Skip to content

Cohort of Patients With Chronic Myelomonocytic Leukemia

Cohort of Patients With Chronic Myelomonocytic Leukemia

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07512882
Acronym
MYELOMONO-3
Enrollment
5000
Registered
2026-04-06
Start date
2026-05-05
Completion date
2040-03-01
Last updated
2026-05-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Leukemia, Myelomonocytic Leukemia, Chronic

Brief summary

A prospective, non-interventional study involving the collection of biological samples with associated anonymised data. Biological samples will be collected at the time of diagnosis and/or as the disease progresses, with or without treatment, always in conjunction with tests scheduled as part of routine care or within the context of a clinical trial.

Interventions

BIOLOGICALSampling

Blood samples taken as part of a scheduled assessment within the context of medical care * Standard sample: 2 x 10 mL EDTA tubes * For the initial assessment: 1 x 10 mL dry tube At the request of the research teams: one EDTA tube may be replaced by a heparinised or citrated tube, depending on the planned research. Bone marrow samples, taken during a scheduled myelogram as part of medical care * Myelogram: 1 x 2 mL EDTA tube In exceptional cases, during a scheduled surgical procedure, a tissue sample will be considered in consultation with the surgeon (affected tissue, surrounding healthy tissue).

Sponsors

Gustave Roussy, Cancer Campus, Grand Paris
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults aged 18 years and over * Blood monocytosis ≥ 0.5 × 10⁹/L and ≥ 10% of total white blood cells or * Confirmed diagnosis of chronic myelomonocytic leukemia * Regardless of stage (chronic or transformed), and whether or not currently being treated * Signed informed consent

Exclusion criteria

* Active, uncontrolled infection (particularly hepatitis B, hepatitis C, HIV) * Refusal informed consent

Design outcomes

Primary

MeasureTime frameDescription
Understanding the pathophysiology of chronic myelomonocytic leukaemiathrough study completion, an average of 15 yearsoptimise diagnosis, improve prognostic stratification, identify new treatment options and assess patients' response to proposed treatments through the analysis of blood or bone marrow samples collected as part of routine care or clinical trials

Countries

France

Contacts

CONTACTChristophe WILLEKENS
Christophe.willekens@gustaveroussy.fr+33 1 42 11 23 79
CONTACTEric SOLARY
Eric.solary@gustaveroussy.fr+33 1 42 11 67 26

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 20, 2026