For Healthcare Professionals

A Study of KER-050 to Treat Anemia Due to Very Low, Low, or Intermediate Risk Myelodysplastic Syndromes

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About the study

The purpose of this study is to evaluate the effects of KER-050 on anemia in patients with very low, low or intermediate risk MDS.
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

Key Inclusion Criteria:

  1. Diagnosis of MDS according to World Health Organization (WHO)/French American British (FAB) classification that meets Revised International Prognostic Scoring System (IPSS-R) classification of very low, low, or intermediate risk disease.
  2. < 5% blasts in bone marrow.
  3. Peripheral blood white blood cell count <13,000/µL.

Anemia defined as:

  1. In non-transfused participants, having received no red blood cell (RBC) transfusions within 8 weeks Hgb concentration ≤ 10.0 g/dL OR
  2. In LTB participants, having received 1 to 3 units RBCs for Hgb ≤ 9.0 g/dL within 8 weeks OR
  3. In HTB participants, having received ≥ 4 units of RBCs for Hgb ≤ 9.0 g/dL within 8 weeks
  4. Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2 (if related to anemia.
  5. Females of child-bearing potential and sexually active males must agree to use effective methods of contraception.

EXCLUSION CRITERIA

Key Exclusion Criteria:

  1. Any active infection requiring parenteral antibiotic therapy within 28 days prior to Cycle 1 Day 1 or oral antibiotics within 14 days of Cycle 1 Day 1.
  2. Diagnosis of secondary MDS (i.e., MDS known to have arisen as the result of chemical injury or treatment with chemotherapy and/or radiation for other diseases).
  3. Vitamin B12 deficiency.
  4. Prior treatment with azacitidine, decitabine, lenalidomide, luspatercept, or sotatercept.

Treatment within 28 days prior to Cycle 1 Day 1 with:

  1. Erythropoiesis stimulating agent (ESA) OR
  2. Granulocyte colony-stimulating factor (G-CSF) OR
  3. Granulocyte-macrophage colony-stimulating factor (GM-CSF)
  4. Iron chelation therapy if initiated within 8 weeks prior to Cycle 1 Day 1.
  5. Vitamin B12 therapy within 8 weeks prior to Cycle 1 Day 1.
  6. Treatment with another investigational drug or device or approved therapy for investigational use < or = 28 days prior to Cycle 1 Day 1, or if the half-life of the previous product is known, within 5 times the half-life prior to Cycle 1 Day 1, whichever is longer.
  7. Platelet count > 450 x 10*9/L or < 30 x 10*9/L.
  8. Transferrin saturation < 15%.
  9. Ferritin < 50 µg/L.
  10. Folate < 4.5 nmol/L (< 2.0 ng/mL).
  11. Vitamin B12 < 148 pmol/L (< 200 pg/mL).
  12. Estimated glomerular filtration rate (GFR) < 40 mL/min/1.73 m2 (as determined by the Chronic Kidney Disease Epidemiology Collaboration [CKD-EPI].
  13. Pregnant or lactating females
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Study Locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.
Phone iconCall +1 (617) 314-6297Email iconEmail Study Center

Study’s details


Contition

Myelodysplastic Syndromes,Cytopenia

Age (in years)

18+

Phase

Phase 2

Participants needed

140

Est. Completion Date

Nov 30, 2025

Treatment type

Interventional


Sponsor

Keros Therapeutics, Inc.

ClinicalTrials.gov identifier

NCT04419649

Study number

KER050-MD-201

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