Budesonide/glycopyrrolate/formoterol fumarate (Breztri Aerosphere) 320 μg/18 μg/9.6 μg administered as two inhalations, twice daily.
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Phase 35
ApprovedAbout Budesonide/glycopyrrolate/formoterol fumarate (Breztri Aerosphere) 320 μg/18 μg/9.6 μg administered as two inhalations, twice daily.
Budesonide/glycopyrrolate/formoterol fumarate (Breztri Aerosphere) 320 μg/18 μg/9.6 μg administered as two inhalations, twice daily. is a approved stage product being developed by AstraZeneca for COPD. The current trial status is withdrawn. This product is registered under clinical trial identifier NCT05970263. Target conditions include COPD.
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Clinical Trials (1)
| NCT ID | Phase | Status |
|---|---|---|
| NCT05970263 | Approved | Withdrawn |
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