An observational study in Clonal Hematopoiesis, Clonal Hematopoiesis of Indeterminate Potential and Clonal Cytopenia of Undetermined Significance (CCUS), sponsored by VASCage GmbH. Not yet recruiting at 1 site in Austria. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-21.
Sponsored by VASCage GmbH · Observational
Clonal hematopoiesis (CH), including clonal hematopoiesis of indeterminate potential (CHIP), is an age-associated condition characterized by the expansion of hematopoietic stem and progenitor cell clones carrying acquired somatic mutations. Although CH is associated with an increased risk of hematologic malignancies, its greater public health impact derives from its strong association with cardiovascular diseases, including coronary artery disease and stroke. Emerging evidence suggests that CH-associated mutations promote chronic inflammatory signaling in myeloid immune cells, thereby contributing to atherosclerosis and adverse cardiovascular remodeling.
This observational translational study aims to characterize the biological spectrum of clonal hematopoiesis across different stages of disease risk and manifestation. Using state-of-the-art single-cell and multi-omics approaches, the study will compare inflammatory pathways, immune cell states, and mutation-associated molecular programs among healthy individuals without CH, individuals with high-risk CH, and patients with CH-associated hematologic or cardiovascular disease. The ultimate goal is to identify shared and disease-specific mechanisms linking clonal hematopoiesis to adverse clinical outcomes and to generate insights for future preventive, anti-clonal, and anti-inflammatory therapeutic strategies.
Background and Rationale:
Clonal hematopoiesis (CH), including clonal hematopoiesis of indeterminate potential (CHIP), arises from acquired somatic mutations in hematopoietic stem and progenitor cells that accumulate throughout life and drive clonal expansion. The most frequently affected genes include DNMT3A, TET2, and ASXL1. While such mutations are also involved in the pathogenesis of hematologic malignancies such as myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML), progression to overt hematologic cancer occurs only in a minority of affected individuals.
In contrast, epidemiological studies have consistently demonstrated a strong association between clonal hematopoiesis and cardiovascular disease. Individuals carrying CHIP-associated mutations have a substantially increased risk of coronary artery disease, myocardial infarction, stroke, and cardiovascular mortality. The magnitude of risk conferred by CHIP has been reported to be comparable to established cardiovascular risk factors such as smoking or hypertension.
Experimental and mechanistic studies suggest that CH-associated mutations remodel immune-cell function through epigenetic reprogramming and activation of inflammatory pathways, including the NLRP3 inflammasome and cGAS-STING signaling. These alterations enhance the proliferation, activation, and inflammatory potential of myeloid immune cells, resulting in chronic sterile inflammation that can promote atherosclerosis, vascular injury, and adverse cardiac remodeling.
Importantly, clonal hematopoiesis is not considered a disease entity itself but rather a common biological state and independent risk factor for a range of age-related disorders. Since clonal hematopoiesis develops in varying degrees in a substantial proportion of the aging population, understanding its biological consequences represents a major opportunity for disease prevention.
Additional support for a causal role of inflammation comes from retrospective analyses of the CANTOS trial, which suggested that individuals carrying somatic TET2 mutations derived particularly strong benefit from anti-inflammatory treatment targeting interleukin-1β. These findings highlight the potential for precision prevention and targeted therapeutic interventions in CH-associated disease. However, a more comprehensive understanding of the cellular and molecular mechanisms linking clonal hematopoiesis to disease development is required for improved risk stratification and the development of novel therapeutic approaches.
Study Objectives:
The primary objective of this study is to define the inflammatory and immunological landscape across the biological continuum of clonal hematopoiesis, from healthy individuals without detectable CH to individuals with high-risk CH and patients with CH-associated hematologic or cardiovascular disease.
Specific objectives include:
Study Design:
This is a prospective observational translational research study.
A total of six participant groups will be recruited, with approximately 20 participants per group (total n ≈ 120). The groups will represent different stages along the spectrum of clonal hematopoiesis and disease manifestation, including:
Study Procedures:
Participants will provide peripheral whole-blood samples for comprehensive molecular, cellular, and functional analyses. Planned investigations include:
Expected Impact:
The study is designed to establish a comprehensive map of inflammatory and immune mechanisms associated with clonal hematopoiesis across its natural history. By defining the biological pathways that connect somatic mutations to hematologic and cardiovascular disease, the project aims to support the development of improved risk stratification tools and enable future preventive, anti-clonal, and anti-inflammatory therapeutic strategies. Ultimately, these efforts may contribute to preventing or delaying progression from healthy aging through clonal hematopoiesis to clinically manifest hematologic and cardiovascular disease.
1,997 studies on the registry are indexed under Myelodysplastic Syndromes; 324 are open to participants now.
