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Myeloproliferative Neoplasm (MPN)NCT07590986

Identification of MPN-specific Antigens and Anti-MPN TCRs in Myeloproliferative Neoplasm

An observational study of Myeloproliferative Neoplasm (MPN) and Polycytemia Vera, run by Université Catholique de Louvain at 1 site in Belgium.

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Sites and contacts
Official record

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Trial summary

The goal of this observational study is to learn how the immune system responds to myeloproliferative neoplasms (MPN) in adults with known or suspected MPN. Researchers also want to identify immune cells that could help develop future immune-based treatments for MPN. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
How many people
150 participants
Where
1 siteBelgium
Study dates
May 2026to Jan 2037
Phase
Observational

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: (i) Adult patients previously diagnosed with or suspected of having PV, ET, pre-PMF, overt PMF, or an unclassifiable MPN. (ii) Healthy controls undergoing hip replacement surgery, that have not been diagnosed with any hematological disease.

Who may be able to join

  • Patients previously diagnosed or suspected of having PV, ET, pre-PMF, overt PMF, or an unclassifiable MPN.
  • Patients not previously diagnosed with a haematological disease as controls

Who cannot join

  • Patients with any other hematological malignancy.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Belgium1 site, 1 recruiting
  • de Duve Institute, UCLouvain

    Brussels, Woluwe, 1200

    Sophie Lucas, Pr, 0032 (0)2 436 23 00, sophie.lucas@uclouvain.be

    Violaine Havelange

    Recruiting

Other trials in Belgium

About this study

The goal of this observational study is to learn how the immune system responds to myeloproliferative neoplasms (MPN) in adults with known or suspected MPN. Researchers also want to identify immune cells that could help develop future immune-based treatments for MPN.

The main questions it aims to answer are:

Read more
  • Are there T cells in the bone marrow that can recognize MPN cells?
  • Which targets (antigens) on MPN cells are recognized by these immune cells?
  • Can researchers identify T cell receptors (TCRs) that may be used in future TCR-based therapies?

Researchers will study samples from adults with polycythemia vera (PV), essential thrombocythemia (ET), primary myelofibrosis (PMF), post-PMF, or unclassifiable MPN. Samples from healthy donors without blood disorders will also be included for comparison.

By providing blood and bone marrow samples, participants will:

  • Allow researchers to study immune cells and genetic material from these samples
  • Allow researchers to perform laboratory tests to study how immune cells recognize MPN cells

Researchers will use laboratory methods such as genetic sequencing, cell analysis, and cell culture experiments to better understand immune responses in MPN.

Participants will not receive direct medical benefit from this study. The results may help researchers better understand MPN and support the future development of immune-based therapies.

Medical subject headings
Myeloproliferative Disorders, Thrombocythemia, Essential, Primary Myelofibrosis

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Identification of MPN-specific CD8+ T cell clonotypes and corresponding tumor antigens

    Measured: Throughout the whole study, approximately during 10 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 May 2026
  2. Study startMay 2026 (estimated)
  3. Primary completionDec 2036 (estimated)
  4. Study completionJan 2037 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case only
Time perspective
Prospective
Enrolment
150 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07590986
Sponsor's protocol ID
MPN-TCR
Status last verified
May 2026
First submitted
8 May 2026
Last updated
15 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

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