Vaccine Response Study for Monkeypox

Characterization of Vaccine-induced Responses Against Monkeypox (MoVIHvax) An Observational Prospective Cohort Study

Recruiting Observational Study
Monkeypox
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
100 (estimated)
Sponsor
Fundación FLS de Lucha Contra el Sida, las Enfermedades Infecciosas y la Promoción de la Salud y la Ciencia · Other
Who this trial is looking for

This trial is looking for adults who are at high risk of monkeypox infection and have either HIV or not. Participants will receive a vaccine and help researchers understand how well it works and how the body responds.

Are You a Good Fit for This Trial?

You may be able to join if

  • I am 18 years old or older.
  • I am willing to follow the study's requirements.
  • I understand the information given to me and can give my consent.

You may not be able to join if

  • I have a medical condition that might increase my risks.
  • I have a condition that could interfere with the study.

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial

This observational study has been designed to characterize humoral and cellular immune responses after vaccination against monkeypox (MKP) in HIV positive and negative individuals at high risk of MKP infection during the vaccination campaign in the current monkeypox outbreak.

Trial Locations

Sorted by distance from Idaho

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Eligibility Criteria
Inclusion Criteria: 1. Adult individuals of ≥18 years old. 2. Willing to comply with the requirements of the protocol and available for follow-up for the planned duration of the trial. 3. Has understood the information provided and capable of giving informed consent. Exclusion Criteria: 1\. Parti…
Contacts

Beatriz Mothe, PhD, MD

676142408

bmothe@irsicaixa.es

CONTACT

Susana Benet, PhD, MD

676142408

sbenet@lluita.org

CONTACT