Effects of Salmeterol on Autonomic Nervous System

• Status: Completed
• Trial end date: 2012-11-01
• Target enrollment: 0
• Participant gender: All

Summary

This is a 4-week non-randomized, partially blinded, single-arm monocentre study in subjects with Chronic Obstructive Pulmonary Disease (COPD) Global Initiative for Chronic Obstructive Lung Disease (GOLD) class II or III with the aim to demonstrate that inhaled therapy with salmeterol reduces sympathetic activity as evaluated by microneurography. A maximum of 32 subjects is planned to be enrolled.

• Phase: Phase 4
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: GlaxoSmithKline
• Treatments: Salmeterol Xinafoate

Criteria

Inclusion Criteria:

• COPD of GOLD Class II or III with a post-bronchodilator spirometry forced expiratory volume in one second (FEV1) <60% predicted and FEV1/vital capacity (VC) <70% in accordance with the GOLD executive summary

• Subject is ambulatory (outpatient)

• Subject is therapy-naive (defined as not receiving any previous regular COPD therapy)

• Subjects with a current or prior history of ≥10 pack-years of cigarette smoking at Screening Visit. Previous smokers are defined as those who have stopped smoking for at least 1 month prior to Visit 1

• Willing to participate in the study, must be able to inhale study medication

Exclusion Criteria:

• Women who are pregnant or lactating

• Subjects not willing or unable to sign the informed consent before study start

• diagnosis of asthma

• α-1 antitrypsin deficiency

• active tuberculosis, lung cancer, bronchiectasis, sarcoidosis, lung fibrosis, pulmonary hypertension, interstitial lung diseases or other active pulmonary diseases

• Subjects with lung volume reduction surgery within the 12 months prior to Screening

• Subjects who have been hospitalized due to poorly controlled COPD within 6 weeks prior to the Screening Visit

• Subjects with poorly controlled COPD, defined as the occurrence of an exacerbation managed with systemic corticosteroids or antibiotics prescribed by a physician 6 weeks prior to the Screening Visit

• Frequent exacerbations necessitating the therapy with inhaled glucocorticosteroids according to the GOLD guideline

• COPD with nasal intermittent positive pressure ventilation (NIPPV)

• Treatment with drugs having direct sympathomimetic activity (e.g. theophylline, moxonidine, clonidine), Oral medication with beta2-sympathomimetics

• Inhaled therapy with anti-cholinergics, sodium cromoglycate or nedocromil sodium

• Treatment with systemic, oral or parenteral (intra-articular) corticosteroids

• Treatment with strong cytochrome P450 3A4 inhibitors

• Treatment with any other investigational drug

• Oxygen therapy: Subjects receiving treatment with long-term oxygen therapy (LTOT) or nocturnal oxygen therapy required for greater than 12 hours a day

• Subjects who are medically unable to withhold their short-acting beta-agonist (SABA) for the 6-hour period required prior to spirometry testing at each study visit

• Subjects with clinically significant sleep apnoea that is uncontrolled

• Unstable angina pectoris or signs and history of left heart failure with a left ventricular ejection fraction <40%

• Arterial hypertension necessitating treatment with >1 antihypertensive drug

• Clinically evident polyneuropathy

• Diabetes mellitus necessitating any pharmacological therapy

• Severe concomitant disease (likely to reduce life expectancy to less than 3 years)

• Other diseases/abnormalities: Subjects with historical or current evidence of clinically significant neurological, psychiatric, renal, hepatic, immunological, endocrine or haematological abnormality that is uncontrolled