4
Participants
Start Date
December 29, 2021
Primary Completion Date
June 28, 2022
Study Completion Date
July 8, 2022
Famotidine
80 mg tablet, QID for 14 days
Celecoxib
400 mg (initial dose), then 200 mg capsule, BID for 5 days
Placebo
tablet, QID for 14 days; capsule, BID for 5 days
Integrated Therapeutic Solutions USA, Inc., New York
Integrated Therapeutic Solutions USA, Inc., Huntingdon
Integrated Therapeutic Solutions USA, Inc, Rockville
Integrated Therapeutic Solutions USA, Inc, Gaithersburg
Integrated Therapeutic Solutions USA, Inc, Frederick
Integrated Therapeutic Solutions USA, Inc., Charleston
Integrated Health Solutions USA, Inc., Atlanta
Integrated Therapeutic Solutions USA, Inc, Hazlehurst
Integrated Therapeutic Solutions USA, Inc., Miami
Integrated Therapeutic Solutions USA, Inc, Prospect
Integrated Therapeutic Solutions USA, Inc, Dearborn
Integrated Therapeutic Solutions USA, Inc., Chicago
Integrated Therapeutic Solutions USA, Inc., Dallas
Integrated Therapeutic Solutions USA, Inc., Newport Beach
Integrated Therapeutic Solutions USA, Inc., Newark
Lead Sponsor
United States Department of Defense
FED
Leidos Life Sciences
INDUSTRY