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Study identifier: NCT07016412 Synced from ClinicalTrials.gov · August 03, 2026
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A Phase IIb Ensifentrine-glycopyrrolate Fixed-dose Combination Dose Ranging Study in Subjects With COPD

Condition: Chronic Obstructive Pulmonary Disease  ·  Sponsor: Verona Pharma, Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA

PhasePhase 2
Planned participants1119
Who can joinAll sexes, 40 Years to 80 Years
Healthy volunteersNo

About this study

This study will assess the safety and efficacy of fixed dose combinations of ensifentrine with two different glycopyrrolate dose levels compared to placebo and to the individual components of the fixed dose combinations, each administered twice a day via standard jet nebulizer, in adult subjects with chronic obstructive pulmonary disease (COPD).

This description comes directly from the study's public registry record.

Talk to the study team

No contact information is available for this study as per the public registry record.

Always discuss trial participation with your own doctor first.

Locations (57)

SEC Clinical Research, LLCDothan, Alabama, United States
Elite Clinical Studies, LLCPhoenix, Arizona, United States
Tucson Clinical Research InstituteTucson, Arizona, United States
Downtown LA Research Center Inc - ClinEdgeLos Angeles, California, United States
California Medical Research Associates, Inc.Northridge, California, United States
Northern California Research CorpSacramento, California, United States
Clinical Research of West Florida IncClearwater, Florida, United States
Fleming Island Center For Clinical ResearchFleming Island, Florida, United States
Florida Institute For Clinical Research LLCOrlando, Florida, United States
Ormond Beach Clinical ResearchOrmond Beach, Florida, United States
Progressive Medical ResearchPort Orange, Florida, United States
Clinical Research of West Florida Inc - TampaTampa, Florida, United States

+ 45 more locations — full list on the registry record.

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