Viewing Study NCT04564456


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Ignite Modification Date: 2026-05-30 @ 5:45 AM
Study NCT ID: NCT04564456
Status: COMPLETED
Last Update Posted: 2021-01-20
First Post: 2020-09-22
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: A Pivotal Bioequivalence Study Between Fluticasone Propionate 500 mcg and Salmeterol Xinafoate 50 mcg Inhalation Powder/Respirent Pharmaceuticals vs. ADVAIR DISKUSĀ® 500/50 Inhalation Powder/GSK in Healthy Volunteers
Sponsor: Respirent Pharmaceuticals Co Ltd.
Organization:

Organization Data

Organization:
Class: INDUSTRY
Study ID: BREATH-BE500-PIVOTAL
Study Type: None
Study Domain: None
Study Link: None
Lead Sponsor:
Lead Sponsor Class: INDUSTRY
Responsible Party:
Responsible Party Title:
Responsible Party Type: SPONSOR
Responsible Party Affiliation:
Old Name: None
Old Organization: None

Collaborators

Collaborators

Name Class View
None INDUSTRY View