Monkeypox vaccine safety under the microscope in congo study

NCT ID NCT05734508

First seen Jun 24, 2026 · Last updated Jun 24, 2026

Summary

This completed study monitored the safety of the MVA-BN (Jynneos) vaccine in 500 adults at high risk for monkeypox in the Democratic Republic of the Congo. Participants received two doses of the vaccine and were followed for up to 28 days after their last dose. The main goal was to track any serious or minor side effects that occurred shortly after vaccination.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Locations

  • Institut National de Rescherche Biomédicale (INRB)

    Kinshasa, Democratic Republic of the Congo

  • L'Hôpital Général de Référence de Kole

    Kole, Democratic Republic of the Congo

  • L'Hôpital Général de Référence de Tunda

    Tunda, Democratic Republic of the Congo

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance

MVA-BN (Jynneos) vaccine

What this could lead to

If the vaccine is shown to be safe, it could support its use to protect people at high risk for monkeypox.

What could go wrong

This study only looked at safety, not how well the vaccine prevents infection. It was also small and limited to a specific group of adults.

Conditions

The condition(s) this trial relates to.

monkeypox

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.