Study on the Safety and Efficacy of PA9159 Inhalation Aerosol for the Treatment of Adult Bronchial Asthma

NCT07324707 | Recruiting Phase 2

• 1 other identifier: PA9159AS-202
• Study Type: interventional
• Target: 30
• Locations: 1 country
• Sites: 1

Brief Summary

PA9159 is a highly potent novel corticosteroid. The purpose of this study is to evaluate the safety, efficacy and characteristics of population pharmacokinetics of multiple dosing of PA9159 Inhaler in patients with bronchial asthma.

Conditions

Bronchial Asthma

Outcome Measures

Primary Outcomes (1)

• Evaluation the change in morning pre-dose forced expiratory volume in one second (FEV1) from baseline to week 4 of treatment.

  After the subject takes a deep breath as much as possible, the volume of air that can be exhaled in the first second when exhaling with maximum force and speed. This is one of the most core indicators in pulmonary function tests, directly reflecting the patency of the airways (especially the large airways). A lower FEV₁ value indicates more severe airway obstruction. Therefore, the difference is calculated as the value after 28 days of treatment minus the baseline value. A larger upward change indicates more significant symptom improvement.

  From pre-dose until 28 days post-dose

Secondary Outcomes (7)

• Evaluation the change from baseline in pre-dose FEV1 at week 1 and week 2 of treatment.

  From pre-dose until 14 days post-dose

• Evaluation the change from baseline in pre-dose morning and evening peak expiratory flow (PEF) at weeks 1, 2, and 4 of treatment.

  From pre-dose until 28 days post-dose

• Proportion of patients with asthma exacerbations during the treatment period.

  From pre-dose until 28 days post-dose

• Proportion and frequency of patients using rescue medication over the 4-week treatment period.

  From pre-dose until 28 days post-dose

• Evaluation the change from baseline in the Asthma Control Test (ACT) score after 4 weeks of treatment.

  From pre-dose until 28 days post-dose

Study Arms (2)

PA9159 120 μg

EXPERIMENTAL

Fifteen subjects will be randomly assigned to receive 120 μg of PA9159 Metered-Dose Inhaler for 28 days. Subjects will be administered one vial of drug Twice a day: In the morning, take 2 puffs . In the evening, take 2 puffs .

Drug: PA9159 Metered-Dose Inhaler, 120 μg per day for 28 days

Fluticasone Propionate Inhaled Aerosol 200 μg

ACTIVE COMPARATOR

Fifteen subjects will be randomly assigned to receive 200 μg of Fluticasone Propionate Inhaled Aerosol for 28 days. Subjects will be administered one vial of drug Twice a day: In the morning, take 2 puffs . In the evening, take 2 puffs .

Drug: Fluticasone Propionate Inhaled Aerosol 200 μg per day for 28 days

Interventions

PA9159 Metered-Dose Inhaler, 120 μg per day for 28 days DRUG

PA9159 of 120 μg is delivered orally through a metered-dose Inhaler , Twice daily for 28 days.

PA9159 120 μg

Fluticasone Propionate Inhaled Aerosol 200 μg per day for 28 days DRUG

Fluticasone Propionate Inhaled Aerosol of 200 μg is delivered orally through a metered-dose Inhaler , Twice daily for 28 days.

Fluticasone Propionate Inhaled Aerosol 200 μg

Eligibility Criteria

• Age: 18 Years - 75 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Aged 18 to 75 years inclusive, regardless of gender;
• According to the definition in the Chinese "Guidelines for Prevention and Treatment of Bronchial Asthma (2020 Edition)," subjects diagnosed with bronchial asthma, including those with an initial diagnosis of asthma, or those diagnosed with asthma during childhood or adolescence with stable condition who have not received long-term treatment but exhibit significantly more pronounced symptoms in adulthood and/or recently compared to the past;
• Pre-randomization, pulmonary function tests show 60% ≤ FEV1% predicted ≤ 85%;
• Any objective test result indicating variable airflow limitation conducted within 1 year prior to screening is positive, or the bronchodilator test during the screening period is positive, i.e., an increase in FEV1 ≥ 12% and an absolute increase in FEV1 ≥ 200 mL 15-30 minutes after inhaling 400 μg salbutamol (if the bronchodilator test result does not meet the positive threshold, a repeat bronchodilator test is allowed within 14 days after the test \[excluding the test day\]); or the bronchial provocation test is positive, i.e., a decrease in FEV1 ≥ 20% after inhaling a provocant (methacholine or histamine); or the average daily diurnal variability of peak expiratory flow (PEF) (calculated as the sum of daily PEF diurnal variability over 7 consecutive days divided by 7) \> 10%;
• Voluntarily sign the informed consent form.

