Assessment of Lung Function After Single Inhalations of a Bronchodilator From 2 Configurations a Dry Powder Inhaler.

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
GlaxoSmithKline
ClinicalTrials.gov Identifier:
NCT01521390
First received: January 26, 2012
Last updated: August 16, 2012
Last verified: August 2012
  Purpose

GSK573719 is a high-affinity specific muscarinic receptor (mAChR) antagonist which is being developed for the treatment of chronic obstructive pulmonary disease (COPD). The long duration of action of GSK573719, when administered via inhalation to humans supports the potential for use as a long acting bronchodilator.This is a randomized, double-blind, placebo-controlled, 5 period cross-over study in healthy male and female volunteers. The study will measure lung function after single inhaled doses from two configurations of the Novel Dry Powder Inhaler. Key assessments will include clinical relevant PD parameters: sGaw, FEV1


Condition Intervention Phase
Pulmonary Disease, Chronic Obstructive
Drug: GSK573719 62.5 mcg (one strip)
Drug: GSK573719 62.5 mcg(two strips)
Drug: GSK573719 125 mcg (one strip)
Drug: GSK573719 125 mcg(two strips)
Drug: Placebo
Phase 1

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Pharmacodynamics Study
Intervention Model: Crossover Assignment
Masking: Double Blind (Subject, Investigator, Outcomes Assessor)
Official Title: Randomized, Double-blind, 5 Period Cross Over Study Assessing Lung Function in Healthy Volunteers Following Single Inhalations of GSK573719 Inhalation Powder From Two Configurations of the Novel Dry Powder Inhaler

Resource links provided by NLM:


Further study details as provided by GlaxoSmithKline:

Primary Outcome Measures:
  • Weighted mean and maximal change from baseline in sGaw [ Time Frame: serial over 24 hr for each treatment period ] [ Designated as safety issue: No ]
    measured by plethysmography, for each inhaled dose from one strip configuration as compared with two strip


Secondary Outcome Measures:
  • Plasma concentration of GSK573714 [ Time Frame: over 24 hrs for each treatment period ] [ Designated as safety issue: No ]
    Pharmacokinetic parameters

  • Urine concentration of GSK573714 [ Time Frame: over 24 hr for each treatment period ] [ Designated as safety issue: No ]
    Pharmacokinetic parameters

  • Blood pressure [ Time Frame: over 24 hr for each treatment period ] [ Designated as safety issue: Yes ]
  • Heart Rate [ Time Frame: over 24 hr for each treatment period ] [ Designated as safety issue: Yes ]
  • Serial FEV1 [ Time Frame: over 24 hr ] [ Designated as safety issue: No ]
  • Serial sGaw [ Time Frame: over 24 hr for each treatment period ] [ Designated as safety issue: No ]
  • ECG [ Time Frame: over 24 hrs for each treatment period ] [ Designated as safety issue: Yes ]
    12-lead ECG

  • Clinical lab safety tests [ Time Frame: Over 24 hrs for each treatment period ] [ Designated as safety issue: Yes ]
    Haematology, Biochemistry and Urinalysis


Enrollment: 15
Study Start Date: October 2011
Study Completion Date: December 2011
Primary Completion Date: December 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Treatment Arm
Subjects receive one inhalation from each intervention
Drug: GSK573719 62.5 mcg (one strip)
GSK573719 62.5 mcg delivered by 1 strip configuration of novel dry powder inhaler
Drug: GSK573719 62.5 mcg(two strips)
GSK573719 62.5 mcg delivered by 2 strip configuration of novel dry powder inhaler
Drug: GSK573719 125 mcg (one strip)
GSK573719 125 mcg delivered by 1 strip configuration of novel dry powder inhaler
Drug: GSK573719 125 mcg(two strips)
GSK573719 125 mcg delivered by 2 strip configuration of novel dry powder inhaler
Drug: Placebo
Placebo, no active ingredient

  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Male or female between 18 and 65 years of age inclusive, at the time of signing the informed consent.
  • Healthy male or female as determined by a responsible and experienced physician, based on a medical evaluation including [medical history, physical examination, laboratory tests and cardiac monitoring]. A subject with a clinical significant abnormality or laboratory parameters outside the reference range for the population being studied may be included only if the Investigator believes that the finding is unlikely to introduce additional risk factors and will not interfere with the study procedures.
  • A female subject is eligible to participate if she is of:

