drugset / Trial / NCT04419649

A Study of Elritercept to Treat Anemia in Adults With Very Low, Low, or Intermediate Risk Myelodysplastic Syndromes (MDS)

NCT04419649

Phase 2 Recruiting 160 enrolled Takeda
Non-randomizedSequentialOpen-labelTreatment

Summary

The main aim of this study is to learn how safe elritercept is and how well adults with anemia associated with lower-risk MDS tolerate treatment with different doses of elritercept. Other aims are to learn how safe elritercept is by looking at how many participants have MDS that worsens during the study and learn about the effects of elritercept on anemia linked to MDS. The study will also look to learn how elritercept affects the production of healthy RBCs.

Timeline

Start
2020-08-19
Primary completion
2029-10-30
Completion
2031-10-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Elritercept Protein / enzyme biologic 0.75 mg/kg Subcutaneous
Subject Elritercept Protein / enzyme biologic 1.5 mg/kg Subcutaneous
Subject Elritercept Protein / enzyme biologic 2.5 mg/kg Subcutaneous
Subject Elritercept Protein / enzyme biologic 3.75 mg/kg Subcutaneous
Subject Elritercept Protein / enzyme biologic 5 mg/kg Subcutaneous