KER-050-D301

A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Elritercept (KER-050) for the Treatment of Transfusion-Dependent Anemia in Adult Participants With Very Low-, Low-, or Intermediate-Risk Myelodysplastic Syndromes (MDS) (RENEW)

AML-MDSNCT06499285Last updated: 2/25/2026
Recruiting

Study Design

Study Drug

Elritercept/ placebo

Mechanism of Action

tgf-β ligand

Sponsor

Unknown

Design

III

Control Arm

-

Criteria

Inclusion Criteria

very low-, low-, intermediate risk MDS, Transfusion dependence assess in 16wks(1U/8weeks), EPO>200, <500.

Age: ≥18 years Phase: III

Exclusion Criteria

Del (5q) MDS or secondary MDS, history of malignancy>=5years, Transplantation, acute infection,

Enrollment

Progress0 / 2

Contact Information

Principal Investigator

陳彩雲

Study Nurse

李佳玲

Contact Tel

4620