Peginterferon Alpha-2a and Ribavirin to Treat Hepatitis C in HIV-infected Patients (PIFNPK)
National Institute of Allergy and Infectious Diseases (NIAID)
Information provided by (Responsible Party)
National Institutes of Health Clinical Center (CC)
First received: June 16, 2004
Last updated: June 21, 2011
Last Verified: June 2011
History of Changes
This study will evaluate the safety and effectiveness of combination therapy with
peginterferon alpha-2a and ribavirin for treating hepatitis C virus (HCV) infection in
HIV-infected patients. Peginterferon alpha with ribavirin is the therapy of choice for people
with HCV alone. Peginterferon alpha-2a is a compound that results from attaching a
polyethylene glycol molecule to interferon alpha-2a. This compound stays in the blood longer
than unmodified interferon alpha-2a, causing a higher blood concentration and thus
maintaining greater activity against the hepatitis C virus.
HIV-infected patients 18 years of age and older with chronic hepatitis C infection and a viral load greater than 2000 copies/mL may be eligible for this 2-1/2 year study. Candidates are screened with a medical history and physical examination, blood and urine tests, eye examination, chest x-ray, electrocardiogram (EKG), liver ultrasound, and pregnancy test in women who are able to become pregnant. If a recent liver biopsy is not available, this test is done to determine the type and severity of liver disease. The patient is given a sedative before the procedure. Then, the skin in the area over the biopsy site is numbed with a local anesthetic and a needle is inserted rapidly into and out of the liver to obtain a small tissue sample. The patient remains in the hospital overnight for monitoring.
Participants begin treatment with injections under the skin of peginterferon alpha-2a and ribavirin pills by mouth on study day 0. Peginterferon is given either once or twice a week for 4 weeks and then once a week for 44 weeks. Ribavirin is given daily. In addition, patients continue to take all other medications prescribed by their doctor. Clinic visits are scheduled for the following procedures:
- Days 1, 3, 4, 7, 10 and weeks 2, 3, and 4 - Blood tests for safety measures and to measure blood levels of HIV and HCV.
- Weeks 6, 8, 12, 16, 20, 24, 28, 32, 36, 40, 44 - Blood and urine tests to determine the side effects of treatment and its effect on the HCV infection. In addition, eye examinations are done every 3 months, and pregnancy and thyroid function tests are done several times during the treatment period.
- Week 48 or end of treatment - Treatment stops after 48 weeks. At this time, or earlier for those who do not complete the 48 weeks, patients return to the clinic for a chest x-ray, EKG, blood tests, and abdominal ultrasound. Patients are hospitalized for a repeat liver biopsy.
- Weeks 52, 56, 64 and 72 - Blood and urine tests to determine the side effects of
Drug : Double dose pegylated interferon with weight based Ribavirin
Drug : standard dose pegylated interferon alfa -2a and ribavirin
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
|Official Title:||A Randomized Controlled Trial to Evaluate the Safety and Efficacy of Twice-Weekly Peginterferon Alpha 2a and Ribavirin Induction Therapy for Chronic Hepatitis C in Patients Who Are Coinfected With HIV-1|
Further study details as provided by National Institutes of Health Clinical Center (CC):
Primary Outcome Measures
Number of Participants With Sustained Virologic Response (SVR)
[ Time Frame: 72 weeks ]
SVR [ Sustained virological response] SVR was defined as HCV RNA levels below the limit of detection 24 weeks after the end of treatment.
- Number of Participants With Normalization of Liver Enzymes
[ Time Frame: week 24, week 48, week 72 ]
normalization of liver enzymes :Alanine aminotransferase (ALT) and Aspartate aminotransferase (AST) Alanine aminotransferase (ALT): Normal 6 - 41 U/L Aspartate aminotransferase (AST) : Normal 9 - 34 U/L
- Number of Participants With Adverse Events
[ Time Frame: 48 weeks ]
Adverse Events - Anemia, Neutropenia and Psychiatric adverse events
|Study Start Date:||June 2004|
|Study Completion Date:||November 2008|
|Primary Completion Date:||November 2008 (Final data collection date for primary outcome measure)|
Standard dose arm
Pegylated interferon alfa -2a STANDARD DOSE Pegasys 180ug/week
standard dose pegylated interferon alfa -2a and ribavirin
pegylated interferon alfa -2a 180ug weekly and weight based ribavirin for duration of the treatment
Other Name: pegasys
Double dose arm
Double dose pegylated interferon with weight based Ribavirin
Double dose pegylated interferon with weight based Ribavirin
pegylated interferon alfa -2a 180ug/twice weekly and weight based ribavirin for 4 weeks then pegylated interferon alfa -2a 180ug/ weekly for the remainder of the treatment
Other Name: Pegasys
Hepatitis C infection occurs in one-third of all HIV-infected individuals. Liver disease has become more significant among patients coinfected with HIV and HCV. Several studies have shown that coinfected individuals develop earlier and more severe liver disease. Pegylated interferon alpha with ribavirin has become the therapy of choice among people with HCV alone. This is a randomized controlled study to address the safety and efficacy of a 4 week induction therapy consisting of twice-weekly pegylated interferon alpha-2a and daily ribavirin on HIV-1 and hepatitis C coinfected individuals. Twenty-two patients who are infected with both HIV and HCV and who also have evidence of chronic hepatitis will be randomized to receive peginterferon alpha-2a either twice weekly or once weekly for four weeks. They will then continue with standard weekly peginterferon for 44 more weeks. The patients will receive standard daily dose of ribavirin during the entire 48 weeks. These patients will be monitored for peginterferon level, HCV viral load, HIV viral load and CD4 counts and undergo a baseline liver biopsy and another at the end of 72 weeks. The results of the study will enable us to better delineate the efficacy of twice weekly peginterferon induction therapy in suppressing the hepatitis C virus in the first 4 weeks of the therapy. Since viral suppression for hepatitis C in the early phase of the combination treatment has predictive values for long term eradication of the virus, a therapy that improves early viral suppression may improve the long term cure rate. This will be especially important given the current low cure rate of HCV among HIV coinfected individuals.Eligibility
|Ages Eligible for Study:||18 Years and older|
|Sexes Eligible for Study:||All|
|Accepts Healthy Volunteers:||No|
- Age greater than or equal to18 years.
- Documentation of HIV-1 infection by licensed ELISA test and confirmed by a Western Blot.
- Documentation of Hepatitis C infection by demonstration of a positive test for hepatitis C antibody and on HCV RNA level of 2000 or greater.
- Histopathologic features consistent with chronic hepatitis C on liver biopsy at the time of enrollment. A liver biopsy done for a subject within a year prior to his or her participation may be used as the baseline biopsy.
- Patients with CD4+ cell count greater than 200 cells/mm3 or CD4+ cell percentage greater than 14%.
- Ability to sign informed consent and willingness to comply with the study requirements and clinic policies.
- Serum phosphorus greater than or equal to 2.2 mg/dL and less than or equal to 4.4 (normal range NIH 2.3-4.3 mg/dL).
- Neutrophil count greater than or equal to 1000 cells/mm3.
- Platelets greater than or equal to 50,000/ mm3.
- Hemoglobin greater than or equal to 10.5 mg/dL.
- ALT less than 7 X the NIH upper limit of normal.
- Serum lipase less than 1.5 X the NIH upper limit of normal.
- Not pregnant or breast-feeding. Pregnancy test must be negative within two weeks prior to dosing with study medications.
- If the patient is able to become pregnant then she must use two effective methods of contraception during the study. Effective contraceptive methods include abstinence, surgical sterilization of either partner, barrier methods such as diaphragm, condom, cap or sponge, or use of hormonal contraception with an anti-HIV regimen that will not alter metabolism of hormonal contraception. This is advised on the basis of using ribavirin, which may have a potential teratogenic effect in pregnant women.
- Need to have a primary doctor outside of OP8 or as part of the OP8 training clinic who will be taking care of the patients for their HIV infection and liver disease.
- Willing to designate a person for durable power of attorney on the NIH form for medical research and medical care purposes at the NIH Clinical Center.
- Able to learn to safely inject medication subcutaneously or be able to find another person or a clinic to inject for him/her.
- Patient should not be on other experimental therapies during their participation in this protocol.
