A 12-week Study to Assess the Efficacy and Safety of Budesonide and Formoterol Fumarate Metered Dose Inhaler Relative to Budesonide Metered Dose Inhaler in Participants With Inadequately Controlled Asthma (LITHOS)

Last updated:
2026-07-18
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View trial details

Overview

Official protocol title:

A RANDOMIZED, DOUBLE-BLIND, PARALLEL GROUP, MULTICENTER 12 WEEK STUDY TOASSESS THE EFFICACY AND SAFETY OF BUDESONIDE AND FORMOTEROL FUMARATE METERED DOSE INHALER RELATIVE TO BUDESONIDE METERED DOSE INHALER IN PARTICIPANTS WITH INADEQUATELY CONTROLLED ASTHMA (LITHOS)

Intervention/treatment:
BUDESONIDE-FORMOTEROL/ BUDESONIDE
Medical condition:
ASTHMA
Protocol code:
D5982C00005
Control number:
269480
Status:
Closed
Approved:
December 05, 2022
Date Completed:
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT05755906
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
12 Years to 80 Years
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Global Clinical Lead
Organization
AstraZeneca
Phone:
1-877-240-9479
Sponsor
ASTRAZENECA CANADA INC

Locations

British Columbia

Research Site
Kamloops, British Columbia, V2C 5T1
Research Site
Kelowna, British Columbia, V1Y 4N7
Research Site
Penticton, British Columbia, V2A 5L5

Ontario

Research Site
Ajax, Ontario, L1S 2J5
Research Site
Toronto, Ontario, M9V 4B4
Research Site
Winchester, Ontario, K0C 2K0
Research Site
Windsor, Ontario, N8X 2G1

Quebec

Research Site
Montreal, Quebec, H3M 1L3
Research Site
Québec, Quebec, G1G 3Y8
Research Site
Québec, Quebec, G1V 4W2

Results

See the results from the trial NCT05755906. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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