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Multi-center, Survival Data Collection in Subjects Previously Enrolled in Celgene Protocol CC-5013-MDS-003

18 Years
Not Enrolling
Myelodysplastic Syndrome

Thank you

Trial Information

Multi-center, Survival Data Collection in Subjects Previously Enrolled in Celgene Protocol CC-5013-MDS-003

Inclusion Criteria:

1. Must have been enrolled in the Celgene protocol CC-5013-MDS-003 study.

2. Must understand and be able to give informed consent (if a subject is deceased,
proper legal consent (i.e. next of kin, legal representative) will be obtained prior
to collection of data).

Exclusion Criteria:

1. Consent refused for any reason at current or long-term follow up completed in 2007
(long-term follow up: survival data collection completed to obtain further safety
information on CC-5013-MDS-003 discontinued subjects from May - October 2007).

Type of Study:


Study Design:

Time Perspective: Retrospective

Outcome Measure:

Participants Survival Status as of the Time of the Extension Study Follow-up

Outcome Description:

Count of participants who were alive or deceased at the time of the extension study follow-up.

Outcome Time Frame:

up to 7 years

Safety Issue:


Principal Investigator

Barry Skikne, MD

Investigator Role:

Study Director

Investigator Affiliation:

Celgene Corporation


United States: Institutional Review Board

Study ID:




Start Date:

March 2010

Completion Date:

October 2010

Related Keywords:

  • Myelodysplastic Syndrome
  • MDS
  • Myelodysplastic Syndromes
  • Preleukemia



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