Tecovirimat (ST-246) Treatment for Orthopox Virus Exposure

NCT02080767 · Status: AVAILABLE · Type: EXPANDED_ACCESS

Last updated 2025-03-06

No results posted yet for this study

Summary

The purpose of this clinical protocol is to treat individuals with Tecovirimat after exposure to orthopox viruses.

Conditions

Interventions

DRUG

Tecovirimat

Oral tablet 600mg daily dose(three capsules, 200 mg/capsule)

Sponsors & Collaborators

  • U.S. Army Medical Research and Development Command

    lead FED

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02080767 on ClinicalTrials.gov