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NCT06045689 · ClinicalTrials.gov registry record · Phase 3
A Study to Assess Luspatercept in Lower-risk Myelodysplastic Syndrome Participants
A Phase 3 study of Myelodysplastic Syndromes, sponsored by Bristol-Myers Squibb.
- Active
- Registry status
- Phase 3
- Development phase
- 106
- Enrollment target
- 20
- Study locations
NCT06045689 is a Phase 3 study of Myelodysplastic Syndromes that is active but no longer recruiting, run by Bristol-Myers Squibb. The registered enrollment target is 106 participants, below the 284-participant average among 173 other Myelodysplastic Syndromes trials with a reported enrollment target (63% lower). The trial reports 20 study locations across 17 states.
The verdict
NCT06045689, a Phase 3 study of Myelodysplastic Syndromes, is active but no longer recruiting, sponsored by Bristol-Myers Squibb.
- ACTIVE NOT RECRUITING
- Registry status
- Phase 3
- Development phase
- 106 participants
- Enrollment target
- 20
- Study locations
Study Summary
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.
Conditions Studied
Interventions
- DRUG Luspatercept
Study Locations (20)
Florida
- Local Institution - 0055 - St. Petersburg
- Local Institution - 0056 - Wellington
Texas
- Local Institution - 0043 - Amarillo
- Local Institution - 0022 - Huntsville
Praha, Hlavní Mesto
- Local Institution - 0023 - Prague
- Local Institution - 0004 - Prague
California
- Local Institution - 0051 - Los Alamitos
Connecticut
- Local Institution - 0033 - New Haven
Kansas
- Local Institution - 0020 - Kansas City
Kentucky
- Local Institution - 0025 - Paducah
Michigan
- Local Institution - 0011 - Detroit
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 106 participants |
| Start Date | 2023-10-05 |
| Est. Completion | 2027-12-30 |
| Phase | Phase 3 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06045689
The ClinicalTrials.gov registry entry for NCT06045689 describes a study currently listed as active not recruiting, categorized as Phase 3. The registered enrollment target is 106 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 284-participant average among 173 other Myelodysplastic Syndromes trials with a reported enrollment target (63% lower). The listed sponsor is Bristol-Myers Squibb, which has 1,025 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Myelodysplastic Syndromes appearing as the primary indexed condition, and to 1 intervention - of which Luspatercept is the first listed.
NCT06045689 reports 20 study locations spanning 17 distinct geographic areas - top geographies include Florida, Texas, Praha, Hlavní Mesto.
Frequently Asked Questions
What is clinical trial NCT06045689 about?
NCT06045689 is a clinical study titled "A Study to Assess Luspatercept in Lower-risk Myelodysplastic Syndrome Participants". 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.
What is the current status of trial NCT06045689?
This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 106 participants. The study started on 2023-10-05. Estimated completion is 2027-12-30.
What conditions does trial NCT06045689 study?
This clinical trial studies the following conditions: Myelodysplastic Syndromes.
What interventions are being tested in trial NCT06045689?
The interventions under investigation include: Luspatercept (DRUG).
Who is sponsoring clinical trial NCT06045689?
This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06045689 being conducted?
This trial has 20 study locations across California, Connecticut, Florida, Kansas, Kentucky. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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