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Study of Bavituximab in Patients With Chronic Hepatitis C Virus Infection

Primary Purpose

Hepatitis C

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Bavituximab
Sponsored by
Peregrine Pharmaceuticals
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hepatitis C focused on measuring HCV, monoclonal antibody, phase 1

Eligibility Criteria

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

Inclusion Criteria: At least 18 years of age Chronic hepatitis C infection based on history and detectable serum HCV RNA Documented failure to respond to or relapse after treatment with pegylated interferon and ribavirin combination therapy Adequate hematologic function (absolute neutrophil count [ANC] greater than or equal to 1,500 cells/uL, hemoglobin [Hgb] greater than or equal to 12 g/dL in females and greater than or equal to 13 g/dL in males, platelet count greater than or equal to 100,000/uL and less than or equal to 500,000/uL) Adequate renal function (serum creatinine less than or equal to 1.5 mg/dL or calculated creatinine clearance greater than 60 mL/min) Normal coagulation profile (PT/INR and aPTT within institutional normal limits) D-dimer within institutional limits Female patients of childbearing potential must have a negative serum pregnancy test at prestudy and all patients of reproductive potential must be willing to use an approved form of barrier method contraception Exclusion Criteria: Prior exposure to any chimeric antibody Any other cause of liver disease other than chronic hepatitis C, such as autoimmune or alcoholic liver disease Decompensated clinical liver disease or cirrhosis Any evidence of clinically significant bleeding Known history of bleeding diathesis or coagulopathy Any history of thromboembolic events including central venous catheter-related thrombosis Any evidence or history of a hypercoagulable state (eg, elevated d-dimer or shortened aPTT) Concurrent therapy with oral or parenteral anticoagulants Concurrent hormone therapy (ie, estrogen contraceptives, hormone replacement, anti-estrogen) Antiviral therapy within 90 days of day 0 Investigational therapy within 4 weeks of day 0 Major surgery within 4 weeks of day 0 Uncontrolled intercurrent disease Any history of angina pectoris, coronary artery disease or cerebrovascular accident, or transient ischemic attack A history of any condition requiring anti-platelet therapy with the exception of general cardiovascular prophylaxis with aspirin A history of any condition requiring treatment (past or current) with coumarin-type agents Cardiac arrhythmia requiring medical therapy Serious non-healing wound Requirement for chronic daily treatment with NSAIDs, anti-platelet drugs (eg, phosphodiesterase inhibitors, adenosine diphosphate receptor antagonists), or steroids A disease or concurrent therapy known to cause significant alteration in immunologic function Known HIV or active hepatitis B virus (HBV) infection

Sites / Locations

  • Bach & Godofsky, MD, PA

Outcomes

Primary Outcome Measures

adverse events
laboratory evaluations
human anti-chimeric antibody
pharmacokinetic analysis
viral kinetic analysis

Secondary Outcome Measures

Full Information

First Posted
August 8, 2005
Last Updated
April 28, 2008
Sponsor
Peregrine Pharmaceuticals
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1. Study Identification

Unique Protocol Identification Number
NCT00128271
Brief Title
Study of Bavituximab in Patients With Chronic Hepatitis C Virus Infection
Official Title
A Phase 1 Study of Chimeric Anti-Phosphatidylserine Monoclonal Antibody (Bavituximab) in Patients Chronically Infected With Hepatitis C Virus (HCV) Who Are Non-Responders or Relapsers After Treatment With Pegylated Interferon Plus Ribavirin
Study Type
Interventional

2. Study Status

Record Verification Date
August 2006
Overall Recruitment Status
Completed
Study Start Date
August 2005 (undefined)
Primary Completion Date
August 2006 (Actual)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Peregrine Pharmaceuticals

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to determine the safety and tolerability of bavituximab when administered via a vein as a single infusion and to examine how bavituximab behaves in the body and how it affects the amount of hepatitis C virus in individuals with chronic infection.
Detailed Description
Hepatitis C virus (HCV) infection is a world wide public health concern and is the most common chronic bloodborne infection in the United States and the leading indication for liver transplantation. Laboratory and animal studies have demonstrated that bavituximab binds viruses and virally infected cells and prolongs survival in infected animals. This study will examine the safety and tolerability of bavituximab when administered to patients with chronic HCV infection who do not respond to or relapse after treatment with pegylated interferon plus ribavirin combination therapy. Groups of patients will be treated with escalating doses and followed for 12 weeks.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatitis C
Keywords
HCV, monoclonal antibody, phase 1

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
32 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Bavituximab
Primary Outcome Measure Information:
Title
adverse events
Title
laboratory evaluations
Title
human anti-chimeric antibody
Title
pharmacokinetic analysis
Title
viral kinetic analysis

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: At least 18 years of age Chronic hepatitis C infection based on history and detectable serum HCV RNA Documented failure to respond to or relapse after treatment with pegylated interferon and ribavirin combination therapy Adequate hematologic function (absolute neutrophil count [ANC] greater than or equal to 1,500 cells/uL, hemoglobin [Hgb] greater than or equal to 12 g/dL in females and greater than or equal to 13 g/dL in males, platelet count greater than or equal to 100,000/uL and less than or equal to 500,000/uL) Adequate renal function (serum creatinine less than or equal to 1.5 mg/dL or calculated creatinine clearance greater than 60 mL/min) Normal coagulation profile (PT/INR and aPTT within institutional normal limits) D-dimer within institutional limits Female patients of childbearing potential must have a negative serum pregnancy test at prestudy and all patients of reproductive potential must be willing to use an approved form of barrier method contraception Exclusion Criteria: Prior exposure to any chimeric antibody Any other cause of liver disease other than chronic hepatitis C, such as autoimmune or alcoholic liver disease Decompensated clinical liver disease or cirrhosis Any evidence of clinically significant bleeding Known history of bleeding diathesis or coagulopathy Any history of thromboembolic events including central venous catheter-related thrombosis Any evidence or history of a hypercoagulable state (eg, elevated d-dimer or shortened aPTT) Concurrent therapy with oral or parenteral anticoagulants Concurrent hormone therapy (ie, estrogen contraceptives, hormone replacement, anti-estrogen) Antiviral therapy within 90 days of day 0 Investigational therapy within 4 weeks of day 0 Major surgery within 4 weeks of day 0 Uncontrolled intercurrent disease Any history of angina pectoris, coronary artery disease or cerebrovascular accident, or transient ischemic attack A history of any condition requiring anti-platelet therapy with the exception of general cardiovascular prophylaxis with aspirin A history of any condition requiring treatment (past or current) with coumarin-type agents Cardiac arrhythmia requiring medical therapy Serious non-healing wound Requirement for chronic daily treatment with NSAIDs, anti-platelet drugs (eg, phosphodiesterase inhibitors, adenosine diphosphate receptor antagonists), or steroids A disease or concurrent therapy known to cause significant alteration in immunologic function Known HIV or active hepatitis B virus (HBV) infection
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eliot W Godofsky, MD, FACP
Organizational Affiliation
Bach & Godofsky, MD, PA
Official's Role
Principal Investigator
Facility Information:
Facility Name
Bach & Godofsky, MD, PA
City
Bradenton
State/Province
Florida
ZIP/Postal Code
34205
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Study of Bavituximab in Patients With Chronic Hepatitis C Virus Infection

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