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Spots Global Cancer Trial Database for Study of the Safety and Efficacy of CC-5013 Treatment For Patients With Myelodysplastic Syndrome

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Study of the Safety and Efficacy of CC-5013 Treatment For Patients With Myelodysplastic Syndrome

Official Title: A Phase II Open Label Study of the Safety and Efficacy of CC-5013 Treatment For Patients With Myelodysplastic Syndrome

Study ID: NCT00044382

Interventions

CC-5013

Study Description

Brief Summary: To estimate the percent of patients with myelodysplastic syndromes (MDS) who experience erythroid response and the interval to response with daily treatment of 25 mg of CC-5013 .

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Arizona Cancer Center, Tucson, Arizona, United States

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

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