Melanoma Clinical Trial

Volociximab in Combination With DTIC in Patients With Metastatic Melanoma Not Previously Treated With Chemotherapy

Summary

This clinical trial is being conducted to determine tumor response and preliminary safety of a monoclonal antibody that specifically binds to a cell surface receptor (α5β1 integrin) that is required for the establishment of new blood vessels during tumor growth, a process known as angiogenesis.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Males and females of at least 18 years of age with stage IV or unresectable stage III non-ocular melanoma who may have received 0 to 2 prior regimens for metastatic disease with a biological therapy or immunotherapy (e.g., IL-2 or interferon-alfa).
Measurable disease according to Response Criteria for Solid Tumors (RECIST).
Eastern Cooperative Oncology Group (ECOG) performance status less than or equal to 1.
Estimated survival is greater or equal to 4 months.
Negative pregnancy test (women of childbearing potential only).
Pretreatment laboratory levels that meet specific criteria.
Signed informed consent, including permission to use protected health information.

Exclusion Criteria:

Prior treatment with M200 or a5b1 inhibitors and murine or chimeric monoclonal antibodies.
Prior treatment with DTIC, temozolomide, or other chemotherapeutic regimens.
Known sensitivity to murine proteins or chimeric antibodies or other components of the product.
Use of any investigational drug within 4 weeks prior to screening or 5 half-lives of the prior investigational drug (whichever is longer).
Systemic biologic, immunotherapy, and/or radiation therapy within 4 weeks of the first dose of M200.
Documented central nervous system (CNS) tumor or CNS metastasis.
History of thromboembolic events and bleeding disorders within the past year.
Medical conditions that may be exacerbated by bleeding.

Study is for people with:

Melanoma

Phase:

Phase 2

Estimated Enrollment:

40

Study ID:

NCT00099970

Recruitment Status:

Completed

Sponsor:

PDL BioPharma, Inc.

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There are 6 Locations for this study

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University of Alabama at Birmingham-Comprehensive Cancer Ctr.
Birmingham Alabama, 35294, United States
Arizona Cancer Center
Tucson Arizona, 85724, United States
UCLA School of Medicine
Los Angeles California, 90095, United States
Cancer Institute Medical Group, Inc.
Santa Monica California, 90404, United States
University of Pittsburgh
Pittsburgh Pennsylvania, , United States
Palmetto Hematology Oncology, P.C.
Spartanburg South Carolina, 29303, United States
MD Anderson Cancer Center
Houston Texas, 77030, United States

How clear is this clinincal trial information?

Study is for people with:

Melanoma

Phase:

Phase 2

Estimated Enrollment:

40

Study ID:

NCT00099970

Recruitment Status:

Completed

Sponsor:


PDL BioPharma, Inc.

How clear is this clinincal trial information?

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