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Boceprevir in HIV-HCV Coinfected Patients Who Have Failed to a Previous Therapy With Peg-Interferon/Ribavirin (BocepreVIH)

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ClinicalTrials.gov Identifier: NCT01335529
Recruitment Status : Completed
First Posted : April 14, 2011
Last Update Posted : October 13, 2014
Sponsor:
Collaborators:
Rennes University Hospital
Merck Sharp & Dohme Corp.
Information provided by (Responsible Party):
French National Institute for Health and Medical Research-French National Agency for Research on AIDS and Viral Hepatitis (Inserm-ANRS)

Study Description
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Brief Summary:

The majority of Human immunodeficiency Virus (HIV)/Hepatitis C Virus (HCV) co-infected patients are non responders after 48 weeks of the current standard-of-care with Peg-Interferon/Ribavirin. The results of re-treatment are disappointing. The addition of Boceprevir to the current standard-of-care has been shown to increase the efficacy of therapy in HCV mono-infected patients previously treated with a bi-therapy. Knowing that HIV/HCV co-infected patients are subject to more rapid hepatic fibrosis as well as to increased risks of cirrhosis, end-stage liver disease and hepatocellular carcinoma, it is important to improve the response rate of the re-treatment of hepatitis C in these patients.

The aim of this pilot study is to evaluate the efficacy and safety of Boceprevir in combination with Peg-Interferon alfa 2b plus ribavirin, in patients co-infected with HIV and chronic genotype 1 HCV, and previously treated with Peg-Interferon/Ribavirin. 80 subjects will be enrolled. The primary endpoint will be the Sustained Virologic Response (SVR) defined as undetectable HCV-RNA at Week 24 after the end of therapy.


Condition or disease Intervention/treatment Phase
HCV Coinfection HIV-1 Infection Drug: Boceprevir, Peg-interferon alfa 2b and Ribavirin Phase 2

Detailed Description:

The majority of HIV/HCV co-infected patients are non responders after 48 weeks of the current standard-of-care with Peg-Interferon/Ribavirin. The results of re-treatment are disappointing. The addition of Boceprevir to the current standard-of-care has been shown to increase the efficacy of therapy in HCV mono-infected patients previously treated with a bi-therapy. Knowing that HIV/HCV co-infected patients are subject to more rapid hepatic fibrosis as well as to increased risks of cirrhosis, end-stage liver disease and hepatocellular carcinoma, it is important to improve the response rate of the re-treatment of hepatitis C in these patients.

Subjects enrolled in this trial will have many predictive factors of failure: HIV co-infection, previous failure to Peg-Interferon/Ribavirin, HCV genotype 1 infection. One study reported a SVR rate of 9% after re-treatment with Peg-Interferon/Ribavirin in such patients. Another trial has shown a substantial increase of the response rate with a tri-therapy in HCV mono-infected patients.

The investigators propose to carry out a multicentric, national, non-randomized phase II trial in 80 patients.

The proportion of patients with F4 cirrhosis will have to be inferior to 50% of enrolled subjects.

The number of null responders to a previous treatment (HCV RNA drop < 2 log10 at W12) and without F4 cirrhosis will have to be lower or equal to 20.

The primary objective of the study is to estimate, in Genotype 1 - HCV/HIV co-infected patients, non responders to a previous therapy with Peg-Interferon/Ribavirin, the rate of SVR after 48 or 72 weeks of a three-drug regimen containing Peg-Interferon, Ribavirin and Boceprevir according to the Virologic Response and to compare the SVR rate to a threshold rate 20%, lowest rate to consider a therapeutic benefit in this population.

A pharmacokinetic sub-study including 30 patients will be performed to estimate pharmacokinetic parameters of antiretroviral treatment (Atazanavir combined with Ritonavir, Raltegravir, Tenofovir) in combination with anti HCV treatment at baseline and W8 and pharmacokinetic parameters of Boceprevir at W8.


