Multiple Myeloma Clinical Trial

Study of SGN-40, Lenalidomide, and Dexamethasone in Patients With Multiple Myeloma

Summary

This is a Phase I, open-label, multi-dose trial to define the MTD and tolerability of a regimen including lenalidomide, dexamethasone, and intravenous SGN-40 in patients with relapsed multiple myeloma.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Diagnosis of multiple myeloma.
Received at least one prior systemic therapy other than single-agent corticosteroids.
Measurable disease of monoclonal protein greater than or equal to 0.5 gram/dL in plasma or 0.5 gram/24 hr urine collection, or greater than 10 mg/dL free light chain (FLC) in serum as determined by serum FLC assay and provided the serum FLC ratio is abnormal.

Exclusion Criteria:

Received an allogenic stem cell transplant.
Previous intolerance of lenalidomide or dexamethasone.
Primary invasive malignancy (other than multiple myeloma) within the last 3 years.

Study is for people with:

Multiple Myeloma

Phase:

Phase 1

Estimated Enrollment:

36

Study ID:

NCT00525447

Recruitment Status:

Completed

Sponsor:

Seagen Inc.

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There are 9 Locations for this study

See Locations Near You

Rocky Mountain Cancer Center
Denver Colorado, 80218, United States
H. Lee Moffitt Cancer Center & Research Institute
Tampa Florida, 33612, United States
Dana Farber Cancer Institute
Boston Massachusetts, 02115, United States
Barbara Ann Karmanos Cancer Institute
Detroit Michigan, 48201, United States
Nebraska Methodist Hospital
Omaha Nebraska, 68114, United States
Hackensack University Medical Center
Hackensack New Jersey, 07601, United States
Weill Medical College of Cornell University
New York New York, 10021, United States
Avera Cancer Institute
Sioux Falls South Dakota, 57105, United States
Baylor University Medical Center
Dallas Texas, 75246, United States

How clear is this clinincal trial information?

Study is for people with:

Multiple Myeloma

Phase:

Phase 1

Estimated Enrollment:

36

Study ID:

NCT00525447

Recruitment Status:

Completed

Sponsor:


Seagen Inc.

How clear is this clinincal trial information?

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