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WithdrawnNo phase

Calprotectin, a Biomarker of COVID-19 Severity (CALPRO)

Key facts

Who runs it
Assistance Publique - Hôpitaux de Paris
Where
France1 site in 1 countryChoose a country to see its sites
Trial code
Status
Withdrawn
Started
Jan 2023
Ended
Jul 2024
Type of study
Interventional, 3 groups
Treatments tested
  • Blood samples
Record updated
12 March 2026
Why it stopped
Abandonment of the study project

Who can take part

Age
18 years and older
Sex
Women and men
Healthy volunteers
Can take part

The registry criteria, word for word

Show all 13 criteriaShow less

Who can take part

  • Criteria for all groups:
  • Adults ≥ 18 years
  • Dated and signed inform consent *; * : written informed consent of relative (trusted person, close family) in case of emergency procedure, by default emergency inclusion notified in medical file and pursuance consent sought
  • Affiliation with a social security scheme; Criteria for control group:
  • Age-matched healthy donors; Criteria for chronic myeloid malignancies:
  • A diagnosis of low or high-risk myelodysplastic syndromes according to the WHO 2016 classification
  • A diagnosis of dysplastic or proliferative chronic myelomonocytic leukemia according to WHO 2016; Criteria for COVID-19 patients:
  • Patients with a recent diagnosis (<7 days since first symptoms) of moderate or severe COVID-19

Who cannot take part

  • Patients with COVID-19 infection and active cancer or a history of cancer within the last 6 months
  • Patients with COVID-19 and severe comorbidities including cardiovascular or respiratory diseases, unbalanced diabetes, obesity (IMC >29)
  • Pregnant women
  • Minor patient or major under protection
  • Patient on AME (state medical aid)

This trial has no sites in United States.

It has sites in one country. Choose a country to see its sites.

About the trial

What the trial wants to find out

The purpose of this study is to provide new insights into the pathophysiology of emergency hematopoiesis detected in severe COVID-19 patients. The investigators aim to explore the ability of calprotectin to induce an immunosuppressive myeloid program at the hematopoietic stem and progenitor cell (HSPC) level, and to identify the receptor(s) involved in this effect. Since patients with a hematological malignancy demonstrate a very high propensity to develop a severe COVID-19, the investigators will explore how HSPCs collected from patients with a myeloid malignancy respond to calprotectin.

The 3 groups in the trial

  • COVID-19 patients (group 1)Treatment being tested

    Patients with a recent diagnosis (\<7 days since first symptoms) of moderate or severe COVID-19

    Treatment: Blood samples

  • Chronic myeloid malignancies (group 2)Treatment being tested

    Adults with chronic myeloid malignancies including myelodysplastic syndromes with low risk MDS ; high risk MDS according to IPSS-R or with dysplastic or proliferative chronic myelomonocytic leukemia according to WHO2016

    Treatment: Blood samples

  • Control group (group 3)Other group

    Age-matched healthy donors

    Treatment: Blood samples

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
Calprotectin Involvement in Emergency Hematopoiesis Observed in Severe COVID-19
Record updated
12 March 2026