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RecruitingNCT06462664EMYNEMUpdated Jun 17, 2024

Exploring the Impact of Monocytes in Myeloproliferative Neoplasia (EMYNEM)

An observational study in Myeloproliferative Neoplasm, sponsored by University Hospital, Brest. Recruiting at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-06-17.

Sponsored by University Hospital, Brest · Observational

From the registry’s dates

  • Started Jun 2024; still recruiting 2 years 4 months later.
Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
10
Ages
18 Years and older
Sex
All
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Study summary

Impact of monocytes on Myeloproliferative Neoplasm hematopoietic stem cell growth and differentiation in vitro

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Conditions studied

  • Myeloproliferative Neoplasm
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In context

Myeloproliferative Disorders

626 studies on the registry are indexed under Myeloproliferative Disorders; 109 are open to participants now.

This study's planned enrollment of 10 is below the median of 136 across 108 observational studies indexed under Myeloproliferative Disorders.

Browse Myeloproliferative Disorders studies →

Lead sponsor

University Hospital, Brest is the lead sponsor of 594 studies on the registry; 135 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Sampling method
Non-probability sample

Study population

Patients with MPN

Inclusion criteria

  • Diagnosis of MPN in the participating center
  • Over 18 yo

Exclusion criteria

Exclusion Criteria:

  • Not able to consent
05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
10 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Proliferation and differentiation of hematopoitic stem/progenitor cells

    Time frame: 2 years

07

Study locations

1 of 1 sites recruiting
  • Chu Brest
    Brest, 29609, France
    Recruiting
08

References and documents

Individual participant data

Plan to share: Yes — All collected data that underlie results in a publication

Supporting information: Study protocol

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 17, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06462664
Lead sponsor
University Hospital, Brest
Responsible party
Sponsor
First posted
Jun 17, 2024
Start date
Jun 1, 2024
Primary completion
Jan 31, 2028 (estimated)
Completion
Jan 31, 2028 (estimated)
Last update
Jun 17, 2024

Study contacts

Eric LIPPERT
Contact
eric.lippert@chu-brest.fr
0298347033 ext. +33
Wayne Corentin LAMBERT
Contact
wayne-corentin.lambert@chu-brest.fr

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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