CALR Allele Burden for Myeloproliferative Neoplasms

Interest of CALR Allele Burden in Diagnosis and Follow-up of Patients With CALR Mutated Myeloproliferative Syndromes (CALRSUIVI)

Recruiting N/A Interventional Study
Myeloproliferative Neoplasm Essential Thrombocythemia Primary Myelofibrosis, Prefibrotic Stage Primary Myelofibrosis, Fibrotic Stage
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
Ready to participate?

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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Other
Participants needed
260 (estimated)
Sponsor
University Hospital, Angers · Government
Who this trial is looking for

This trial is looking for adults with a specific type of blood cancer called CALR mutated myeloproliferative neoplasm. Participants will be monitored to see how their condition progresses and must provide consent to join.

Are You a Good Fit for This Trial?

You may be able to join if

  • I am at least 18 years old
  • I am part of the national social security system
  • I have been diagnosed with CALR mutated myeloproliferative neoplasm between 2006 and 2020
  • I have at least one sample available from my diagnosis or before treatment
  • I have signed consent to participate
  • I consent to be included in the national clinical-biological database

You may not be able to join if

  • I have another active hematological disease or cancer
  • I am under a legal protection scheme or unable to give consent

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.

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About This Trial

Prospective study to evaluate the relevance of CALR allele burden monitoring as a molecular marker of disease progression.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * adults (age ≥18 years), * affiliated to the national social security system, * with CALR mutated myeloproliferative neoplasm diagnosed between 2006 - 2020, * for which at least one sample is available at the time of diagnosis or before cytoreductive treatment, * who signed the…
Contacts

Laurane COTTIN, Doctor

+33 2 41 35 53 53

Laurane.Cottin@chu-angers.fr

CONTACT

Emma BLANCHET

+33 2 41 35 63 38

EmBlanchet@chu-angers.fr

CONTACT