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Patient Reported Outcomes and Patient Voice Among Patients Diagnosed With Low Risk Myelodysplastic Syndrome (LR-MDS) or Unexplained Anemia In Japan

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NCT07008820

Sponsored by Bristol-Myers Squibb (industry) · BMY — their whole pipeline →.

Phase
Status
Completed
Study type
Observational
Enrollment
56actual
Sites
1
Country
Japan

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2025-05-13actualWhen the study began enrolling
Primary completion2026-02-24actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-02-24actualThe whole study's end, after follow-up
First posted2025-06-06actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-05-26actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Myelodysplastic Syndrome (MDS)

Interventions

  • Other: Health-related quality of life questionnaires
  • Other: Qualitative interviews

Primary outcomes

what the primary-completion date above is the date OF
Participant quality of life as assessed by the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC-QLQ C30) patient reported outcome questionnaire
measured Day 1
Participant anemia symptoms as assessed by the Functional Assessment of Cancer Therapy - Anemia (FACT-An) patient reported outcome questionnaire
measured Day 1
Symptom severity as assessed by the Patient Global Impression-Severity (PGI-S) patient reported outcome questionnaire
measured Day 1
General health status of participants as assessed by the EQ-5D-5L patient reported outcome questionnaire
measured Day 1
Participant baseline socio-demographics
measured Baseline
Participant baseline clinical characteristics
measured Baseline

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