bronchodilator FEV1 of greater than 40% and less than 80% at Visit 1 or 2
  • Patients have a history of regular sputum production (> 3 days per week)
  • LCQ score of <17 (higher score indicates improvement).
  • A MRC dyspnoea score of 3 or more
  • Females must be post menopausal (> 1 year), surgically sterilised or using adequate hormonal contraception, intrauterine device), not breast feeding and have a negative serum pregnancy test
  • The patient must have a satisfactory health with the exception of obstructive lung disease as determined by the investigator on the basis of medical history and physical examination
  • In the Investigator's judgement, the patient is able and willing to comply with study visits and procedures (including laboratory tests, lung function tests).
  • Subjects must be able to demonstrate ability to use salbutamol MDI during the screening period

Exclusion Criteria:

  • The patient has currently poorly controlled disease defined as requiring a course of oral or parenteral corticosteroids or an exacerbation of their obstructive lung disease in the three months prior to Visit 2.
  • The patient has had a recent change in maintenance therapy (i.e. within 6 weeks)
  • Maintenance oral corticosteroid treatment or use of unlicensed doses of inhaled corticosteroid medication (>2000mcg beclomethasone diproprionate/ day or equivalent)
  • The patient has seasonal disease alone
  • The patient has any known laboratory abnormality, which in the opinion of the investigator, would contraindicate study participation, including, aspartate aminotransferase (AST) or alanine aminotransferase (ALT)greater/equal to 1.5 x upper limit of normal (ULN) or creatinine > 1.5 mg/dL
  • The patient is unable to discontinue short-acting beta-2-adrenergic agonists for at least 4 hours, long-acting beta agonists (12 hours) and tiotropium (24 hours) prior to Visit 2 (Week 0)
  • The patient has chronic heart failure class III or IV (New York Heart Association) or a recent (less than six months) history of stroke, transient ischemic attack or myocardial infarction
  • The patient is not able to follow study procedures (e.g., language problems, psychological disorders) or is considered to be non-compliant according to the investigator.
  • The patient has a history of known alcohol or substance abuse (excluding cigarettes) within the one-year prior to Visit 1
  • The patient has an active malignancy of any type or history of a malignancy (with the exception of patients with malignancy surgically removed with no evidence of recurrence within five years before enrolment, and patients with history of treated basal cell carcinoma)
  • The patient has any other severe or acute or chronic medical or psychiatric conditions that may increase the risk associated with study participation or study drug administration or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the patient inappropriate for entry into this study. Subjects with a malignancy and who are currently undergoing radiation therapy or have had chemotherapy within 5 years.
  • The patient has difficulty swallowing capsules or tablets, dysphagia or is unable to tolerate oral medication
  • The patient has been previously admitted to the study or currently participating or have recently participated in another trial with an investigational drug within 90 days of the start of this study.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00920127

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United Kingdom
University of East Anglia
Norwich, Norfolk, United Kingdom, NR47TJ
Sponsors and Collaborators
University of East Anglia
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Principal Investigator: Andrew Wilson, MD, MRCP (UK) University of East Anglia

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Responsible Party: Dr Andrew M Wilson, University of East Anglia Identifier: NCT00920127    
Other Study ID Numbers: 32227/0001/001
EudraCT: 2222 - 222222-22
First Posted: June 15, 2009    Key Record Dates
Last Update Posted: August 5, 2011
Last Verified: August 2011
Keywords provided by University of East Anglia:
Additional relevant MeSH terms:
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Lung Diseases
Lung Diseases, Obstructive
Pulmonary Disease, Chronic Obstructive
Respiratory Tract Diseases