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Asia Myelodysplastic Syndrome (MDS) Registry

Bristol-Myers Squibb (BMS) logo

Bristol-Myers Squibb (BMS)

Status

Not yet enrolling

Conditions

Myelodysplastic Syndromes (MDS)

Treatments

Drug: Prescribed treatments for myelodysplastic syndromes (MDS)

Study type

Observational

Funder types

Industry

Identifiers

NCT07355478
CA056-1131

Details and patient eligibility

About

The purpose of this study is to provide a contemporary view and offer invaluable insights into the demographic profiles, clinical characteristics, treatments, and real-world outcomes of individuals with myelodysplastic syndromes (MDS) in Asia.

Enrollment

500 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Retrospective enrolment of Myelodysplastic Syndrome (MDS) participants:

  • Aged at least 18 years at initial diagnosis of MDS
  • Diagnosed with MDS according to World Health Organization (WHO) 2008, WHO 2016, or WHO 2022 criteria between 1 January 2019 and 31 December 2022; and
  • Diagnosed with MDS within 100 days from the date of diagnostic bone marrow (BM) aspirate

Inclusion criteria for the prospective enrolment of MDS participants:

  • Aged at least 18 years at initial diagnosis of MDS; and
  • Diagnosed with MDS according to World Health Organization (WHO) 2008, WHO 2016, or WHO 2022 criteria between 1 October 2025 and 30 September 2026; and
  • Diagnosed with MDS within 100 days from the date of diagnostic BM aspirate

Exclusion criteria

• None

Trial design

500 participants in 1 patient group

Group 1
Description:
Participants diagnosed with myelodysplastic syndromes (MDS)
Treatment:
Drug: Prescribed treatments for myelodysplastic syndromes (MDS)

Trial contacts and locations

2

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Central trial contact

First line of the email MUST contain NCT # and Site #.; BMS Study Connect Contact Center www.BMSStudyConnect.com

Data sourced from clinicaltrials.gov

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