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NCT07008820

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

Recruiting now Last updated 4 December 2025
What this trial tests

trial testing Health-related quality of life questionnaires in Myelodysplastic Syndrome (MDS) in 50 participants. Currently enrolling.

Timeline
13 May 2025
Primary endpoint
28 February 2026
28 February 2026

Quick facts

Lead sponsorBristol-Myers Squibb
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment50
Start date13 May 2025
Primary completion28 February 2026
Estimated completion28 February 2026
Sites1 location across Japan

Drugs / interventions tested

Conditions studied

Sponsor

Bristol-Myers Squibb — full company profile →

Who can join

Adults 18 to 80, any sex, with Myelodysplastic Syndrome (MDS). Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study will examine quality of life, experiences, and unmet needs among individuals diagnosed with Low Risk Myelodysplastic Syndrome who are erythropoietin stimulating agent naïve and non-transfusion dependent and among individuals with suspected myelodysplastic syndromes with unexplained anemia in Japan

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Myelodysplastic Syndrome (MDS)

Currently open trials in the same condition.

Other Bristol-Myers Squibb trials

Trials by the same sponsor.

Verify against primary sources

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/NCT07008820.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing