NCT Number: NCT00099970
Volociximab in Combination With DTIC in Patients With Metastatic Melanoma Not Previously Treated With Chemotherapy
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.
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Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 2
Primary location
University of Alabama at Birmingham-Comprehensive Cancer Ctr., Birmingham, Alabama, United States
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
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.
Treatment and study plan
Primary outcomes
-
Proportion of patients with a confirmed tumor response at any time during the study.
Secondary outcomes
-
Time to disease progression
-
Duration of tumor response
-
Pharmacokinetics (PK)
-
Immunogenicity
Sponsors and collaborators
Lead sponsor
PDL BioPharma, Inc.
Industry
Registry information
Official study title
Phase II Open-Label Study of Volociximab in Combination With DTIC in Patients With Metastatic Melanoma Not Previously Treated With Chemo
Important dates
- Study start
- 2004
- Study completion
- 2006
- First posted
- Dec 22, 2004
- Registry last updated
- Aug 5, 2008
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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