European Trial Into Mpox Infection
Recruiting now · Phase 4 · Has a placebo group
Conditions studied: Monkeypox
In brief
The goal of this randomized controlled double-blind clinical trial is to test the drug tecovirimat in patients with mpox (previously known as monkeypox) disease. The main questions it aims to answer are: * Is tecovirimat effective in treating mpox infection. * Is tecovirimat safe to treat patients with mpox infection. Participants will receive either the drug tecovirimat orally, 600 mg twice per day, or a matching placebo. The outcome of the infection and the side effect experienced will be compared between the two groups.
Key facts
- Study ID
- NCT06156566
- Run by
- Miquel Ekkelenkamp
- People needed
- 150
- Starts
- 2024-08-09
- Expected to finish
- 2026-08-01
- Last updated by the study team
- 2025-03-28
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Polymerase Chain Reaction (PCR) /Nucleic Acid Amplification Test (NAAT) -confirmed mpox infection
- The presence of active skin or mucosal lesion(s)
- Signed Informed Consent Form
You may not qualify if…
- Age <18 years.
- Body weight <40 kg
- Pregnant and breastfeeding patients are not eligible for inclusion in this study.
- Lack of mental capacity to provide informed consent
- Trial participation is considered not in the best interest of patient
- Known hypersensitivity to the active substance or to any of the excipients of the study drug.
- Use of contraindicated treatment repaglinide. (Repaglinide, an oral treatment for diabetes mellitus, may be discontinued while taking study treatment with the agreement of the patient's general practitioner, who may start alternate diabetes treatment if considered necessary.)
- Previous, current or planned use of another investigational drug (tecovirimat) at any point during study participation.
- The patient's own doctor considers there to be a definite indication for the patient to receive tecovirimat or the local guidelines establish that tecovirimat treatment should be initiated
- The patient's own doctor considers there to be a definite contraindication to the patient receiving tecovirimat.
- The patient suffers from hereditary problems of galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption.
Where it is running
- Institute of Tropical Medicine — Antwerp, Antwerp, Belgium (enrolling)
- Cliniques Universitaires St. Luc — Brussels, Belgium
- APHP St. Louis — Paris, France
- Universitätsklinikum Bonn — Bonn, Germany
- Hospital Luigi Sacco — Milan, Italy
- Azienda Ospedaliera Universitaria Integrata Verona - AOUI Verona — Verona, Italy
- Amsterdam UMC - AMC — Amsterdam, Netherlands
- Oslo Unversity Hospital — Oslo, Norway
- Hospital de Santo António dos Capuchos — Lisbon, Portugal
- Hospital Clinico San Carlos — Madrid, Spain
- Hospital Universitario La Paz — Madrid, Spain
- Hospital Universitario Virgen Macarena — Seville, Spain
Full record on ClinicalTrials.gov
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