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Clinical Trial Summary

- To provide a therapeutic option for patients not able to take the oral formulation of TPOXX (e.g., cannot swallow, vomiting) and who have confirmed or suspected (based on clinical signs and symptoms with known exposure while laboratory confirmation may be pending) orthopox virus infections OR who have a significant vaccinia adverse reaction (as defined in the protocol) resulting from vaccinia vaccination, secondary transmission, or other exposure; - To collect data on the safety of TPOXX IV (tecovirimat injection, 10 mg/mL).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05380752
Study type Expanded Access
Source U.S. Army Medical Research and Development Command
Contact Force Health Protection
Phone 301-401-2768
Email usarmy.detrick.medcom-usammda.mbx.force-health-protection@mail.mil
Status Available
Phase