HomeTrialNCT07016412
NCT07016412Phase 2RECRUITING

A Phase IIb Ensifentrine-glycopyrrolate Fixed-dose Combination Dose Ranging Study in Subjects With COPD

Study Summary

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).

View on ClinicalTrials.gov ↗
Study Details
Enrollment480 participants
Primary Completion
Lead SponsorVerona Pharma plc
Data Retrieved2026-04-11 04:31:16.186906+00:00
What This Trial Means for Biotech Investors
Trial Phase Context

Phase 2 trials begin testing efficacy in a larger patient group (100–300). This is often where biotech binary events occur — positive Phase 2 data can significantly advance a company's pipeline narrative, while failures can be terminal for a program.

Status & Expected Data

Currently recruiting: the trial is enrolling patients. A data readout is not expected until after enrollment closes and the follow-up period is complete.

Enrolled: 480 participants
Sponsor Catalyst Profile

Verona Pharma (VRNA) is the sponsoring company for this trial. BiotechSign currently grades this company D (45/100) based on composite catalyst signals across its full pipeline. This trial is one data point in that overall catalyst picture.

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