A 24-week Prospective, Open-label, Multicenter, Single-arm Regulatory Post-Marketing Surveillance (rPMS) Study in Real-world Setting (Mandatory by Local HA Regulation) for Atectura® (QMF149 150/80 μg o.d., QMF149 150/160 μg o.d. and QMF149 150/320 μg o.d. Via Breezhaler)
Latest Information Update: 17 Jan 2025
At a glance
- Drugs Indacaterol/mometasone (Primary)
- Indications Asthma
- Focus Adverse reactions
- Sponsors Novartis Pharmaceuticals
Most Recent Events
- 30 Aug 2022 Status changed from not yet recruiting to recruiting.
- 31 May 2022 Planned initiation date changed from 2 May 2022 to 30 Jun 2022.
- 29 Apr 2022 Planned number of patients changed from 660 to 600.