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NCT06742736 · ClinicalTrials.gov registry record

EXACERBATIONS AND REAL-WORLD OUTOMES INCLUDING CARDIOPULMONARY EVENTS AMONG PATIENTS WITH CHRONIC OBSTRUCTIVE PULMONARY DISEASE (MITOS: EROS+CP US Study)

A clinical trial, sponsored by AstraZeneca.

Completed
Registry status
13,000
Enrollment target

NCT06742736: Completed study, sponsored by AstraZeneca.

NCT06742736 is a clinical trial that has completed, run by AstraZeneca. The registered enrollment target is 13,000 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06742736 has completed, sponsored by AstraZeneca.

COMPLETED
Registry status
13,000 participants
Enrollment target

Study Summary

A retrospective real-world data study, assessing the relationship between the timing of Budesonide/Glycopyrrolate/Formoterol initiation following an exacerbation and the occurrence of subsequent exacerbations, severe cardiopulmonary events and other real-world outcomes in the United States

Primary Outcome

Annualized rates of COPD exacerbation events observed from index date (qualifying exacerbation event) through study completion (or until end of data availability; mean follow-up 462 days

Interventions

  • DRUG BGF

Trial Details

FieldValue
Enrollment Target 13,000 participants
Start Date 2024-05-31
Est. Completion 2024-09-30
AstraZeneca

1,285 total trials

What the finished NCT06742736 record still lists

NCT06742736 is an observational study that tracks outcomes without assigning an intervention. Its 13,000 participants enrollment target places it among the larger protocols in the corpus.

The record links to 0 conditions, and to 1 intervention - of which BGF is the first listed.

NCT06742736 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06742736 about?

NCT06742736 is a clinical study titled "EXACERBATIONS AND REAL-WORLD OUTOMES INCLUDING CARDIOPULMONARY EVENTS AMONG PATIENTS WITH CHRONIC OBSTRUCTIVE PULMONARY DISEASE (MITOS: EROS+CP US Study)". A retrospective real-world data study, assessing the relationship between the timing of Budesonide/Glycopyrrolate/Formoterol initiation following an exacerbation and the occurrence of subsequent exacerbations, severe cardiopulmonary events and other real-world outcomes in the United States

What is the current status of trial NCT06742736?

This trial is currently completed. The enrollment target is 13,000 participants. The study started on 2024-05-31. Estimated completion is 2024-09-30.

What interventions are being tested in trial NCT06742736?

The interventions under investigation include: BGF (DRUG).

Who is sponsoring clinical trial NCT06742736?

This trial is sponsored by AstraZeneca, which has 1,285 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT06742736, the US trial registry maintained by the National Library of Medicine. NCT06742736 (large enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.