A Study Comparing Efficacy, Safety and Tolerability of the Fixed Dose Triple Combination CHF 5993 With the Fixed Dose Dual Combination CHF 1535 in Subjects With COPD

Last updated:
2026-07-18
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View trial details

Overview

Official protocol 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 ADMINISTERED VIA PMDI IN SUBJECTS WITH CHRONIC OBSTRUCTIVE PULMONARY DISEASE (COPD)

Intervention/treatment:
BECLOMETHASONE-FORMOTEROL-GLYCOPYRRONIUM (CHF 5993) / BECLOMETHASONE-FORMOTEROL (CHF 1535)
Medical condition:
CHRONIC OBSTRUCTIVE PULMONARY DISEASE (COPD)
Protocol code:
CLI-05993AA3-06
Control number:
272354
Status:
Closed
Approved:
March 17, 2023
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT04320342
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
40 Years and older
Accepts healthy volunteers: No

Contacts and locations

Contact
Sponsor
CHIESI FARMACEUTICI S.P.A.

Locations

Alberta

Chiesi Clinical Trial Site 124103
Edmonton, Alberta, T5A 4L8
Chiesi Clinical Trial Site 124105
Sherwood Park, Alberta, T8H 0N2

Ontario

Chiesi Clinical Trial Site 124100
Windsor, Ontario, N8X 1T3
Chiesi Clinical Trial Site 124102
Burlington, Ontario, L7N 3V2
Chiesi Clinical Trial Site 124104
Greater Sudbury, Ontario, P3C 1X3

Quebec

Chiesi Clinical Trial Site 124106
Trois-Rivières, Quebec, G8T 7A1
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