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A Multi-centre, Prospective, Observational Post-Authorization Safety Study to Evaluate the Safety Profile of Budesonide/Glycopyrrolate/Formoterol MDI in Chinese Patients With COPD in Routine Clinical Practice

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A Multi-centre, Prospective, Observational Post-Authorization Safety Study to Evaluate the Safety Profile of Budesonide/Glycopyrrolate/Formoterol MDI in Chinese Patients With COPD in Routine Clinical Practice

Status: Completed
Phase of Trial: Phase IV

Latest Information Update: 01 Aug 2024

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At a glance

  • Drugs Budesonide/formoterol/glycopyrrolate (Primary)
  • Indications Chronic obstructive pulmonary disease
  • Focus Adverse reactions
  • Acronyms TORES
  • Sponsors AstraZeneca

    • Most Recent Events

    • 05 Dec 2023 Status changed from recruiting to completed.
    • 07 Aug 2023 Planned End Date changed from 30 Jan 2024 to 31 Oct 2023.
    • 07 Aug 2023 Planned primary completion date changed from 30 Jan 2024 to 31 Oct 2023.

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