Study Design
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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 69 participants
Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Pilot Study to Assess the Efficacy and Safety of Boceprevir, in Combination With Peg-Interferon Alfa and Ribavirin, in Patients With HCV/HIV Co-infection Who Have Failed to a Previous Therapy With Peg-Interferon/Ribavirin
Study Start Date : May 2011
Actual Primary Completion Date : May 2014
Actual Study Completion Date : May 2014

Resource links provided by the National Library of Medicine

MedlinePlus related topics: HIV/AIDS
U.S. FDA Resources

Arms and Interventions
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Arm Intervention/treatment
Experimental: Boceprevir, PegIFN alfa 2b, Ribavirin

Standard Treatment :

  • Peg-Interferon (PegIFN) alfa 2b by subcutaneous injection 1,5 µg/kg/week
  • Ribavirin capsules 200mg: dosage delivered in weight categories (< 65 kg: 800 mg ; 65-80 kg: 1000 mg; 81-105 kg: 1200mg; > 105 kg: 1400mg)

Three-drug-regimen:

  • Peg-Interferon alfa 2b by subcutaneous injection 1,5 µg/kg/week
  • Ribavirin capsules 200mg: dosage delivered in weight categories like in standard treatment
  • Boceprevir tablets 200mg: 800 mg 3 times a day (2400 mg/j) with food
 Drug: Boceprevir, Peg-interferon alfa 2b and Ribavirin
  • Screen period from Week-8
  • Standard treatment from day 0 to week 4 (W4)
  • Three-drug-regimen (Boceprevir introduction) from W4 to W8

  • HCV RNA determination at W8 determines treatment group and participation duration:

    • If undetectable HCV RNA at W8, it is a complete virological response: 3 drug-regimen is continued until W48, then there is a follow-up period up to W72 and SVR analysis,
    • If HCV RNA ≤ 1000IU/mL at W8, it is an incomplete virological response. The 3-drug-regimen is continued until W72, when another analysis is done.
Other Names:
  • ViraferonPeg
  • Rebetol


Outcome Measures
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Primary Outcome Measures :
  1. Sustained Virologic Response [ Time Frame: Week 72 or Week 96 (W72 or W96) ]
    HCV-RNA measured 24 weeks after the end of the HCV treatment (W72 or W96)


Secondary Outcome Measures :
  1. HCV viral load [ Time Frame: W4, W8, W12, W16, W28, W36 and at treatment completion at W48/72 ]
    HCV-RNA

  2. Predictive factors of Sustained virologic Response (SVR) [ Time Frame: Baseline ]
    • Sex
    • Age (< vs ≥ 40 years)
    • Risk factor of HIV infection (drug consumer versus other risk factors)
    • Risk factor of HCV infection (drug consumer versus other risk factors)
    • Ethnic origin (Africano-American or Subsaharian-African or West Indies versus others)
    • CDC stade (C vs. A-B)
    • CD4 number (< vs. ≥ 350/mm3)
    • HCV viral load (< versus ≥ 800 000 UI/ml)
    • HCV genotype (1a versus 1b)
    • Cirrhosis (F4 versus no cirrhosis)
    • Alcohol, tobacco, cannabis, intravenous/nasal drugs consumption
    • IL28 gene polymorphism

  3. HIV virologic endpoints [ Time Frame: W4, W8, W12, W16, W20, W24, W28, W32, W36, W40, W44, W48, W60, W72 and W84, W96 if treatment duration is 72 weeks ]
    • HIV-RNA
    • CD4 and CD8 count

  4. Residual plasmatic concentration (Cres) of Ribavirin [ Time Frame: W4 and W8 ]
  5. Hepatic factors: liver fibrosis score [ Time Frame: Screen, W4, W8, W16, W28, W48, W72, W96. ]
    Evolution of liver fibrosis between baseline and 24 weeks post-treatment, according to baseline value and Sustained Virologic Response (at W4, W8, W16, W28, W48/72 and 24 weeks post-treatment).

  6. Alcohol consumption [ Time Frame: W4, W8, W16, W28, W48, W72, W96 ]
  7. Evaluation of Pharmacokinetic parameters of anti-retroviral treatments [ Time Frame: Day 0, W8 ]
    Pharmacokinetic parameters (Cres, Cmax, AUC) of anti-retroviral treatments before (baseline) and after (W8) the starting of Boceprevir combination in a sub-group of subjects and according to UGTA1 polymorphism.

  8. Clinical and biological adverse events [ Time Frame: Up to 24 weeks after treatment completion (W72 or W96) ]
  9. Number of participants classified by virologic failure type: non responder, relapser, null responder [ Time Frame: W8, W12, W16, W28, W48, W72, W96 ]
    • Relapse patients: undetectable HCV RNA at the end of therapy, becoming detectable after treatment cessation.
    • Break-through patients: undetectable HCV-RNA at least once during treatment, becoming detectable before treatment cessation.
    • Non-responder patients: detectable HCV-RNA at W24, never achieved undetectable and HCV RNA drop ≥ 2 log at W12.
    • Null responder patients: HCV RNA drop < 2 log at W12

  10. ITPA gene polymorphism [ Time Frame: Day 0 ]
    The relation between ITPA gene polymorphism and onset of haemolytic anaemia will be analysed.

