Clinical Research Directory

Subjects must meet all of the following inclusion criteria: 1. They must be able to understand the study procedures, comply with them, and consent in writing prior to any specific study procedure. 2. Must be able to understand the study procedures, comply with them, and give written informed consent prior to any study-specific procedure. 3. Adult subjects ≥ 18 years of age with a diagnosis of myelodysplastic syndrome. 4. Very low, low or intermediate IPSS-R risk category. 5. Subject requires are red blood cell transfusion dependent with the following criteria: requires an average of 2 to 6 units of CH on average over an 8-week period. 6. ECOG 0-3. Exclusion criteria 1. Subject undergoing any of the following treatments: azacitidine, decitabine, venetoclax, cytotoxic chemotherapy, radiotherapy, arsenic trioxide, interferon or interleukin. 2. High or very high IPSS-R risk category. 3. Subject diagnosed with any active neoplasm except: * epidermoid or basal cell carcinoma, * carcinoma in situ of the uterine cervix * Carcinoma in situ of the breast 4. Subjects with a score on the New York Heart Association Scale IV. 5. Subjects with major surgery within 8 weeks prior to study inclusion. Subjects must have fully recovered from any previous surgery prior to inclusion in the study. 6. Subject with known clinically significant anaemia due to iron, vitamin B12 or folate deficiencies or autoimmune or hereditary haemolytic anaemia or uncontrolled hypothyroidism or known clinically significant haemorrhage or sequestration or subject with drug induced anaemia. 7. New onset or uncontrolled seizures. 8. Subjects with uncontrolled systemic fungal, bacterial or viral infections (defined as ongoing signs or symptoms related to the infection without improvement despite appropriate antibiotics or antimicrobial therapy). 9. Pregnant or breastfeeding women. 10. The subject has any condition, including the presence of laboratory abnormalities that would place the subject at unacceptable risk if he/she were to participate in the study. 11. The subject has any condition or receives concomitant medication that confounds the ability to interpret the study data.