Study of the safety and effectiveness of Tecovirimat for the treatment of Human MonkeyPox Virus Disease (STOMP)
Lay Description
To determine the difference in time to recovery and healing of monkey pox lesions between people receiving Tecovirimat and those receiving placebo. People with severe cases of monkeypox will receive Tecovirimat and not placebo.
Category
- Skin Conditions
- IRB Number
- 20220654HU
- NCT Number
- NCT # not yet entered
Eligibility
- Eligible Ages
- 18-99
- Eligible Genders
- All
- Accepts Healthy Volunteers
Inclusion Criteria
Illness < 14 days before study entry, have at least 1 active (not scabbed) lesion
Exclusion Criteria
Illness < 14 days before study entry, have at least 1 active (not scabbed) lesion
Study Design
Arm Groups
Study Contact
Irma Scholler
210-450-3150
scholler@uthscsa.edu
Principal Investigator
Thomas Patterson