Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING Phase 3

A Study to Compare Elritercept With Epoetin Alfa to Treat Anemia in Adults With Very Low, Low, or Intermediate Risk Myelodysplastic Syndromes (MDS) Who Need Regular Blood Transfusions

NCT07422480 · View on ClinicalTrials.gov ↗

Study Summary

The main aim of this study is to assess how elritercept works in lowering the need for RBC (red blood cell) transfusions and how safe elritercept is when compared with epoetin alfa. Other aims are to learn if elritercept improves tiredness as reported by participants without needing RBC transfusion compared with epoetin alfa, the RBC transfusion burden and quality of life compared with epoetin alfa. The study also aims to find out the extent of the immune response to elritercept. The study will also check on the medical problems (safety) of elritercept.

Interventions

  • DRUG Elritercept
  • DRUG Epoetin Alfa

Study Locations (20)

Texas

  • World Research Link — Baytown
  • The Center for Cancer and Blood Disorders — Fort Worth
  • The University of Texas-MD Anderson Cancer Center - Leukemia Center — Houston

Tennessee

  • Tennessee Oncology, PLLC — Nashville
  • Vanderbilt University Medical Center — Nashville

California

  • Hematology-Oncology Medical Group of Orange County, Inc - Orange - 1010 W. La Veta Avenue — Orange

Florida

  • BRCR Medical Center Inc — Tamarac

Georgia

  • Emory University — Atlanta

Illinois

  • Orchard Healthcare Research Inc. (OHR) - Skokie — Skokie

Kentucky

  • Norton Cancer Institute — Louisville

Missouri

  • American Oncology Partners P.A. MidAmerica Cancer Care — Kansas City

Trial Details

FieldValue
Enrollment Target 300 participants
Start Date 2026-04-01
Est. Completion 2033-10-01
Phase Phase 3

Sponsor

Takeda

387 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07422480

The ClinicalTrials.gov registry entry for NCT07422480 describes a study currently listed as recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 300 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Takeda, which has 387 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Myelodysplastic Syndrome appearing as the primary indexed condition, and to 2 interventions — of which Elritercept is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT07422480 reports 20 study locations spanning 17 distinct geographic areas — top geographies include Texas, Tennessee, California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT07422480 about?

NCT07422480 is a clinical study titled "A Study to Compare Elritercept With Epoetin Alfa to Treat Anemia in Adults With Very Low, Low, or Intermediate Risk Myelodysplastic Syndromes (MDS) Who Need Regular Blood Transfusions". The main aim of this study is to assess how elritercept works in lowering the need for RBC (red blood cell) transfusions and how safe elritercept is when compared with epoetin alfa. Other aims are to learn if elritercept improves tiredness as reported by participants without needing RBC transfusion ...

What is the current status of trial NCT07422480?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 300 participants. The study started on 2026-04-01. Estimated completion is 2033-10-01.

What conditions does trial NCT07422480 study?

This clinical trial studies the following conditions: Myelodysplastic Syndrome, Anemia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07422480?

The interventions under investigation include: Elritercept (DRUG), Epoetin Alfa (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07422480?

This trial is sponsored by Takeda, which has 387 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07422480 being conducted?

This trial has 20 study locations across California, Florida, Georgia, Illinois, Kentucky. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial