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Taking people in FranceNo phase

Measures CALR gene levels in patients with blood cell disorders over time

Checks CALR gene levels in adults with CALR-mutated myeloproliferative disease to track progression.

Key facts

Who runs it
University Hospital, Angers
Where
Angers, Bordeaux, Brest, Cholet, Le Mans, Morlaix, Paris, Poitiers, Quimper, and Tours, FranceSee the 10 sites
Trial code
Registry title
Interest of CALR Allele Burden in Diagnosis and Follow-up of Patients With CALR Mutated Myeloproliferative Syndromes (CALRSUIVI)
Status
Recruiting
People taking part
260 people, planned
Started
28 Oct 2021
Expected to end
28 Apr 2030
Type of study
Interventional
Treatments tested
  • CALR allele burden quantification
Record updated
6 March 2026

Who can take part

AI summary

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults with a myeloproliferative neoplasm that has a CALR gene change, diagnosed between 2006 and 2020, with a stored sample from diagnosis or before treatment.

Age
18 years or older
Sex
All sexes can join
Disease stage
Myeloproliferative neoplasm with a CALR mutation, diagnosed between 2006 and 2020
Earlier treatment
At least one sample must be available from the time of diagnosis or from before treatment to reduce blood cell counts (cytoreductive treatment).
Biomarker or test result
CALR mutation

Main reasons for not taking part

  • Another active blood disease or cancer at the time of diagnosis
  • A person under a legal protection scheme
  • A person who cannot give consent

The registry criteria, word for word

Show all 8 criteriaShow less

Who can take part

  • 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 consent to participate in the study,
  • included, or consenting to be included, in the national clinical-biological database of France Intergroupe Syndrome Myéloprolifératifs (FIM)

Who cannot take part

  • patient with another active hematological disease or cancer at the time of diagnosis,
  • person subject to legal protection scheme or incapable of giving consent

Where in France

  • CHU AngersAngers, FranceContact: Laurane COTTIN, DrTaking people
  • CHU BordeauxBordeaux, FranceContact: Olivier MANSIER, DOCTORTaking people
  • Chu BrestBrest, FranceContact: ERIC LIPPERT, PROFESSORTaking people
  • CH CholetCholet, FranceContact: CHARLES BESCOND, DOCTORTaking people
  • CH Le MansLe Mans, FranceContact: KAMEL LARIBI, DOCTORTaking people
  • CH MorlaixMorlaix, FranceContact: CHRISTOPHE NICOL, DOCTORTaking people
  • AP-HP Henri MondorParis, FranceContact: Lydia ROY, DOCTORTaking people
  • CHU PoitiersPoitiers, FranceContact: Jose Miguel TORREGROSA-DIAZ, DOCTORTaking people
  • CH QuimperQuimper, FranceContact: Lenaig LE CLECH, DOCTORTaking people
  • CHU ToursTours, FranceContact: Olivier HERAULT, PROFESSORTaking people

About the trial

What the trial wants to find out

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

The group in the trial

  • CALRSUIVI cohortTreatment being tested

    Treatment: CALR allele burden quantification

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
Interest of CALR Allele Burden in Diagnosis and Follow-up of Patients With CALR Mutated Myeloproliferative Syndromes (CALRSUIVI)
Plain-language title
Measures CALR gene levels in patients with blood cell disorders over timeGenerated from the registry record. The registry title is the official one.
AI summary
From the trial's eligibility criteria. Read by machine on 12 November 2026.
Record updated
6 March 2026