A Study to Evaluate Treatment Patterns and Effectiveness of Luspatercept

NCT06971185 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 430

Last updated 2025-05-14

No results posted yet for this study

Summary

The purpose of this study is to understand the treatment patterns and clinical outcomes of myelodysplastic syndromes patients treated with luspatercept or erythropoiesis-stimulating agents

Conditions

  • Myelodysplastic Syndromes (MDS)

Interventions

DRUG

Luspatercept

As per product label

DRUG

Erythropoiesis-stimulating agent (ESA)

As per product label

Sponsors & Collaborators

Principal Investigators

  • Bristol Myers Squibb · Bristol-Myers Squibb

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-11-22
Primary Completion
2025-08-01
Completion
2025-08-01
FDA Drug
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06971185 on ClinicalTrials.gov