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TRITON Study for Adults with COPD
Protocol: STUDY00006846
Full Title
A phase III, 52-week, multinational, multicenter, randomized, double-blind, 2-arm parallel group study comparing efficacy, safety and tolerability of the fixed dose triple combination of beclomethasone dipropionate plus formoterol fumarate plus glycopyrronium bromide (CHF 5993) with the fixed dose dual combination of beclomethasone dipropionate plus formoterol fumarate (CHF 1535), both administere
Description
The University at Buffalo (UB) Department of Medicine is looking for adults with chronic obstructive pulmonary disease (COPD) for a clinical trial. The goal of the study is to compare new combinations of bronchodilators (medications that open up the airways) and inhaled corticosteroids (anti-inflammatory medication) in people with COPD to better control their symptoms and prevent exacerbations (flare-ups).

Participants will be enrolled in the study for about 55 weeks and complete 12 in-person study visits. They will complete physical exams, lab tests, and surveys. Participants will administer the study drugs daily via inhalers. They can earn up to $728 for completing all study visits.
Compensation: Yes
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Compensation may include cash, checks, gift cards, debit cards, or incentives like gift baskets, technology items, or merchandise.
Eligibility
Adults 40 years or older Have been diagnosed with chronic obstructive pulmonary disease (COPD) at least 12 months before participating
Age Group: Adults
Principal Investigator: SANJAY SETHI
ClinicalTrials.gov: Open Study
Contact(s)
CATHERINE WRONA
wrona@buffalo.edu
+1 716-888-4713

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