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

Primary Purpose

Melanoma, Metastases

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
M200 (volociximab) in Combination with Dacarbazine (DTIC)
Sponsored by
PDL BioPharma, Inc.
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Melanoma focused on measuring Solid tumors, Metastatic melanoma

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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.

Sites / Locations

  • University of Alabama at Birmingham-Comprehensive Cancer Ctr.
  • Arizona Cancer Center
  • UCLA School of Medicine
  • Cancer Institute Medical Group, Inc.
  • University of Pittsburgh
  • Palmetto Hematology Oncology, P.C.
  • MD Anderson Cancer Center

Outcomes

Primary Outcome Measures

Proportion of patients with a confirmed tumor response at any time during the study.

Secondary Outcome Measures

Time to disease progression
Duration of tumor response
Pharmacokinetics (PK)
Immunogenicity

Full Information

First Posted
December 21, 2004
Last Updated
August 2, 2008
Sponsor
PDL BioPharma, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT00099970
Brief Title
Volociximab in Combination With DTIC in Patients With Metastatic Melanoma Not Previously Treated With Chemotherapy
Official Title
Phase II Open-Label Study of Volociximab in Combination With DTIC in Patients With Metastatic Melanoma Not Previously Treated With Chemo
Study Type
Interventional

2. Study Status

Record Verification Date
August 2008
Overall Recruitment Status
Completed
Study Start Date
December 2004 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
March 2006 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
PDL BioPharma, Inc.

4. Oversight

5. Study Description

Brief 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Melanoma, Metastases
Keywords
Solid tumors, Metastatic melanoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
40 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
M200 (volociximab) in Combination with Dacarbazine (DTIC)
Primary Outcome Measure Information:
Title
Proportion of patients with a confirmed tumor response at any time during the study.
Secondary Outcome Measure Information:
Title
Time to disease progression
Title
Duration of tumor response
Title
Pharmacokinetics (PK)
Title
Immunogenicity

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Steven J. O'Day, M.D.
Organizational Affiliation
Cancer Institute Medical Group, Inc.
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
John Kirkwood, M.D.
Organizational Affiliation
University of Pittsburgh
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Agop Y. Bedikian, MD
Organizational Affiliation
M.D. Anderson Cancer Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Antoni Ribas, MD
Organizational Affiliation
University of California, Los Angeles
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Colin P. Curran, M.D.
Organizational Affiliation
Palmetto Hematology Oncology, P.C.
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Andres Forero, M.D.
Organizational Affiliation
University of Alabama at Birmingham
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Lee Cranmer, M.D.
Organizational Affiliation
University of Arizona
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Alabama at Birmingham-Comprehensive Cancer Ctr.
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35294-3300
Country
United States
Facility Name
Arizona Cancer Center
City
Tucson
State/Province
Arizona
ZIP/Postal Code
85724
Country
United States
Facility Name
UCLA School of Medicine
City
Los Angeles
State/Province
California
ZIP/Postal Code
90095
Country
United States
Facility Name
Cancer Institute Medical Group, Inc.
City
Santa Monica
State/Province
California
ZIP/Postal Code
90404
Country
United States
Facility Name
University of Pittsburgh
City
Pittsburgh
State/Province
Pennsylvania
Country
United States
Facility Name
Palmetto Hematology Oncology, P.C.
City
Spartanburg
State/Province
South Carolina
ZIP/Postal Code
29303
Country
United States
Facility Name
MD Anderson Cancer Center
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States

12. IPD Sharing Statement

Learn more about this trial

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

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