Batefenterol/Fluticasone Furoate in Treatment of Chronic Obstructive Pulmonary Disease

Inclusion Criteria:

- Type of subject: Outpatient.

- Informed Consent: Capable of giving signed informed consent, which includes
compliance with pre-specified requirements and restrictions.

- Age and gender: Male and female subjects, 40 years of age or older at the time of
signing the informed consent, are eligible to participate in the study.

Female subject: is eligible to participate if she is not pregnant (as confirmed by a
negative urine human chorionic gonadotrophin (hCG) test), not lactating, and at least one
of the following conditions applies:

1. Non-reproductive potential defined as:

Pre-menopausal females with one of the following: documented tubal ligation;
documented hysteroscopic tubal occlusion procedure with follow-up confirmation of
bilateral tubal occlusion; hysterectomy; documented bilateral oophorectomy
Postmenopausal defined as 12 months of spontaneous amenorrhea. Females on hormone
replacement therapy (HRT) and whose menopausal status is in doubt will be required to
use one of the highly effective contraception methods 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 enrolment.

2. Reproductive potential and agrees to follow one of the options listed below 30 days
prior to the first dose of study medication and until at least five terminal
half-lives OR until any continuing pharmacologic effect has ended, whichever is
longer after the last dose of study medication and completion of the follow-up visit.
This list does not apply to females of reproductive potential with same sex partners,
when this is their preferred and usual lifestyle or for subjects who are and will
continue to be abstinent from penile-vaginal intercourse on a long term and
persistent basis:

Contraceptive subdermal implant that meets the standard operating procedure (SOP)
effectiveness criteria including a <1% rate of failure per year, as stated in the product
label Intrauterine device or intrauterine system that meets the SOP effectiveness criteria
including a <1% rate of failure per year, as stated in the product label Oral
Contraceptive, either combined or progestogen alone Injectable progestogen Contraceptive
vaginal ring Percutaneous contraceptive patches Male partner sterilization with
documentation of azoospermia prior to the female subject's entry into the study, and this
male is the sole partner for that subject These allowed methods of contraception are only
effective when used consistently, correctly and in accordance with the product label. The
investigator is responsible for ensuring that subjects understand how to properly use
these methods of contraception.

- Chronic Obstructive Pulmonary Disease (COPD): An established clinical history of COPD
in accordance with the definition by the American Thoracic Society/European
Respiratory Society.

- COPD Disease severity: A post-albuterol forced expiratory volume in 1 second
(FEV1)/forced vital capacity (FVC) ratio of =<0.70 and a post-albuterol FEV1 >=30 and
=<80% of predicted normal values calculated using the European Respiratory Society
Global Lung Function Initiative reference equations at Visit 1.

- Smoking history: Current or former cigarette smokers with a history of cigarette
smoking of >= 10 pack-years at Visit 1. Former smokers are defined as those who have
stopped smoking for at least 6 months prior to Visit 1.

Number of pack years = (number of cigarettes per day / 20) x number of years smoked (for
example, 20 cigarettes per day for 10 years, or 10 cigarettes per day for 20 years both
equal 10 pack-years).

Note: Pipe and cigar use cannot be used to calculate pack-year history.

Exclusion Criteria:

- Asthma: A current diagnosis of asthma (Subjects with a prior history of asthma are
eligible if they have a current diagnosis of COPD).

- Other Respiratory Disorders: Known alpha-1 antitrypsin deficiency, active lung
infections (such as tuberculosis), and lung cancer are absolute exclusionary
conditions. Other excluded conditions include and not limited to clinically
significant bronchiectasis, pulmonary hypertension unrelated to COPD, sarcoidosis, or
interstitial lung disease. Or a subject who, in the opinion of the investigator, has
any other significant respiratory conditions in addition to COPD

- Other Diseases/Abnormalities: Subjects with historical or current evidence of
clinically significant cardiovascular, neurological, psychiatric, renal, hepatic,
immunological, endocrine (including uncontrolled diabetes or thyroid disease) or
hematological abnormalities that are uncontrolled and/or a previous history of cancer
in remission for <5 years prior to Visit 1 (localized carcinoma of the skin that has
been resected for cure is not exclusionary). Significant is defined as any disease
that, in the opinion of the investigator, would put the safety of the subject at risk
through participation, or which would affect the efficacy or safety analysis if the
disease/condition exacerbated during the study.

- Poorly controlled COPD: defined as the occurrence of 'acute worsening of COPD that is
managed with corticosteroid and/or antibiotics or that requires treatment prescribed
by a physician in the 6 weeks prior to Screening (Visit 1)', or 'subjects who are
hospitalized due to acute worsening of COPD within 12 weeks of Visit 1'.

- History of COPD exacerbation: subject who have had more than one exacerbation
(moderate or severe) within the 12 months prior to Visit 1.

- Pneumonia and lower respiratory tract infection: Subjects with lower respiratory
tract infection that required the use of antibiotics within 6 weeks prior to Visit 1;
or subjects hospitalized due to pneumonia within 12 weeks of Visit 1.

- Use of long-term oxygen therapy (LTOT): Oxygen therapy prescribed for greater than 12
hours a day. As-needed oxygen use (that is, =<12 hours per day) is not exclusionary.

- Nebulized Therapy: Regular use (prescribed for use every day, not for as-needed use)
of short-acting bronchodilators (for example, albuterol) via nebulized therapy.

- Lung Resection: Lung volume reduction surgery within the 12 months prior to Visit 1.

- Clinically significant abnormal laboratory finding at Visit 1.

- Liver Disease: Current or chronic history of liver disease, or known hepatic or
biliary abnormalities (with the exception of Gilbert's syndrome or asymptomatic
gallstones).

