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2023-504519-34-01CompletedPhase 2

Using live vaccines to induce beneficial innate immune training and reduce systemic inflammation in COPD patients

Using live vaccines to induce beneficial innate immune training and reduce systemic inflammation in COPD patients (COPD-LIVE)

Source: EU CTIS (euclinicaltrials.eu) · Last updated 23 Apr 2024

Next steps

Brief summary (registry, in English)

To characterize the changes in the innate immune system of COPD patients upon vaccination with live vaccines and determine if vaccination induces trained immunity as reported previously in other populations.

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
60 (actual)
First submitted
18 Oct 2023
Start date
22 Feb 2024
Lead sponsor
Gentofte Hospital
Diseases
COPD
EU CT number
2023-504519-34-01

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 60
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study design.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Oral or intravenous corticosteroid at a dose ≥10 mg/day over 3 months
  • Known allergy to either the BCG or MMR vaccines or severe adverse effects during prior vaccination.
  • Known prior, active or latent infection with mycobacterium tuberculosis.
  • Vaccination with a live vaccine within 4 weeks

Other illness

  • Cardiac arythmia
  • Allergy to MMR vaccine components, neomycin or egg proteins.
  • Severe immunocompromisation (HIV-1 infection, organ- or bone marrow transplantation, chemotherapy, primary immune defect, anti-cytokine therapy, immunosuppressant treatment).
  • Active solid or non-solid malignancy or lymphona within 2 years, excluding basal cell carcinoma

Other

  • Acute febrile ilness
  • Blood dyscrasia
  • Pregnancy or breastfeeding

Who the study is looking for

  • Must have specialist verified, spirometry-confirmed, COPD.
  • Age > 40 years
  • Able to give informed consent

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Gentofte HospitalHellerupDenmarkCompleted

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This page is information, not medical advice. Discuss any trial with your doctor.