umeclidinium 62.5 µg and vilanterol 25 µg + Revefenacin 175 µg, Formoterol 20 µg + Placebo ( Revefenacin and Formoterol ) + Placebo DPI

ApprovedRecruiting
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80
Hype Score

Development Stage

Pre-clinical
Phase 1
Phase 2
Phase 3
5
Approved
Indication / Disease

COPD (Chronic Obstructive Pulmonary Disease)

Conditions

COPD (Chronic Obstructive Pulmonary Disease)

Trial Timeline

Dec 5, 2023 → Dec 1, 2025

About umeclidinium 62.5 µg and vilanterol 25 µg + Revefenacin 175 µg, Formoterol 20 µg + Placebo ( Revefenacin and Formoterol ) + Placebo DPI

umeclidinium 62.5 µg and vilanterol 25 µg + Revefenacin 175 µg, Formoterol 20 µg + Placebo ( Revefenacin and Formoterol ) + Placebo DPI is a approved stage product being developed by Theravance Biopharma for COPD (Chronic Obstructive Pulmonary Disease). The current trial status is recruiting. This product is registered under clinical trial identifier NCT07133880. Target conditions include COPD (Chronic Obstructive Pulmonary Disease).

Hype Score Breakdown

Clinical
30
Activity
20
Company
5
Novelty
10
Community
12

Clinical Trials (1)

NCT IDPhaseStatus
NCT07133880ApprovedRecruiting

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