Clinical Trial: A Study Exploring an Induction-Maintenance Kaletra-Based Therapy Versus a Sustiva-Based Regimen in Previously Non-Treated, HIV-1/HCV Co-Infected Subjects

This study is not yet open for patient recruitment.

Sponsored by: Abbott Laboratories
Information provided by: Abbott Laboratories

Purpose

The purpose of this study is to determine whether a simplified lopinavir/ritonavir-based therapy will continue to keep the viral load at very low levels after initial treatment with a combination of Kaletra (lopinavir/ritonavir) plus tenofovir and emtricitabine.
Condition Intervention Phase
HIV Infection
Hepatitis C
 Drug: Kaletra (lopinavir/ritonavir)
 Drug: Sustiva (efavirenz)
 Drug: Truvada (emtricitabine/tenofovir disoproxil fumarate)
Phase II

MedlinePlus related topics:  AIDS;   Hepatitis C

Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment

Official Title: A Randomized, Open-Label Study Assessing Safety, Tolerability and Efficacy of an Induction-Maintenance Treatment Strategy Including Lopinavir/Ritonavir Plus Tenofovir Disoproxil Fumarate and Emtricitabine Versus Efavirenz Plus Tenofovir Disoproxil Fumarate and Emtricitabine in Antiviral-naïve HIV-1/HCV Co-Infected Subjects

Eligibility

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Both
Criteria

Inclusion Criteria:

  • Subject is at least 18 years of age.
  • Subject''''s plasma HIV-1 RNA is >1000 copies/mL at screening and in the investigator''''s opinion, the subject requires antiretroviral therapy.
  • Subject is naive to antiretroviral therapy or has received <7 days total of any antiretroviral therapy >30 days prior to study drug administration.
  • Subject has chronic HCV based on detectable plasma HCV RNA level (>600 IU/mL) at screening.
  • Subject is not currently undergoing treatment of HCV infection and does not plan to initiate HCV treatment for the duration of this study.
  • If female, the results of a urine pregnancy test performed at screening and on Day-1/Baseline are both negative.
  • If female, subject is either not of childbearing potential, defined as postmenopausal for at least one year or surgically sterile (bilateral tubal ligation, bilateral oophorectomy or hysterectomy), or is of childbearing potential and practicing one of the following methods of birth control: condoms, sponge, foams, jellies, diaphragm or intrauterine device, a vasectomized partner or total abstinence from sexual intercourse.
  • Subject is not breastfeeding.
  • Subject''''s vital signs, physical examination and laboratory results do not exhibit evidence of acute illness.
  • Subject agrees not to take any drugs during the study, including over-the-counter medicines, vitamins, mineral supplements, herbal preparations, alcohol or recreational drugs without the knowledge and permission of the investigator.
  • Subject has not been treated for an active AIDS-defining opportunistic infection within 30 days of initiating study drug.
  • Subject has voluntarily signed and dated an informed consent from, approved by an Institutional Review Board (IRB)/Independent Ethics Committee (IEC), after the nature of the study has been explained and the subject has had the opportunity to ask questions. The informed consent must be signed before any study-specific procedures are performed.

Exclusion Criteria:

  • Subject has a history of an allergic reaction or significant sensitivity to lopinavir, ritonavir, tenofovir, emtricitabine, lamivudine, and efavirenz or to any inert materials contained in the study drug formulations.
  • Subject has a significant history of cardiac, renal, neurologic, psychiatric, oncologic or metabolic disease that would, in the opinion of the investigator, adversely affect his/her participation in this study.
  • Subject has chronic hepatic disease of any etiology other than HCV infection (including hemochromatosis, autoimmune hepatitis, Wilson''''s Disease, and hepatocellular carcinoma).
  • Subject has a liver biopsy result consistent with advanced chronic cirrhosis or a Child Pugh Score of "C".
  • Subject is currently taking or will require any drugs that are contraindicated or have significant pharmacokinetic interactions with study drugs during the course of the study. For complete information refer to the most current product label for locally approved prescribing information for lopinavir/ritonavir (Kaletra), efavirenz (Sustiva), tenofovir disoproxil fumarate (Viread), emtricitabine (Emtriva), co-formulated emtricitabine/tenofovir disoproxil fumarate (Truvada) and lamivudine (Epivir).
  • Subject has ongoing history of drug and/or alcohol abuse or psychiatric illness that in the investigator''''s opinion could preclude compliance with the protocol.
  • Subject has received any investigational drug or vaccine within 30 days prior to study drug administration.
  • The screening HIV-1 genotype resistance report suggests resistance or possible resistance to the study RTI(s) or lopinavir/ritonavir; Evidence of possible resistance to efavirenz: Presence of one of the following mutations: RT L1001, K103N, V106A or M, V108I, Y181C or I, Y188L, G190A or S, P225H, M230L: Evidence of possible resistance to emtricitabine or lamivudine: Presence of one of the following mutations; RTm184V or I: Evidence of possible resistance to tenofovir; Presence of RT K65R or insertion at codon 69, or presence of 2 or more of the following mutations: RTm41L, D67N, K70R, L210W, any change at T215, K219Q or Evidence of possible resistance to lopinavir/ritonavir: Presence of one or more of the following mutations; protease I47V or A, G48V, I50V, V82A or F or T or S, I84V, 190M or presence of 3 or more of the following mutations; protease L10F or I or R or V, K20M or R, L24I, V32I, L33F, M36I, M46I or L, F53L, any change at I54, A71V or T, G73S.
  • Screening laboratory analyses show any of the following abnormal laboratory results: Presence of hepatitis B surface antigen (HBsAg) or anti-HBcAB (Total Ig, Total Bilirubin >/= 2.5x upper limit of normal (ULN), Hemoglobin <8.0 g/dL, Absolute neutrophil count < 750 cells/uL, Platelet count < 50,000/mL, ALT (SGPT) or AST (SGOT) > 5.0x ULN, Creatinine > 1.5x ULN, Calculated creatinine clearance < 50 mL/min, PT > 3.0 seconds prolonged from the ULN.
  • For any reason, subject is considered by the investigator to be an unsuitable candidate to participate in the study.

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00121017

Debbie Tokimoto, M.P.H.      847-938-9415    debbie.tokimoto@abbott.com

Virginia
      Hampton Roads Medical Specialists, Hampton,  Virginia,  United States
 757-838-8677  Ext. 15 
Stephen Green, M.D.,  Principal Investigator

More Information

Study ID Numbers:  M05-731
Record last reviewed:  July 2005
Last Updated:  July 25, 2005
Record first received:  July 20, 2005
ClinicalTrials.gov Identifier:  NCT00121017
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-07-26

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