Multiple Myeloma Clinical Trial

Clinical Trial Finder Multiple Myeloma Trials

A Phase II Study of Continuous Versus Syncopated Dosing of CC-5013 for the Treatment of Refractory Multiple Myeloma

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Summary

To evaluate the response rate, response duration, and survival of patients treated with CC-5013 in a chronic dosing schedule versus a syncopated dosing schedule.

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Eligibility Criteria

History of histologically documented multiple myeloma with relapsed or resistant disease
Pregnant or nursing women may not participate. Women of childbearing potential must have a negative pregnancy documented within one week of registration. Women of reproductive potential may not participate unless they have agreed to use an effective contraceptive method.
Signed written informed consent and willingness to meet follow-up schedule and study procedure obligations

Study is for people with:

Multiple Myeloma

Phase:

Phase 2

Estimated Enrollment:

100

Study ID:

NCT00051116

Recruitment Status:

Completed

Sponsor:

Celgene Corporation

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There is 1 Location for this study

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Myeloma Institute University of Arkansas for Medical Sciences
Little Rock Arkansas, 72205, United States

How clear is this clinincal trial information?

Study is for people with:

Multiple Myeloma

Phase:

Phase 2

Estimated Enrollment:

100

Study ID:

NCT00051116

Recruitment Status:

Completed

Sponsor:


Celgene Corporation

How clear is this clinincal trial information?

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