NCT04741945RecruitingPhase 2
STOP-LEUKEMIA: Repurposing metformin as a leukemia-preventive drug in CCUS and LR-MDS
Repurposing Metformin as a Leukemia-preventive Drug in CCUS and LR-MDS
Source: EU CTIS (euclinicaltrials.eu) · Last updated 19 Dec 2025
Brief summary (registry, in English)
The purpose of this pilot study is to investigate safety of metformin and feasibility of the study protocol in patients with clonal cytopenia of undetermined significance (CCUS) and lower-risk myelodysplastic syndromes (LR-MDS) and examine potential mechanisms of action of metformin in controlling disease progression in order to inform the design of a future phase 3 randomized controlled trial (RCT) of the efficacy of metformin in CCUS and LR-MDS patients.
- Status (registry)
- Recruiting
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 70 (estimated)
- First submitted
- 20 Dec 2024
- Start date
- 1 Dec 2021
- Lead sponsor
- Rigshospitalet
- Diseases
- Myelodysplastic syndromes
- NCT number
- NCT04741945
- EU CT number
- 2024-518436-37-01
- EudraCT number
- 2020-005088-30
What you commit to
- Study type: Interventional · Phase 2
- Planned participants: 70
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study, not your situation.
Who cannot take part
Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- WP0: • Use of metformin within the past 3 years. • A diagnosis of diabetes mellitus, rheumatological disorders, autoimmune diseases, or other inflammatory disorders, celiac disease, inflammatory bowel disease, or other gastrointestinal disorders or symptoms. • Treatment with immunosuppressive drugs (with the exception of corticosteroids) or chemotherapy within the past year, or antibiotics within the past 6 months. • Any contraindications to magnetic resonance scanning (MRS).
Lab values
- WP1: • Any prior treatment with metformin. • A diagnosis of diabetes mellitus. • Therapeutic radiation, immunosuppressive therapy (with the exception of corticosteroids), or chemotherapy within the past year. • Treatment with G-CSF within the past 30 days. • Prior therapy with hypomethylating agents (i.e., azacitidine, decitabine). • eGFR <45 mL/min. • Performance status according to the Eastern Cooperative Oncology Group >2. • Other active malignancy within the past five years. • Uncontrolled comorbidity including impaired hepatic function (total serum bilirubin >1.5 × upper limit of the normal range (ULN), serum alanine transaminase >3 × ULN), chronic hepatitis with decompensated cirrhosis, disabling psychiatric disease, severe neurologic disease, uncontrolled metabolic disease, or severe cardiac disease (NYHA class 3‐4).
Who the study is looking for
- Work Package (WP) 0: • Healthy individuals matched on age, sex, and BMI, if possible, to individual patient participants in WP1. • Written informed consent prior to study procedures. • Willingness to comply with mandatory aspects of the protocol.
- WP1: • A diagnosis of: o MDS of very low- or low-risk according to the revised international prognostic scoring system (IPSS-R; IPSS-R score ≤3) in addition to a bone marrow blast percentage of <5% OR o CCUS defined as the presence of somatic mutation(s) or cytogenetic abnormality not diagnostic of MDS or any other malignancy in the context of persistent cytopenia (>6 months) with other common causes of cytopenia ruled out in the setting of bone marrow morphology that is not diagnostic of MDS or any other malignancy, and hemolytic conditions have been ruled out. Peripheral blood (PB) cytopenia is defined as hemoglobin (hgb) <11.3 g/dL (7 mmol/L) in women and hgb <12.9 g/dL (8 mmol/L) in men, thrombocytes <150 x 109/L, or neutrophilocytes <1.8 x 109/L. • Menopause, if being a female, defined as females >45 years of age who have experienced amenorrhea for minimum 12 months, without any other obvious pathological or physiological cause. • ≥18 years of age. • Written informed consent prior to study procedures. • Willingness to comply with mandatory aspects of the protocol. • Ability to swallow pills.
Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Rigshospitalet Coordinator of this site? Confirm its status | Copenhagen Oe | Denmark | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.