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NCT05925504

The Tapering Dose of Luspatercept in Patients With Lower-risk Myelodysplastic Syndromes

Recruiting now Phase 2 Last updated 12 March 2024
What this trial tests

Phase 2 trial testing Luspatercept in Lower Risk MDS Per IPSS-R in 36 participants. Currently enrolling.

Timeline
1 July 2023
Primary endpoint
30 June 2026
30 September 2026

Quick facts

Lead sponsorInstitute of Hematology & Blood Diseases Hospital, China
PhasePhase 2
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment36
Start date1 July 2023
Primary completion30 June 2026
Estimated completion30 September 2026
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Institute of Hematology & Blood Diseases Hospital, China

Who can join

18 and older, any sex, with Lower Risk MDS Per IPSS-R. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a prospective, single center, single-arm, phase 2 study. The aim of this study is to evaluate the efficacy and safety of Luspatercept for Patients with Lower-risk Myelodysplastic Syndromes (MDS).

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Targeting transforming growth factor beta signaling in metastatic osteosarcoma.
    Ge R, Huang GM. · · 2023 · cited 25× · PMID 38021074 · DOI 10.1016/j.jbo.2023.100513
  2. Bone marrow microenvironment in myelodysplastic neoplasms: insights into pathogenesis, biomarkers, and therapeutic targets.
    Bahmani F, Shayanmanesh M, Safari M, Alaei A, et al · · 2025 · cited 3× · PMID 40349084 · DOI 10.1186/s12935-025-03793-z

Verify or expand the search:

Other trials of Luspatercept

Trials testing the same drug.

Other Institute of Hematology & Blood Diseases Hospital, China trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05925504.

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