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

HIV-1 Infection Clinical Trial

— BocepreVIH  

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01335529
• Other study ID #: ANRS HC27 BOCEPREVIH
• Status: Completed
• Phase: Phase 2
• First received: March 25, 2011
• Last updated: October 10, 2014
• Start date: May 2011
• Est. completion date: May 2014

Study information

• Verified date: October 2014
• Source: French National Institute for Health and Medical Research-French National Agency for Research on AIDS and Viral Hepatitis (Inserm-ANRS)
• Contact: n/a
• Is FDA regulated: No
• Health authority: France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 69
• Est. completion date: May 2014
• Est. primary completion date: May 2014
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

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

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Coinfection
• HCV Coinfection
• HIV-1 Infection
• Infection

Intervention

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.

Locations

Country	Name	City	State
France	CHU Sainte Marguerite	Marseille

Sponsors (3)

Lead Sponsor	Collaborator
French National Institute for Health and Medical Research-French National Agency for Research on AIDS and Viral Hepatitis (Inserm-ANRS)	Merck Sharp & Dohme Corp., Rennes University Hospital

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Sustained Virologic Response	HCV-RNA measured 24 weeks after the end of the HCV treatment (W72 or W96)	Week 72 or Week 96 (W72 or W96)	No
Secondary	HCV viral load	HCV-RNA	W4, W8, W12, W16, W28, W36 and at treatment completion at W48/72	No
Secondary	Predictive factors of Sustained virologic Response (SVR)	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	Baseline	No
Secondary	HIV virologic endpoints	HIV-RNA; CD4 and CD8 count	W4, W8, W12, W16, W20, W24, W28, W32, W36, W40, W44, W48, W60, W72 and W84, W96 if treatment duration is 72 weeks	No
Secondary	Residual plasmatic concentration (Cres) of Ribavirin		W4 and W8	No
Secondary	Hepatic factors: liver fibrosis score	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).	Screen, W4, W8, W16, W28, W48, W72, W96.	No
Secondary	Alcohol consumption		W4, W8, W16, W28, W48, W72, W96	No
Secondary	Evaluation of Pharmacokinetic parameters of anti-retroviral treatments	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.	Day 0, W8	No
Secondary	Clinical and biological adverse events		Up to 24 weeks after treatment completion (W72 or W96)	Yes
Secondary	Number of participants classified by virologic failure type: non responder, relapser, null responder	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	W8, W12, W16, W28, W48, W72, W96	No
Secondary	ITPA gene polymorphism	The relation between ITPA gene polymorphism and onset of haemolytic anaemia will be analysed.	Day 0	No
Secondary	CYP3A4 Polymorphism	Evaluation of Pharmacokinetic parameters (Cres, Cmax, AUC) of Boceprevir at W8 in a sub-group of subjects, according to antiretroviral treatment and CYP3A4 polymorphism.	W8	No
Secondary	Maximal Concentration (Cmax) of antiretroviral treatments	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.	Day 0 and W8	No
Secondary	Area Under the Curve (AUC) of antiretrovirals	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.	Day 0 and W8	No
Secondary	Insulin resistance	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).	at W4, W8, W16, W28, W48, W72, W96	No
Secondary	Metabolic syndrome	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).	W4, W8, W16, W28, W48, W72, W96	No
Secondary	Reasons and dates of treatment discontinuation		Up to W72	Yes
Secondary	Perceived symptoms	Perceived symptoms will be assessed on "AC24 French AIDS scale"	Day 0, W28, W48, W72, W96	Yes
Secondary	French AIDS questionnaire of compliance		W0, W28, W48, W72	Yes
Secondary	Tobacco consumption		W4, W8, W16, W28, W48, W72, W96	No
Secondary	Cannabis consumption		W4, W8, W16, W28, W48, W72, W96	No
Secondary	Intravenous/nasal drugs consumption		W4, W8, W16, W28, W48, W72, W96	No
Secondary	Residual Concentration (Cres) of atazanavir boosted or not by ritonavir	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).	At screening day, at W48 and in the case of virological rebound	No
Secondary	Residual concentration (Cres) of ritonavir	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).	At screening day, at W48 and in the case of virological rebound	No