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Coverage: 2020-01-01 onwards, with up to 300 results per query from PubMed and Europe PMC and separate limits on other sources. This is a selected index, not a complete literature search.

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ICD C93.1ORPHA:98823CMML

Chronic Myelomonocytic Leukaemia

Chronic myelomonocytic leukaemia is a rare cancer of the blood and bone marrow that mainly affects older adults. It causes a persistently high number of a type of white blood cell called monocytes, and can lead to anaemia, infections, bruising and an enlarged spleen. Treatment ranges from careful monitoring to medicines that act on the bone marrow. Stem cell transplant is an option for some people.

This overview is general information, not an individual medical assessment. Research is selected automatically and may include mismatches. How we select and explain research.

377
Articles
282
Trials (17 AU)
Data refreshed
20 October 2026
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Common Questions

What is Chronic Myelomonocytic Leukaemia?

Chronic myelomonocytic leukaemia is a rare cancer of the blood and bone marrow that mainly affects older adults. It causes a persistently high number of a type of white blood cell called monocytes, and can lead to anaemia, infections, bruising and an enlarged spleen. Treatment ranges from careful monitoring to medicines that act on the bone marrow. Stem cell transplant is an option for some people.

How many clinical trials are available for Chronic Myelomonocytic Leukaemia?

RareWays currently indexes 282 clinical trials for Chronic Myelomonocytic Leukaemia, of which 51 are actively recruiting. These counts cover indexed trials across countries, not just your country. An Australian site does not necessarily mean that site is recruiting. Check locations, eligibility and current availability with the study team.

Where does the research data for Chronic Myelomonocytic Leukaemia come from?

RareWays aggregates research from PubMed, Europe PMC, OpenAlex, and ClinicalTrials.gov. Data is refreshed automatically every day. All articles and trials link directly to their original sources.

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