- Patients should not have used interferon or peginterferon previously for the treatment of hepatitis C
- Liver histology which, in the opinion of Clinical center pathologist, is consistent with any other co-existent cause of chronic liver disease as defined as chronic hepatitis B with positive HBSag, autoimmune hepatitis with a positive ANA greater than 1 unit or positive anti mitochondrial antibody greater than 1 unit, cholestatic disease with persistent elevation of Alkaline phosphatase, primary biliary cirrhosis or sclerosing cholangitis, Wilson's disease, alpha-1-antitrypsin deficiency, steatohepatitis (alcohol or non alcoholic) with marked steatosis, many Mallory bodies, or extensive zone 3 periportal fibrosis.
- Hemochromatosis or secondary iron overload as defined by (1) an elevated serum ferritin or an iron saturation (serum iron/IBC X 100%) of greater than 50% and (2) presence of 3+ or more stainable Iron on liver biopsy according to the study pathologist or a history of previous phlebotomy for Iron overload will undergo HFE genetic counseling and those with a positive HFE genetic test demonstrating homozygosity for C282Y and H63D are not eligible. Those who have compound heterozygosity to C282Y and H63D are also not eligible.
- Child Turcotte Pugh score greater than 7.
- PT-INR greater than 2 or history of hemophilia.
- Organ transplant recipient.
- Creatinine clearance less than 50 mL/min.
- Elevated alpha-fetoprotein level (greater than 100 ng/mL).
- Coexisting neoplastic disease except for Kaposi's Sarcoma, any non-metastatic skin cancer that has been resected, non-metastatic cervical or anal cancer that has been resected.
- Severe cardiac or pulmonary decompensation.
- Severe psychiatric disorder that would interfere with the adherence to protocol requirements.
- Preexisting autoimmune disorders including inflammatory bowel diseases, psoriasis, and optic neuritis.
- Preexisting uncontrolled seizure disorder.
- Preexisting pancreatitis.
- Severe retinopathy as determined by the ophthalmologist.
- Currently taking didanosine as part of antiretroviral regimen.
- Direct bilirubin greater than 0.6 mg/dL.
- Using long-term systemic corticosteroids, immunosuppressives, or cytotoxic agents within 60 days of enrollment into the trial.
- Chronic viral hepatitis of any other etiology other than hepatitis C.
- Active systemic infections other than hepatitis C and HIV.
- Liver disease caused by reasons other than hepatitis C like HBV, HDV, Wilson's, hemochromatosis, autoimmune hepatitis (ANA greater than 1 unit) except history of drug-associated hepatitis with discontinuation of the causative agent.
- Hepatic mass suggestive of hepatocellular carcinoma as detected by ultrasound scan.
- Alcohol or substance abuse that potentially could interfere with patient compliance.
- History of esophageal varices.
- Any systemic illness that will make it unlikely that the subject will be able to return to NIH for the required study visits.
- Evidence of gastrointestinal malabsorption or chronic nausea or vomiting.
- Male partners of pregnant women.
- Pregnant women.
- Breastfeeding women.
Contacts and LocationsChoosing to participate in a study is an important personal decision.Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below.For general information, see Learn About Clinical Studies.
Please refer to this study by its ClinicalTrials.gov identifier: NCT00085917
Locations Show More
|United States, Maryland|
|National Institutes of Health Clinical Center, 9000 Rockville Pike|
|Bethesda, Maryland, United States, 20892|
Sponsors and CollaboratorsNational Institute of Allergy and Infectious Diseases (NIAID)
|Principal Investigator:||Shyam Kottilil||National Institute of Allergy and Infectious Diseases (NIAID)|
|Responsible Party:||Shyamasundaran Kottilil, M.D./National Institute of Allergy and Infectious Diseases, National Institutes of Health|
|ClinicalTrials.gov Identifier:||NCT00085917 History of Changes|
|Other Study ID Numbers:||040187|
|Study First Received:||June 16, 2004|
|Last Updated:||June 21, 2011|
Keywords provided by National Institutes of Health Clinical Center (CC):Pegasys
Early Virological Response
Additional relevant MeSH terms:
ClinicalTrials.gov processed this data on October 20, 2017
This information is provided by ClinicalTrials.gov.