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A Study to Assess Luspatercept in Lower-risk Myelodysplastic Syndrome Participants

Active, not recruiting · Phase 3 · NCT06045689

Conditions: Myelodysplastic Syndromes

At a glance

Research payments reported, 2025
$1.2M
U.S. investigators named
20
Sites paid
19
Planned or actual enrollment
106

About the trial

Sponsor
Bristol-Myers Squibb
Tested
Luspatercept (drug)
Dates
Started 2023-10-05; completion 2027-09-29
Results posted
Not yet

The purpose of this study is to evaluate the efficacy and safety of Luspatercept when administered at the maximum approved dose in low-risk Myelodysplastic Syndrome participants who require red blood cell transfusions.

From ClinicalTrials.gov, last updated 2026-06-15. Full record, eligibility and contacts (opens in a new tab)

Industry funding

E.r. Squibb & Sons, L.l.c. reported $1.2M in research payments for this study in 2025 (24 payments).

Products named: Reblozyl

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.