    • Non-childbearing potential defined as pre-menopausal females with a documented tubal ligation or hysterectomy; or postmenopausal defined as 12 months of spontaneous amenorrhea [in questionable cases a blood sample with simultaneous follicle stimulating hormone (FSH) > 40 MlU/ml and estradiol < 40 pg/ml (<147 pmol/L) is confirmatory]. [Females on hormone replacement therapy (HRT) and whose menopausal status is in doubt will be required to use one of the contraception methods in Section 8.1 if they wish to continue their HRT during the study. Otherwise, they must discontinue HRT to allow confirmation of post-menopausal status prior to study enrollment. For most forms of HRT, at least 2-4 weeks will elapse between the cessation of therapy and the blood draw; this interval depends on the type and dosage of HRT. Following confirmation of their post-menopausal status, they can resume use of HRT during the study without use of a contraceptive method.]
    • Child-bearing potential and agrees to use one of the contraception methods listed in Section 8.1 for an appropriate period of time (as determined by the product label or investigator) prior to the start of dosing to sufficiently minimize the risk of pregnancy at that point. Female subjects must agree to use contraception until 10 days after last dose.
  • Body weight ≥ 50 kg and BMI within the range 19.0 - 29.9 kg/m2 (inclusive).
  • Normal spirometry (FEV1 ≥ 80% of predicted, FEV1/FVC ≥ 70%).
  • Response to ipratropium bromide defined as

    • an increase in sGaw of ≥25% over pre-dose baseline at 2 h following 80μg ipratropium bromide; or
    • a documented increase in sGaw of ≥25% over pre-dose baseline at 2 h following inhalation of 80 μg of ipratropium bromide within 3 months of screening.
  • AST, ALT, alkaline phosphatase and bilirubin ≤ 1.5xULN (isolated bilirubin >1.5xULN is acceptable if bilirubin is fractionated and direct bilirubin <35%).
  • No significant abnormality on 12-lead ECG at screening, including QTcF < 450msec.
  • Non-smokers (never smoked or not smoking for >6 months with <10 pack years history (Pack years = (cigarettes per day smoked/20) x number of years smoked))
  • Subjects who are able to use the Novel DPI satisfactorily
  • Subjects, who are capable of giving written informed consent, have signed and dated the informed consent form which includes compliance with the requirements and restrictions listed in the consent form.

Exclusion Criteria:

  • A supine mean heart rate outside the range 40-90 beats per minute (BPM) at screening.
  • A supine blood pressure that is persistently higher than 140/90 millimetres of mercury (mmHG) at screening.
  • History of symptomatic arrhythmias.
  • A positive pre-study Hepatitis B surface antigen or positive Hepatitis C antibody result within 3 months of screening
  • Current or chronic history of liver disease, or known hepatic or biliary abnormalities (with the exception of Gilbert's syndrome or asymptomatic gallstones).
  • A positive pre-study drug/alcohol screen.
  • A positive test for HIV antibody.
  • History of regular alcohol consumption within 6 months of the study defined as:

    • an average weekly intake of >21 units for males or >14 units for females. One unit is equivalent to 8 g of alcohol: a half-pint (~240 ml) of beer, 1 glass (125 ml) of wine or 1 (25 ml) measure of spirits.

  • The subject has participated in a clinical trial and has received an investigational product within the following time period prior to the first dosing day in the current study: 30 days, 5 half-lives or twice the duration of the biological effect of the investigational product (whichever is longer).
  • Exposure to more than four new chemical entities within 12 months prior to the first dosing day.
  • Use of prescription or non-prescription drugs, including vitamins, herbal and dietary supplements (including St John's Wort) within 7 days (or 14 days if the drug is a potential enzyme inducer) or 5 half-lives (whichever is longer) prior to the first dose of study medication, unless in the opinion of the Investigator and GSK Medical Monitor the medication will not interfere with the study procedures or compromise subject safety.
  • History of sensitivity to any of the study medications, or components thereof or a history of drug or other allergy that, in the opinion of the Investigator or GSK Medical Monitor, contraindicates their participation.
  • Where participation in the study would result in donation of blood or blood products in excess of 500 mL within a 56 day period.
  • Pregnant females as determined by positive serum or urine hCG test at screening or prior to dosing.
  • Lactating females.
  • Unwillingness or inability to follow the procedures outlined in the protocol.
  • Subject is mentally or legally incapacitated.
  • Subject who has asthma or a history of asthma or bronchoconstriction.
  • Urinary cotinine levels indicative of smoking or history or regular use of tobacco or nicotine-containing products within 6 months prior to screening.
  • Subjects who are kept due to regulatory or juridical order in an institution.
  • Subjects who are in military service.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01521390

Locations
Germany
GSK Investigational Site
Berlin, Germany, 14050
Sponsors and Collaborators
GlaxoSmithKline
Investigators
Study Director: GSK Clinical Trials GlaxoSmithKline
  More Information

No publications provided

Responsible Party: GlaxoSmithKline
ClinicalTrials.gov Identifier: NCT01521390     History of Changes
Other Study ID Numbers: 115487
Study First Received: January 26, 2012
Last Updated: August 16, 2012
Health Authority: United States: Food and Drug Administration
Germany: Bundesinstitut für Arzneimittel und Medizinprodukte

Additional relevant MeSH terms:
Respiratory Aspiration
Chronic Disease
Lung Diseases
Pulmonary Disease, Chronic Obstructive
Respiration Disorders
Respiratory Tract Diseases
Pathologic Processes
Disease Attributes
Lung Diseases, Obstructive

ClinicalTrials.gov processed this record on August 01, 2014