- Presence of hepatitis B surface antigen (HBsAg), or positive hepatitis C antibody
test result at screening. Subjects with positive Hepatitis C antibody due to prior
resolved disease can be enrolled, only if a confirmatory negative Hepatitis C
ribonucleic acid polymerase chain reaction test is obtained.

- Abnormal and clinically significant findings from 12-lead electrocardiogram (ECG)
performed at Visit 1. Site investigators will be provided with ECG over-read
conducted by a centralized independent cardiologist, to assist in evaluation of
subject eligibility. For this study, an abnormal and clinically significant ECG that
would preclude a subject from entering the trial is defined as a 12-lead tracing that
is interpreted as, but not limited to, any of the following:

Sinus bradycardia <45 beats per minute (bpm) (Note: Sinus bradycardia <45 bpm should be
confirmed by two additional readings at least 5 minutes apart) Sinus tachycardia >=110 bpm
(Note: Sinus tachycardia >=110 should be confirmed by two additional readings at least 5
minutes apart) Multifocal atrial tachycardia (wandering atrial pacemaker with rate >100
bpm) PR interval >240 milliseconds (msec) Evidence of Mobitz II second degree or third
degree atrioventricular (AV) block Pathological Q waves (defined as wide [>0.04 seconds]
and deep [>0.4 millivolt (mV) (4 millimeters [mm] with 10 mm/mV setting)] or >25% of the
height of the corresponding R wave, providing the R wave was >0.5 mV [5 mm with 10 mm/mV
setting], appearing in at least two contiguous leads (Note: prior evidence [that is, ECG
obtained at least 12 months prior) of pathological Q waves that are unchanged are not
exclusionary; and the investigator will determine if the subject is precluded from
entering the study) Evidence of ventricular ectopic couplets, bigeminy, trigeminy or
multifocal premature ventricular complexes.

For subjects without complete right bundle branch block: QT interval corrected by
Fridericia's method (QTc[F]) >=450 msec or an ECG that is unsuitable for QT measurements
(for example, poor defined termination of the T wave) For subjects with complete right
bundle branch block: QTc(F) >=480msec or an ECG that is unsuitable for QT measurements
(for example, poor defined termination of the T wave) (Note: All potentially exclusionary
QT measurements should be confirmed by two additional readings at least 5 minutes apart)
ST-T wave abnormalities (excluding non-specific ST-T wave abnormalities) (Note: prior
evidence (that is, ECG obtained at least 12 months prior) of ST-T waves that are unchanged
are not exclusionary and the investigator will determine if the subject is precluded from
entering the study) Clinically significant conduction abnormalities (for example,
Wolff-Parkinson-White syndrome or bifascicular block defined as complete left bundle
branch block or complete right bundle branch block with concomitant left fascicular block)
Clinically significant arrhythmias (for example, atrial fibrillation with rapid
ventricular response, ventricular tachycardia)

- Medication Prior to Spirometry: Unable to withhold albuterol for the 4 hour period
required prior to spirometry testing at each study visit.

- Excluded Medications: Use of the following medications are not permitted within the
defined time intervals prior to Visit 1 and throughout the study:

Depot corticosteroids: 12 weeks Systemic, oral or parenteral corticosteroids: 6 weeks
Antibiotics (for lower respiratory tract infection): 6 weeks 'Cytochrome P450 3A4' strong
inhibitors and 'P-glycoprotein' inhibitor: 4 weeks Long acting beta-agonist (LABA)/inhaled
corticosteroid (ICS) combination products : 4 weeks ICS : 4 weeks Phosphodiesterase 4
(PDE4) inhibitors (roflumilast): 1 week LABA/ Long-acting muscarinic antagonist (LAMA)
combination (for example, vilanterol/umeclidinium bromide): 1 week Once-daily
beta2-agonist (for example, Olodaterol and Indacaterol): 1 week LAMA (tiotropium,
aclidinium, glycopyrronium, umeclidinium): 1 week Theophylline preparations: 48 hours Oral
leukotriene inhibitors (zafirlukast, montelukast, zileuton): 48 hours Oral beta2-agonists
Long-acting: 48 hours Short-acting: 12 hours Inhaled LABA (for example, Salmeterol,
formoterol): 48 hours Inhaled sodium cromoglycate or nedocromil sodium: 24 hours Inhaled
short acting beta2-agonists: 4 hours Inhaled short-acting anticholinergics: 4 hours
Inhaled short-acting anticholinergic/short-acting beta2-agonist combination products: 4
hours Use of study provided albuterol is permitted during the study, except in the 4-hour
period prior to spirometry testing

- Drug or Alcohol Abuse: A known or suspected history of alcohol or drug abuse within 2
years prior to Visit 1.

- Contraindications: Any history of allergy or hypersensitivity to any
anticholinergic/muscarinic receptor antagonist, beta-2-agonist, sympathomimetic,
corticosteroid (intranasal, inhaled or systemic) lactose/milk protein, or a medical
condition such as narrow-angle glaucoma, prostatic hypertrophy or bladder neck
obstruction, that, in the opinion of the study physician contraindicates study
participation or use of an inhaled LAMA, LABA or ICS

- 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)

- Affiliation with Investigator Site: A subject will not be eligible for this study if
he/she is an immediate family member of the participating investigator,
sub-investigator, study coordinator, or employee of the participating investigator.

- Inability to read: In the opinion of the investigator, any subject who is unable to
read and/or would not be able to complete a diary.

- Questionable validity of consent: Subjects with a history of psychiatric disease,
intellectual deficiency, poor motivation or other conditions that will limit the
validity of informed consent to participate in the study.

- Non-compliance: Subjects at risk of non-compliance, or unable to comply with the
study procedures. Any infirmity, disability, or geographic location that would limit
compliance for scheduled visits.