Repeat-Dose Study of Bavituximab in Patients With Chronic Hepatitis C
NCT00343525 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 24
Last updated 2008-05-07
Summary
The purpose of this study is to determine the safety and tolerability of bavituximab when administered via an arm vein as multiple infusions and to examine how bavituximab behaves in the body and how it effects the amount of hepatitis C virus and immune modulators in individuals with chronic infection.
Conditions
- Hepatitis C
Interventions
- DRUG
-
bavituximab
Sponsors & Collaborators
-
Peregrine Pharmaceuticals
lead INDUSTRY
Principal Investigators
-
Eric Lawitz, MD · Alamo Medical Research
-
Eliot W Godofsky, MD · University Hepatitis Center
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2006-05-31
- Primary Completion
- 2007-01-31
Countries
- United States
Study Locations
More Related Trials
-
A Study to Evaluate Chronic Hepatitis C Infection in Treatment Experienced Adults
NCT01715415 ·Status: COMPLETED ·Phase: PHASE3
-
A Study to Evaluate Chronic Hepatitis C Infection in Adults With Genotype 1b Infection
NCT01767116 ·Status: COMPLETED ·Phase: PHASE3
-
A Study to Evaluate Chronic Hepatitis C Infection
NCT01716585 ·Status: COMPLETED ·Phase: PHASE3
-
A Study to Evaluate Chronic Hepatitis C Infection in Adults With Genotype 1a Infection
NCT01833533 ·Status: COMPLETED ·Phase: PHASE3
-
A Follow up Study Designed to Obtain Long Term Data on Participants Who Either Achieved a Sustained Virologic Response or Did Not Achieve a Sustained Virologic Response in an AbbVie Sponsored Hepatitis C Study
NCT01773070 ·Status: COMPLETED ·Phase: PHASE3
-
Safety, Antiviral Activity and PK of MRD of BI 201335 in Chronic Hepatitis C Patients Both Treatment Naive and -Experienced
NCT00793793 ·Status: COMPLETED ·Phase: PHASE1
-
Study of XTL6865 in Patients With Chronic Hepatitis C Virus Infection
NCT00300807 ·Status: UNKNOWN ·Phase: PHASE1
-
A Study to Evaluate Long-term Outcomes Following Treatment With ABT-450/Ritonavir/ABT-267 (ABT-450/r/ABT-267) and ABT-333 With or Without Ribavirin (RBV) in Adults With Genotype 1 Chronic Hepatitis C Virus (HCV) Infection
NCT02167945 ·Status: COMPLETED ·Phase: PHASE3
-
Study of Viramidine to Ribavirin in Patients With Chronic Hepatitis C Who Are Treatment Naive
NCT00093093 ·Status: COMPLETED ·Phase: PHASE3
-
Proof-of-concept Study to Evaluate the Safety and Immunomodulatory Effects of SCV 07 as Monotherapy or in Combination With Ribavirin in Noncirrhotic Subjects With Chronic Hepatitis C Who Have Relapsed
NCT00968357 ·Status: COMPLETED ·Phase: PHASE2
-
A Study of Ombitasvir/Paritaprevir/Ritonavir and Dasabuvir With or Without Sofosbuvir and Ribavirin in Direct-Acting Antiviral Agent Treatment-Experienced Adults With Chronic Hepatitis C Virus Infection
NCT02356562 ·Status: COMPLETED ·Phase: PHASE2
-
Ombitasvir/ABT-450 (Paritaprevir)/Ritonavir With Dasabuvir and Ribavirin (RBV) in Treatment Naive and Treatment Experienced Genotype 1a Hepatitis C Virus Infected Adults
NCT02476617 ·Status: COMPLETED ·Phase: PHASE3
-
3-year Follow-up Study in Patients Previously Treated With TMC435-Containing Regimen for the Treatment of Hepatitis C Virus Infection
NCT01349465 ·Status: COMPLETED ·Phase: PHASE3
-
Study of Viramidine to Ribavirin in Patients With Chronic Hepatitis C Who Are Treatment-Naive
NCT00230958 ·Status: COMPLETED ·Phase: PHASE3
-
Multiple Ascending Dose Study of Miravirsen in Treatment-Naïve Chronic Hepatitis C Subjects
NCT01200420 ·Status: COMPLETED ·Phase: PHASE2
-
Safety, Antiviral Effect and PK of BI 207127 + BI 201335 +/- RBV for 4 up to 40 Weeks in Patients With Chronic HCV Genotype 1 Infection
NCT01132313 ·Status: COMPLETED ·Phase: PHASE2
-
Study to Assess the Safety, Tolerability, Pharmacokinetics and Antiviral Activity of ABT-267 in HCV Infected Subjects
NCT01563536 ·Status: COMPLETED ·Phase: PHASE2
-
Viral Kinetics and Liver Gene Expression in Response to Ribavirin and Peginterferon Therapy of Chronic Hepatitis C
NCT00718172 ·Status: COMPLETED ·Phase: PHASE1
-
Comparison of Two Triple Regimens for Treatment and Retreatment of Chronic Hepatitis C Infection
NCT01771653 ·Status: COMPLETED
-
Ombitasvir/Paritaprevir/Ritonavir and Dasabuvir With and Without Ribavirin in Protease-Inhibitors ("PI") Failures
NCT02646111 ·Status: UNKNOWN ·Phase: PHASE3
-
DAA Based Therapy for Recently Acquired Hepatitis C (DARE-C)
NCT01743521 ·Status: COMPLETED ·Phase: PHASE4
-
S-Adenosyl Methionine (SAMe) to Treat Patients With Chronic Hepatitis C
NCT00475176 ·Status: COMPLETED ·Phase: PHASE2
-
Direct-acting Antiviral Therapy and Reinfection Among PWID With Chronic HCV in Community-based Settings
NCT03343925 ·Status: COMPLETED
-
A Phase 1b, Single Center, Clinical Study to Investigate the Safety and Biological Responses to Baminercept in Patients With Chronic HCV Hepatitis.
NCT01164384 ·Status: UNKNOWN ·Phase: PHASE1
-
Boceprevir/Peginterferon/Ribavirin for Chronic Hepatitis C: Erythropoietin Use Versus Ribavirin Dose Reduction for Anemia (P06086 AM2)
NCT01023035 ·Status: COMPLETED ·Phase: PHASE3