This study's planned enrollment of 120 is below the median of 150 across 214 observational studies indexed under Myelodysplastic Syndromes.
Browse Myelodysplastic Syndromes studies →VASCage GmbH is the lead sponsor of 12 studies on the registry; 6 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Adults aged ≥60 years will be recruited across six predefined cohorts representing the continuum from healthy aging to clonal hematopoiesis-associated hematologic and cardiovascular disease. The study population includes healthy controls, individuals with low-risk and intermediate/high-risk clonal hematopoiesis, patients with clonal cytopenia of undetermined significance (CCUS), patients with low-risk myelodysplastic syndrome (MDS), and patients with recent ST-segment elevation myocardial infarction (STEMI).
Inclusion Criteria: Participants must be ≥18 years of age and meet at least one of the following criteria:
Group A: Control Group (n=20)
Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
The protein in red blood cells that carries oxygen. A low level is anaemia, which can cause tiredness and breathlessness. Measured in g/dL or g/L (9 g/dL is 90 g/L).
The number of neutrophils, white blood cells that help fight infection, in a given amount of blood. Too few raises the risk of infection.
It is a count, not a percentage of the white cells. Limits are written in units that mean the same: ≥ 1.5 × 10⁹/L is ≥ 1,500 per mm³ (µL). Each lab has its own reference range.
Blood cells that help blood clot. Too few raises the risk of bleeding and bruising. A usual adult range is about 150–400 × 10⁹/L (150,000–400,000 per µL); each lab has its own reference range.
A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.
Read whether the line is about a condition or about medicines, and which medicines and doses it means.
Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.
Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.
A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.
Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Hemoglobin (Hb)
The protein in red blood cells that carries oxygen. A low level is anaemia, which can cause tiredness and breathlessness. Measured in g/dL or g/L (9 g/dL is 90 g/L).
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Absolute neutrophil count (ANC)
The number of neutrophils, white blood cells that help fight infection, in a given amount of blood. Too few raises the risk of infection.
It is a count, not a percentage of the white cells. Limits are written in units that mean the same: ≥ 1.5 × 10⁹/L is ≥ 1,500 per mm³ (µL). Each lab has its own reference range.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Platelets
Blood cells that help blood clot. Too few raises the risk of bleeding and bruising. A usual adult range is about 150–400 × 10⁹/L (150,000–400,000 per µL); each lab has its own reference range.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Immunosuppression
A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.
Read whether the line is about a condition or about medicines, and which medicines and doses it means.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Corticosteroids (steroids)
Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.
Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Autoimmune disease
A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.
Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Participants aged ≥60 years without detectable clonal hematopoiesis-associated somatic variants, no history of myocardial infarction or stroke, no cytopenia, no WHO-defined neoplasm, and no major surgery within the previous 3 months.
Participants aged ≥60 years with clonal hematopoiesis carrying a somatic mutation in DNMT3A, TET2, ASXL1, or JAK2 (variant allele frequency ≥2%), no prior cardiovascular events, no cytopenia, no WHO-defined neoplasm, and a low Clonal Hematopoiesis Risk Score (CHRS \<9.5).
Participants aged ≥60 years with clonal hematopoiesis carrying a somatic mutation in DNMT3A, TET2, ASXL1, or JAK2 (variant allele frequency ≥2%), no prior cardiovascular events, no cytopenia, no WHO-defined neoplasm, and an intermediate or high Clonal Hematopoiesis Risk Score (CHRS \>9.5).
Participants aged ≥60 years with clonal hematopoiesis-associated mutations and persistent unexplained cytopenia for at least 4 months who do not meet diagnostic criteria for a myeloid neoplasm based on bone marrow evaluation.
Participants aged ≥60 years with clonal hematopoiesis-associated mutations and a recent ST-segment elevation myocardial infarction (STEMI) treated with percutaneous coronary intervention within the previous 4 months, without prior stroke, coronary artery bypass graft surgery, cytopenia, or WHO-defined neoplasm.
Participants aged ≥60 years with newly diagnosed (\<3 months), untreated lower-risk myelodysplastic syndrome defined by an IPSS-R score \>1.5 to 3 points and no history of myocardial infarction or stroke.
Inflammatory transcriptional profile of mutation-bearing immune cells
Single-cell gene expression differences in predefined inflammatory pathways (including NLRP3 inflammasome, interferon signaling, and cGAS-STING-related pathways) between immune cells with and without clonal hematopoiesis-associated somatic variants and across study groups.
Time frame: Baseline
Plan to share: Undecided
No publications or documents are linked to this record.
Start is estimated for Oct 2026; primary completion for Mar 2027, 5 months later.
How these figures are worked out, and which studies are left out of them.
This study is not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.
Get an email when the registry record changes — status, dates, results — or when someone posts here.
Sign in to followQuestions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.
Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.
Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.
VASCage GmbH