Two-part Pharmacokinetic and Pharmacodynamic Study of LAS190792 in Patients With Asthma and COPD

• Status: Completed
• Trial end date: 2014-10-06
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this study is to assess the safety and tolerability of single doses of LAS190792 administered by inhalation to patients with mild persistent asthma and moderate to severe chronic obstructive pulmonary disease (COPD) and also to assess the ability of LAS190792 to produce bronchodilation (opening of the airways).

• Phase: Phase 1
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: AstraZeneca
• Treatments: LAS190792; Tiotropium Bromide

Criteria

Inclusion Criteria (PART 1):

• Adult male subjects aged 18 to 70 years

• Body mass index (BMI) 18.5 to 30 kg/m2 at screening

• Clinical diagnosis of mild persistent asthma (according to GINA guidelines) for at least 6 months prior to screening

• Ability to change current asthma therapy, to discontinue previous prescribed medications after signature of informed consent as per required washout periods

• Screening FEV1 value of ≥70% of the predicted normal value after a washout of at least 5 h for short-acting beta2-agonists and 72 h for long-acting beta2-agonists

• FEV1 reversibility of ≥12% and an absolute increase of at least 200 mL over the baseline value within 30 min after inhalation of 400 µg of salbutamol

• Subjects using intermittent salbutamol and / or subjects on a stable dose or regimen of low dose ICS (as defined by the GINA guidelines) at least 4 weeks prior to screening

• Predose FEV1 value of first treatment period within the range of ±20% of the FEV1 measured at screening prior to salbutamol inhalation

• Subjects who are otherwise healthy as determined by medical history, physical examination, 12-lead ECG findings

• Normal blood pressure (defined as SBP between 100 and 140 mmHg, and DBP between 50 and 90 mmHg) at screening, measured after resting in supine position for 5 minutes.

• Subjects whose clinical laboratory test results are not clinically relevant and are acceptable to the Investigator

• Subjects who are negative for hepatitis B surface antigen (HBsAg), hepatitis B core (HBc) antibody (IgM), hepatitis C antibody and human immunodeficiency virus (HIV) I and II antibodies at screening

• Subjects who are able and willing to provide written informed consent

• Subjects able to perform repeatable pulmonary function testing for FEV1 according to the American Thoracic Society (ATS) / European Respiratory Society (ERS) 2005 criteria at screening

Inclusion Criteria (PART 2):

• Adult male and non-childbearing potential women subjects aged ≥40 years with a clinical diagnosis of stable moderate to severe COPD according to GOLD guidelines at screening

• Females must be of non-childbearing potential, confirmed at screening

• Post-salbutamol FEV1 <80% and ≥30% of the predicted normal value and post-salbutamol FEV1 / forced vital capacity (FVC) <70%

• Ability to change current COPD therapy, to discontinue previous prescribed medications after signature of informed consent

• No evidence of clinically significant respiratory and / or cardiovascular conditions or laboratory abnormalities

• No other relevant pulmonary disease or history of thoracic surgery

• No contraindication to the use of anticholinergic drugs such as known symptomatic prostatic hypertrophy, bladder neck obstruction, narrow-angle glaucoma, or beta2-agonists usage

• Subjects who are negative for HBsAg, HBc IgM, hepatitis C antibody and HIV I and II antibodies at screening

• Subjects who are able and willing to provide written informed consent

• Subjects able to perform repeatable pulmonary function testing for FEV1 according to the ATS / ERS 2005 criteria at screening

Exclusion Criteria (PART 1 and 2):

• Subjects who do not conform to the above inclusion criteria

• Current smokers, subjects with a smoking history during the last 12 months or subjects with a smoking history of more than 10 pack-years

• Other relevant pulmonary disease or history of thoracic surgery

• Subjects with a BMI ≥40 kg/m2 (only applicable for Part 2)

• Subjects with any clinically relevant history or presence of abnormality from the medical history and/or physical examination (only applicable for Part 1)

• Current evidence or recent history of any clinically significant and unstable disease (other than COPD) or abnormality that could put the subject at risk or could confound the results of the study (only applicable for Part 2)

• Subjects with a surgical history clinically relevant for the purpose of the study

• History of malignancy of any organ system, treated or untreated within the past 5 years, with the exception of localised basal cell carcinoma of the skin

• Subjects with serious adverse reaction or serious hypersensitivity to Spiriva (for Part 2 only), indacaterol (for Part 2 only), or the formulation excipients (eg, lactose) or other drugs in the same pharmacologic class (for Part 1 and Part 2)

• Current diagnosis of COPD (for Part 1 only) or history of / or current diagnosis for asthma (for Part 2 only)

• Recent history of asthma / COPD exacerbation requiring hospitalisation or need for increased maintenance treatments for asthma / COPD within 6 weeks prior to screening or randomisation

• Use of daily oxygen therapy >10 h per day (for Part 2 only)

• Use of systemic steroids for respiratory reasons within 3 months prior to screening

• Lower respiratory tract infection within 6 weeks prior to screening or randomisation

• Upper respiratory tract infection requiring antibiotics within 4 weeks prior to screening or randomisation

• Current history of tuberculosis, bronchiectasis or other non-specific pulmonary disease

• QTcF interval >430 ms at screening or prior to randomisation, or history of long QT syndrome (for Part 1 only)

• QTcF interval, >450 ms for males and >470 ms for females at screening or prior to randomisation, or history of long QT syndrome (for Part 2 only)

• Subjects with a history of excessive use or abuse of alcohol or with a history of drug abuse within the past 2 years

• Subjects who are positive for drugs of abuse and alcohol tests at screening and prior to randomisation

• Donation or loss >400 ml of blood and plasma within the previous 3 months prior to screening

• Subjects consuming more than 14 (female subjects) or 21 (male subjects) units of alcohol a week

• Subjects with a significant infection or known inflammatory process at screening or prior to randomisation

• Subjects with acute gastrointestinal symptoms at the time of screening or prior to randomisation

• Subjects with an acute infection such as influenza at the time of screening or prior to randomisation

• Male subjects who do not agree to follow instructions to avoid pregnancies

• Subjects who are not able to adhere to the restrictions on prior and concomitant medications

• Subjects who intend to use any concomitant medication not permitted by the protocol or who have not undergone the required washout period for a particular prohibited medication

• Subjects who have used any investigational drug within 3 months prior to screening or within the equivalent time of 6 half-lives of receiving the last administration, whichever is longer

• Subjects who have received the last dose of investigational product more than 3 months ago but who are on an extended follow-up

• Subjects who are vegans or who have medical dietary restrictions

• Subjects unable to communicate reliably with the Investigator

• Subjects who are unlikely to co-operate with the requirements of the study