Phase
Condition
Leukemia
Myelodysplastic Syndromes (Mds)
White Cell Disorders
Treatment
Metformin
Clinical Study ID
Ages > 18 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Patients are eligible to be included in WP1 if they meet all of the following criteria:
Inclusion criteria:
A diagnosis of:
LR-MDS according to the revised international prognostic scoring system (IPSS-R), i.e., very low- or low-risk disease (IPSS-R score ≤3) in addition toa bone marrow blast percentage <5 OR
CCUS defined as the presence of somatic mutation(s) or cytogenetic abnormalitynot diagnostic of MDS or any other malignancy in the context of persistentcytopenia (>6 months) with other common causes of cytopenia ruled out in thesetting of bone marrow morphology that is not diagnostic of MDS or any othermalignancy, and hematolytic conditions have been ruled out. Peripheral bloodcytopenia 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, platelet count <150 x 109/L, or neutrophil count <1.8 x 109/L
Menopause, if being a female, defined as females >45 years of age who haveexperienced amenorrhea for minimum 12 months, without any other obvious pathologicalor physiological cause
≥18 years of age
Written informed consent
Willingness to comply with mandatory aspects of the protocol
Ability to swallow pills
Exclusion
Exclusion criteria:
Any prior treatment with metformin
A diagnosis of diabetes mellitus
Therapeutic radiation, immunosuppressive therapy (with the exception ofcorticosteroids), or chemotherapy within the past year
Treatment with granulocyte colony-stimulating factor 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)
An eGFR calculation performed up to one month prior to inclusion may be used to assess renal function. If such an assessment is not available, it is performed at screening.
Healthy volunteers are eligible to be included in WP0 if they meet all of the following criteria:
Inclusion criteria:
Healthy individuals matched on age, sex, and BMI, if possible, to individual patientparticipants in WP1
Written informed consent
Willingness to comply with mandatory aspects of the protocol
Exclusion criteria:
Use of metformin within the past 3 years
A diagnosis of diabetes mellitus, rheumatological disorders, autoimmune diseases orother inflammatory disorders, celiac disease, inflammatory bowel disease, or othergastrointestinal disorders or symptoms
Treatment with immunosuppressive drugs (with the exception of corticosteroids) orchemotherapy within the past year or antibiotics within the past 6 months
Any contraindications to MRS
Study Design
Study Description
Connect with a study center
Rigshospitalet
Copenhagen, Copenhagen N 2200
DenmarkActive - Recruiting
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