  11. CYP3A4 Polymorphism [ Time Frame: W8 ]
    Evaluation of Pharmacokinetic parameters (Cres, Cmax, AUC) of Boceprevir at W8 in a sub-group of subjects, according to antiretroviral treatment and CYP3A4 polymorphism.

  12. Maximal Concentration (Cmax) of antiretroviral treatments [ Time Frame: Day 0 and W8 ]
    Evaluation of Pharmacokinetic parameters (Cres, Cmax, AUC) of anti-retroviral treatments before (baseline) and after (W8) the starting of Boceprevir combination in a sub-group of subjects and according to UGTA1 polymorphism.

  13. Area Under the Curve (AUC) of antiretrovirals [ Time Frame: Day 0 and W8 ]
    Evaluation of pharmacokinetic parameters (Cres, Cmax, AUC) of anti-retroviral treatments before (baseline) and after (W8) the starting of Boceprevir combination in a sub-group of subjects and according to UGTA1 polymorphism.

  14. Insulin resistance [ Time Frame: at W4, W8, W16, W28, W48, W72, W96 ]
    Evolution of insulin resistance between baseline and 24 weeks post-treatment according to baseline value and Sustained Virologic Response (at W4, W8, W16, W28, W48/72 and 24 weeks post-treatment).

  15. Metabolic syndrome [ Time Frame: W4, W8, W16, W28, W48, W72, W96 ]
    Evaluation of metabolic syndroms parameters according to baseline value and Sustained Virologic Response (at W4, W8, W16, W28, W48/72 and 24 weeks post-treatment).

  16. Reasons and dates of treatment discontinuation [ Time Frame: Up to W72 ]
  17. Perceived symptoms [ Time Frame: Day 0, W28, W48, W72, W96 ]
    Perceived symptoms will be assessed on "AC24 French AIDS scale"

  18. French AIDS questionnaire of compliance [ Time Frame: W0, W28, W48, W72 ]
  19. Tobacco consumption [ Time Frame: W4, W8, W16, W28, W48, W72, W96 ]
  20. Cannabis consumption [ Time Frame: W4, W8, W16, W28, W48, W72, W96 ]
  21. Intravenous/nasal drugs consumption [ Time Frame: W4, W8, W16, W28, W48, W72, W96 ]
  22. Residual Concentration (Cres) of atazanavir boosted or not by ritonavir [ Time Frame: At screening day, at W48 and in the case of virological rebound ]
    Measure of residual concentration of atazanavir for patients treated by atazanavir boosted or not by ritonavir at screening day, at W48 and in case of virological rebound (HIV and HCV).

  23. Residual concentration (Cres) of ritonavir [ Time Frame: At screening day, at W48 and in the case of virological rebound ]
    Measure of residual concentration of ritonavir for patients treated by atazanavir boosted by ritonavir at screening day, at W48 and in case of virological rebound (HIV and HCV).


Eligibility Criteria
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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Adult ≥18 years
  • HIV-1 infection
  • Infection to genotype 1 HCV only
  • Patients must have received at least 12 weeks of treatment with Peg-Interferon alfa 2a ≥ 135 µg / once weekly or Peg-Interferon alfa 2b ≥ 1,0 µg/kg/ once weekly + Ribavirin ≥ 600 mg daily and must have failed to treatment.
  • Anti-HCV treatment stopped for at least 6 months

  • Patients must be already treated at screen since at least 3 months with a stable combination of antiretroviral treatment as following:

    • Either tenofovir - emtricitabine, and atazanavir in combination with ritonavir
    • Or tenofovir - emtricitabine, and raltegravir
    • If patients cannot receive neither of the two antiretroviral regimens proposed, for virologic, safety or toxicity reasons, patients could receive any effective antiretroviral therapy including : tenofovir, emtricitabine, lamivudine, atazanavir alone or in combination with ritonavir, raltegravir, abacavir. These patients are not allowed to take part in the pharmacokinetic sub-study.
  • CD4 > 200/mm3 et >15%, at screen
  • HIV-RNA < 50 copies/ml since at least 6 months at screen
  • ≥ 40 Kg and ≤ 125 Kg
  • Patients with any fibrosis grade. Proportion of F4 subjects should not excess 50% of the overall subjects.
  • Male and female subjects must agree to use acceptable methods of contraception 1 month prior to starting the study treatment and to continue until 7 months after the last doses of study drugs for male subjects and their partner(s), 4 months for female subjects.
  • Subjects must be willing to give written informed consent for principal study (signed at least at screen visit and prior to any study investigation)and + for the pharmacokinetic sub-study (for the concerned centers).
  • Subjects must be willing to give written informed consent for biological collection.
  • Subjects must be willing to give written informed consent for treatment of genetics data.
  • Subjects affiliated or beneficiary to a medical insurance.

Exclusion Criteria:

History:

  • Patients with cirrhosis (F4) and nul responders to prior treatment
  • Cirrhosis classified Child-Pugh B or C or history of decompensated cirrhosis of the liver. If Child A classification, significant varicose veins (grade 2 or 3) observed with a fibroscopy realized for < 3 years.
  • History of ocular neuritis, retinal disorders, transplant
  • Opportunistic infections (classification C), active or occurred within the 6 months prior to baseline.
  • History of neoplasia within the last 5 years, except cutaneous basocellular carcinoma, recovering Kaposi's sarcoma, in situ cervical or anal canal cancer.

Current condition:

  • Co-infection with Hepatitis B virus
  • Pregnancy and lactation
  • Cardiac or severe pulmonary disease
  • Untreated dysthyroidism
  • Autoimmune disease contraindicating to an interferon treatment
  • Severe haemoglobinopathies
  • Any condition needing a systemic corticotherapy or an immunosuppressive treatment
  • Evolutive current malignancy, including hepatocarcinoma which should be specifically controlled prior to baseline.
  • Alcohol consumption which may disturb the study participation according to the investigator
  • Drug addiction which may disturb the study participation according to the investigator. Patients taking part to a substitution program with methadone or buprenorphine are allowed to be enrolled in the study.

Biological criteria:

• Haemoglobin < 12 g/dL (female) or < 13g/dL (male), Platelets < 90 000/mm3, Neutrophil count < 1500/mm3, Renal failure defined as creatinine clearance < 50ml/min, Uncontrolled thyroid function, HbA1c ≥ 7% in case of diabetes

Criteria related to study drugs

  • Contra-indication to Ribavirin, interferon treatment including psychiatric contra-indications.
  • History of discontinuation for intolerance to anti-HCV treatment.Patients with a history of discontinuation for intolerance, especially anaemia or leuconeutropenia, and who were not treated with hematopoietic growth factor, are eligible
  • Concomitant medication which may interfere with Boceprevir, atazanavir, ritonavir and raltegravir pharmacokinetic
  • St.John's-wort consumption
Contacts and Locations
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Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01335529


Locations
France
CHU Sainte Marguerite
Marseille, France, 13009
Sponsors and Collaborators
French National Institute for Health and Medical Research-French National Agency for Research on AIDS and Viral Hepatitis (Inserm-ANRS)
Rennes University Hospital
Merck Sharp & Dohme Corp.
Investigators
Principal Investigator: Isabelle Poizot-Martin, MD Marseille University Hospital
Study Chair: Eric Bellissant, MD, PhD Rennes University Hospital
More Information
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Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

Responsible Party: French National Institute for Health and Medical Research-French National Agency for Research on AIDS and Viral Hepatitis (Inserm-ANRS)
ClinicalTrials.gov Identifier: NCT01335529     History of Changes
Other Study ID Numbers: ANRS HC27 BOCEPREVIH
First Posted: April 14, 2011    Key Record Dates
Last Update Posted: October 13, 2014
Last Verified: October 2014

Keywords provided by French National Institute for Health and Medical Research-French National Agency for Research on AIDS and Viral Hepatitis (Inserm-ANRS):
HCV infection
HIV-1 infection

Additional relevant MeSH terms:
Infection
Communicable Diseases
Coinfection
Virus Diseases
Parasitic Diseases
Interferons
Ribavirin
Interferon-alpha
 Peginterferon alfa-2b
Antineoplastic Agents
Antiviral Agents
Anti-Infective Agents
Antimetabolites
Molecular Mechanisms of Pharmacological Action
Immunologic Factors
Physiological Effects of Drugs