Therapeutic Equivalence of Fluticasone Propionate Pressurized Metered Dose Inhaler, 110 mcg, to Flovent® HFA 110 mcg

Inclusion Criteria:

1. Adult ≥18 and ≤75 years of age male or female subjects of non-child bearing potential
or of child bearing potential committing to consistent and correct use of an
acceptable method of birth control.

2. Body mass index (BMI) ≥18 and ≤45.

3. Diagnosis of asthma, as defined by the NAEPP-EPR3 at least 12 months prior to
Enrollment at Screening Visit 1a.

4. Pre bronchodilator highest forced expiratory volume in 1 second (FEV1) ≥45% and ≤85%
of predicted normal value at Screening Visit 1b and on the first day of treatment
prior to randomization.

5. Reversibility of airway obstruction ≥15% of FEV1 within 30 minutes of 360mcg albuterol
inhalation (4 puffs).

6. Subjects should be stable on their chronic asthma treatment regimen for at least 4
weeks prior to Enrollment at Screening Visit 1a.

7. Currently non-smoking, defined as abstinence from all smoking, including marijuana and
all tobacco products (i.e., e-cigarettes, cigarettes, cigars, pipe, ortobacco) within
the past year, a negative cotinine screening test at Screening Visit 1b, and <10 pack
years of historical use.

8. Able to replace current short-acting β agonist (SABA) with study issued albuterol
inhaler for use as needed for the duration of the study.

9. Able to withhold all inhaled SABAs for at least 6 hours prior to lung function
assessments on study visits.

10. Able to withhold all inhaled long acting β agonists (LABA) 24 hours before Screening
Visit 1b.

11. Able to discontinue current asthma medications (e.g., inhaled corticosteroids[ICS],
LABA, etc.) during the Run-in period and for remainder of the study.

12. Able to comply with study procedures, including correct use of inhaler devices and
home peak expiratory flow (PEF) device, and maintaining an electronic diary (eDiary).

13. Willingness to give their written informed consent to participate in the study.

Exclusion Criteria:

1. Life-threatening asthma, defined as a history of asthma episodes(s) requiring
intubation, and/or associated with hypercapnia, respiratory arrest or hypoxic
seizures, asthma related syncopal episode(s), or hospitalizations due to asthma within
the past year prior to Enrollment, or during the Screening or Run-in period.

2. History of significant respiratory disease other than asthma (e.g., chronic
obstructive pulmonary disease [COPD], interstitial lung disease, chronic bronchitis,
emphysema, etc.).

3. Evidence or history of clinically significant disease or abnormality including
congestive heart failure, uncontrolled hypertension, uncontrolled coronary artery
disease, myocardial infarction, or cardiac dysrhythmia. In addition, historical or
current evidence of significant hematologic, hepatic, neurologic, psychiatric, renal,
cardiovascular, endocrine, or other diseases that, in the opinion of the Investigator,
would put the subject at risk through study participation, or would affect the study
analyses if the disease exacerbates during the study.

4. Viral or bacterial, upper/lower respiratory tract infection (U/LRTI), or sinus, or
middle ear infection within 4 weeks prior to Screening Visit 1b, during the Run-in
period, or on the first day of treatment prior to randomization.

5. Hypersensitivity to any sympathomimetic drug (e.g., albuterol) or any inhaled,
intranasal, or systemic corticosteroid therapy.

6. Hypersensitivity to any of the ingredients of FP pMDI or Flovent HFA.

7. Subjects receiving β2 blockers, anti-arrhythmics, anti-depressants, and/or monoamine
oxidase inhibitors within 4 weeks prior to Screening Visit 1b.

8. Subjects who required systemic or oral corticosteroids (for any reason) within the
past 6 months prior to Screening Visit 1b.

9. Subjects receiving medications that are strong cytochrome P4503A4 inhibitors (e.g.,
ritonavir, ketoconazole, itraconazole) within 2 weeks prior to Screening Visit 1b.

10. Subjects receiving any approved or investigational biological treatment for asthma
(e.g., omalizumab, mepolizumab) within 6 months prior to Screening Visit 1b.

11. Subjects with clinically relevant abnormal chemistry laboratory findings at Screening
Visit 1b as assessed by the Investigator.

12. Subjects with clinically significant electrocardiogram (ECG) findings at Screening
Visit 1b as assessed by the Investigator and/or cardiologist.

13. Subjects who have received any Investigational Product (IP) within 1 month prior to
Screening Visit 1b and as described in the Washout Table in Appendix 1.

14. Female subjects who are pregnant or breast feeding.

15. Evidence of oral candidiasis at Screening or randomization, or history within 1year
prior to Screening Visit 1b.

16. Evidence or history of tuberculosis, hypercorticism, or adrenal suppression.

17. Evidence or history within the 6 months prior to Screening Visit 1b of clinically
relevant eye problems such as cataracts. Any previous diagnosis or treatment for
ocular hypertension or glaucoma is exclusionary.

18. Subjects with hyperbilirubinemia (defined as aspartate aminotransferase [AST] or
alanine aminotransferase [ALT] ≥3 times the upper limit of the normal range [ULN], or
bilirubin ≥2 times the ULN) or Hy's Law events.

19. Evidence or history of drug or alcohol abuse in the 2 years prior to Enrollment at
Screening Visit 1a or a positive drug or alcohol test at Screening Visit 1b.