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The purposes of this Phase 1/2 study are to examine the safety, tolerability, and antiviral activity of ISIS 14803, when given in combination with peginterferon alfa and ribavirin, to patients who either failed to have at least a 100-fold HCV reduction at Week 12 of standard therapy or still have detectable HCV at Week 24.
Previously untreated chronic hepatitis C patients undergoing therapy with peginterferon alfa and ribavirin have a very poor probability of achieving a sustained virologic response if they either do not have a 100-fold or greater reduction in their plasma HCV RNA levels at the 12th week of treatment or have detectable plasma HCV RNA at the 24th week of treatment. ISIS 14803 is an experimental antiviral medication for the treatment of chronic hepatitis C that has been given to chronic hepatitis C patients in two previous single-agent clinical trials (approximately 70 patients). In this clinical research study, 12 weeks of ISIS 14803 treatment will be added to the peginterferon alfa and ribavirin treatment regimen of previously untreated chronic hepatitis C patients who have a very poor probability of achieving a sustained virologic response based upon either of the above two criteria. Enrolled patients must continue to be treated with peginterferon alfa and ribavirin and must begin ISIS 14803 treatment within four weeks of their HCV RNA result report date. ISIS 14803 will be given as a two-hour intravenous infusion, two times each week, for 12 weeks. Depending on their HCV response to the three-drug combination, patients may continue treatment with peginterferon alfa and ribavirin after the end of ISIS 14803 treatment. Patients will be monitored for at least eight weeks (for safety) after the end of ISIS 14803 treatment and possibly for longer (for sustained virologic response). Two dose levels of ISIS 14803 will be studied in this trial, 3 and 6 mg/kg ideal body weight.
Age
18 - 65 years
Sex
ALL
Healthy Volunteers
No
Birmingham Gastroenterology Associates
Birmingham, Alabama, United States
Mayo Clinic Hospital
Phoenix, Arizona, United States
Community Clinical Trials
Orange, California, United States
The Lynn Institute of the Rockies
Colorado Springs, Colorado, United States
Western States Clinical Research, Inc.
Wheat Ridge, Colorado, United States
University of Florida
Jacksonville, Florida, United States
Miami Research Associates, Inc.
Miami, Florida, United States
Idaho Gastroenterology Assoc.
Boise, Idaho, United States
IMG Healthcare, LLC
New Orleans, Louisiana, United States
Beth Israel Deconess Medical Center
Boston, Massachusetts, United States
Start Date
June 1, 2003
Primary Completion Date
January 1, 2004
Completion Date
January 1, 2004
Last Updated
December 5, 2022
22
Estimated participants
ISIS 14803, peginterferon alfa, ribavirin
DRUG
Lead Sponsor
Ionis Pharmaceuticals, Inc.
NCT05870969
NCT03987503
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT04382404