You may not qualify if:

• Subjects who are unable to correctly use a nebulizer, cannot tolerate nebulized inhalation administration, or fail inhalation administration training;
• Subjects with other pulmonary diseases, including chronic obstructive pulmonary disease, bronchiectasis, pulmonary fibrosis, tuberculosis, etc., for which, in the investigator's judgment, asthma remains the dominant condition;
• Coexistence of other clinically significant conditions that may affect lung function, including but not limited to pleural diseases, mediastinal diseases, diaphragmatic disorders, myasthenia, thoracic deformities, etc.;
• History of severe cardiovascular diseases, such as congestive heart failure, coronary artery disease, myocardial infarction, arrhythmia, uncontrolled hypertension (resting seated systolic blood pressure ≥ 160 mmHg or diastolic blood pressure ≥ 100 mmHg on two or more consecutive measurements), etc., which, in the investigator's judgment, would put the subject at risk or may affect the interpretation of study results;
• Subjects with hyperthyroidism, assessed by the investigator as unsuitable for participation in this trial;
• History of severe hematologic, hepatic, psychiatric, renal, or other diseases that, in the investigator's judgment, would put the subject at risk or may affect the interpretation of study results;
• History of malignancy within the past five years (excluding cured cervical intraepithelial neoplasia, thyroid cancer, or basal cell carcinoma of the skin diagnosed and cured within 5 years);
• Subjects who have undergone or are expected to undergo solid organ or bone marrow transplantation within the next year;
• Hypokalemia (serum potassium \< 3.5 mmol/L during screening);
• Type I diabetes or poorly controlled Type II diabetes (fasting blood glucose \> 11.1 mmol/L during screening);
• Known or pre-randomization examination revealing oral, pharyngeal, or esophageal candidiasis;
• Abnormal liver or kidney function during screening (ALT and/or AST \> 2× upper limit of normal; Scr \> 1.5× upper limit of normal);
• Positive hepatitis B surface antigen or hepatitis B core antibody with HBV DNA ≥ 2000 IU/mL, positive hepatitis C antibody with HCV RNA ≥ 1000 IU/mL, positive human immunodeficiency virus antibody, or history of acquired immunodeficiency syndrome;
• Known allergy to any component of inhaled corticosteroids or salbutamol preparations;
• Respiratory tract infection, sinus infection, or acute otitis media within 4 weeks before screening or during the run-in period, which, in the investigator's judgment, would lead to changes in asthma treatment or affect the subject's asthma status;

Sponsors & Collaborators

• Anhui Palo Alto Pharmaceuticals, Inc.: lead

Study Sites (1)

The First Affiliated Hospital of Nanchang University

Nanchang, Jiangxi, 330006, China

RECRUITING

MeSH Terms

Conditions

Asthma

Condition Hierarchy (Ancestors)

Bronchial Diseases; Respiratory Tract Diseases; Lung Diseases, Obstructive; Lung Diseases; Respiratory Hypersensitivity; Hypersensitivity, Immediate; Hypersensitivity; Immune System Diseases

Study Officials

• Wei Zuo

  The First Affiliated Hospital of Nanchang University

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Mengli Kan

CONTACT

86-15618775927; kanmengli@paloaltopharma.com

Chunping Lu

CONTACT

86-15921612878; luchunping@paloaltopharma.com

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: December 24, 2025
• First Posted: January 7, 2026
• Study Start: October 15, 2025
• Primary Completion: March 1, 2026
• Study Completion: March 1, 2026
• Last Updated: January 7, 2026

Record last verified: 2025-12

Data Sharing

• IPD Sharing: Will not share

Locations

CN (1)