A 24-week Prospective, Open-label, Multicenter, Single-arm rPMS Study in Real-world Setting for Atectura®

Recruiting

• Conditions: Asthma
• Interventions: Other: Atectura inhalation capsule (150/80ug); Other: Atectura inhalation capsule (150/160ug); Other: Atectura inhalation capsule (150/320ug)

• Registration Number: NCT05217810
• Lead Sponsor: Novartis Pharmaceuticals

Brief Summary

This surveillance was designed as a prospective, open-label, multicenter, single-arm, non-interventional, observational study to evaluate the safety and effectiveness of Atectura inhalation capsule for up to 24 weeks under routine clinical practice.

Detailed Description

The three different doses of Atectura inhalation capsule via Breezhaler will be prescribed according to the approved label information in Korea, and the investigation for any additional diagnostic or monitoring will be not conducted for this study

Basic Information
|
Recruitment & Eligibility
|
Study & Design
|
Trial Locations

Study Timeline

• Study First Submitted: 2021-11-30
• Study First Submitted QC: 2022-01-19
• Study First Posted: 2022-02-01
• Study Start: 2022-05-09
• Status Verified: 2024-02
• Last Update Submitted: 2024-02-07
• Last Update Posted: 2024-02-08
• Primary Completion: 2026-12-23
• Study Completion: 2026-12-23

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 600

Inclusion Criteria

1. Adolescent (≥12 years of age) and adult patients with a physician's diagnosis of asthma, who are prescribed Atectura inhalation capsule (indacaterol acetate/mometasone furoate; 150/80, 150/160, 150/320 μg) via Breezhaler, as per the approved label information
2. Patients who participate in the study after signing the consent form for data collection and use (Data Privacy ICF) after receiving a clear explanation of the objectives and nature of the study from the investigator (For patients under the age of 18, consent and signature of a legal representative is required)

Read More

Exclusion Criteria

1. Patients who are contraindicated for this medicinal product as described in the Precautions for Use in the label information (package insert) A. Patients with hypersensitivity reaction to this medicinal product or any of its constituents B. Because this medicinal product contains lactose, patients with hereditary problems of galactose intolerance, the Lapp lactose deficiency or glucose-galactose malabsorption, etc.
2. Patients with acute asthma symptoms, including acute episodes of bronchospasm, for which a short-acting bronchodilator is required
3. Patients participating in other interventional clinical trials

Read More

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Atectura inhalation capsule (150/80ug)	Atectura inhalation capsule (150/80ug)	Indacaterol acetate/Mometasone furoate; 150/80ug
Atectura inhalation capsule (150/160ug)	Atectura inhalation capsule (150/160ug)	Indacaterol acetate/Mometasone furoate; 150/160ug
Atectura inhalation capsule (150/320ug)	Atectura inhalation capsule (150/320ug)	Indacaterol acetate/Mometasone furoate; 150/320ug

Primary Outcome Measures

Name	Time	Method
Incidence of unexpected adverse events and unexpected serious adverse events	24 weeks	Incidence of unexpected AE and SAE will be collected. The term "unexpected" means not listed in local label
Incidence of adverse events and serious adverse events	24 weeks	Incidence of AE and SAE will be collected

Secondary Outcome Measures

Name	Time	Method
Baseline characteristics of patients in relation to the investigator assessment	12 weeks	Logistic regression analysis will be performed to determine factors affecting the effectiveness (improved) in the investigator assessment, out of baseline characteristics (age (\<65 vs. ≥65 years), male vs. female, pregnancy (yes vs. no), family history (yes vs. no), exacerbation history (0 vs. above 1), smoking history (yes vs. no), comorbidity (yes vs. no), concomitant medication/ therapy (yes vs. no)), study treatment information, and special populations.
change from baseline in trough FEV1	Baseline, week 12	Forced Expiratory Volume in one second (FEV1) is calculated as the volume of air forcibly exhaled in one second as measured by a spirometer.
Effective rate and ineffective rate by investigator assessment	week 12	Effective (improved) rate and ineffective (unchanged/aggravated) rate by investigator assessment
change from baseline in ACT score	Baseline, week 12	The Asthma Control Test (ACT) is a validated tool to assess overall asthma control. It is a 1 page questionnaire consisting of 5 simple questions assessing: asthma symptoms, use of rescue medications, and the impact of asthma on everyday functioning. All questions are scored on a 5-point Likert scale, with a higher score indicating better control. All scores are added together to calculate a total score. Total score ranges from 5 to 25. A positive change indicates improvement.
Baseline characteristics of patients showing adverse events/adverse drug reactions	24 weeks	The incidence rates of AEs/ADRs will be presented by factors, such as subject baseline characteristics (age (\<65 vs. ≥65 years), male vs. female, pregnancy (yes vs. no), family history (yes vs. no), exacerbation history (0 vs. above 1), smoking history (yes vs. no), comorbidity (yes vs. no), concomitant medication/ therapy (yes vs. no)), study treatment information, and special populations.
Baseline characteristics of patient in relation to changes from baseline through FEV1 and ACT score	12 weeks	Regression analysis will be performed to determine factors affecting the change in trough FEV1 and ACT score, out of baseline characteristics (age (\<65 vs. ≥65 years), male vs. female, pregnancy (yes vs. no), family history (yes vs. no), exacerbation history (0 vs. 1), smoking history (yes vs. no), comorbidity (yes vs. no), concomitant medication/ therapy (yes vs. no)), study treatment information, and special populations

Trial Locations

Locations (1)

Novartis Investigative Site; 🇰🇷 Daegu, Dalseo Gu, Korea, Republic of