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Not yet recruitingNCT07342829POQS-BoostedUpdated Jan 20, 2026

Prospective Follow-up After MVA-BN Booster Vaccination

An observational study in Monkeypox (Mpox), sponsored by Institute of Tropical Medicine, Belgium. Not yet recruiting at 1 site in Belgium. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-01-20.

Sponsored by Institute of Tropical Medicine, Belgium · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
95
Ages
18 Years and older
Sex
All
01

Study summary

POQS-Boosted is a prospective observational study during which individuals who received Booster vaccination against mpox with the MVA-BN vaccine will be invited to provide biological samples at multiple times over the course of two years.

Read the detailed description

Mpox caused a worldwide outbreak in 2022 and continues to circulate worldwide and causes sporadic cases in Belgium and elsewhere. In the last 10 days, the first cases infected with the probably more virulent clade Ib MPXV have been reported from men who have sex with men in Belgium, the Netherlands, and elsewhere, indicating circulating this viral clade in sexual networks. In Belgium, vaccination against mpox was ceased at the end of 2022 and evidence showed that antibody levels against MPXV have decreased since then, raising questions about sustained protectiveness and the potential for a new mpox outbreak to emerge.

POQS-Boosted is a prospective observational study during which individuals who received Booster vaccination against mpox with the MVA-BN vaccine will be invited to provide biological samples at multiple times over the course of two years.

02

Conditions studied

  • Monkeypox (Mpox)

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Keywords

  • mpox
  • immunology
  • vaccination
  • booster
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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Individuals who received MVA-BN booster vaccination will be asked to participate in "POQS-Boosted"

Inclusion criteria

  1. Is scheduled to receive a booster dose of MVA-BN
  2. ≥18 years
  3. Willingness to provide written informed consent
  4. Willingness to follow the study schedule

Exclusion criteria

Exclusion Criteria:

1. Past or current MPXV infection

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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
95 participants (estimated)
Target follow-up
2 Years
Patient registry
Yes
Biospecimen retention
Samples with dna
05

What researchers measure

Primary outcomes

  1. Orthopoxvirus-specific serum binding and neutralising antibody titre

    To describe the evolution of the orthopoxvirus-specific serum antibody response up to two years after MVA-BN booster vaccination

    Time frame: from enrollment to the end of follow up at 2 years

Secondary outcomes

  1. Orthopoxvirus-specific systemic T- and B cell-mediated immune responses to MPXV

    To describe the evolution of the orthopoxvirus-specific systemic cellular immune response up to two years after MVA-BN booster vaccination

    Time frame: from enrollment up to 2 years

  2. MPXV-specific IgA in saliva and anorectal samples; T and B cell-mediated immune responses to MPXV, measured on saliva and anorectal samples

    To describe the evolution of the orthopoxvirus-specific mucosal antibody \& cellular immune response up to two years after MVA-BN booster vaccination

    Time frame: from enrolment up to two years

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Study locations

1 site
  • Institute of Tropical Medicine
    Antwerp, 2000, Belgium
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References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07342829
Lead sponsor
Institute of Tropical Medicine, Belgium
Responsible party
Sponsor
First posted
Jan 15, 2026
Start date
Jan 15, 2026 (estimated)
Primary completion
Jun 30, 2028 (estimated)
Completion
Jun 30, 2028 (estimated)
Last update
Jan 20, 2026

Study contacts

Christophe Van Dijck, PhD
Contact
cvandijck@itg.be
+32 3 345 58 65
Clinical Trials Unit Antwerp
Contact
studies@itg.be
+32 3 247 66 66
Laurens Liesenborghs, MD
principal investigator · Institute of Tropical Medicine Antwerp

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jan 2026. You cannot join it, but the record below documents what was studied.

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