Optimizing Treatment for Treatment-Experienced, HIV-Infected People

This study has been completed.
Sponsor:
Collaborator:
AIDS Clinical Trials Group
Information provided by (Responsible Party):
National Institute of Allergy and Infectious Diseases (NIAID)
ClinicalTrials.gov Identifier:
NCT00537394
First received: September 27, 2007
Last updated: July 14, 2014
Last verified: July 2014
  Purpose

The goal of anti-HIV therapy is to prevent HIV from replicating. Long-term control of HIV requires at least two anti-HIV drugs that are active against the virus. Drug resistance is a problem for many treatment-experienced, HIV-infected people. The purpose of this study was to determine the benefit of adding a nucleoside reverse transcriptase inhibitor (NRTI) to a new anti-HIV drug regimen for the suppression of HIV.


Condition Intervention Phase
HIV Infections
Drug: Enfuvirtide
Drug: Raltegravir
Drug: Darunavir
Drug: Tipranavir
Drug: Etravirine
Drug: Maraviroc
Phase 3

National Institute of Allergy and Infectious Diseases (NIAID) has indicated that access to an investigational treatment associated with this study is available outside the clinical trial.  

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: The Optimized Treatment That Includes or Omits NRTIs Trial: A Randomized Strategy Study for HIV-1-Infected Treatment-Experienced Subjects Using the cPSS to Select an Effective Regimen

Resource links provided by NLM:


Further study details as provided by National Institute of Allergy and Infectious Diseases (NIAID):

Primary Outcome Measures:
  • Percent of Participants With Regimen Failure, Defined as a Confirmed Virologic Failure or Discontinuation of Randomized NRTI Component of Study Treatment [ Time Frame: From study entry to end of Week 48 evaluation window ] [ Designated as safety issue: No ]
    Virologic failure defined as confirmed plasma HIV-1 RNA meeting 1 of the following 4 criteria: < 1.0 log10 copies/mL reduction from baseline level and >= 200 copies/mL at or after week 12 evaluation; >= 200 copies/mL after 1 measurement < 200 copies/mL; absence of any values < 200 copies/mL by and including week 24 evaluation; >= 200 copies/mL at week 48 evaluation. Discontinuation of Randomized NRTI component of Study Treatment is defined as permanently stopping all NRTIs among those randomized to add NRTIs, or starting any NRTI among those randomized to omit NRTIs. Subjects leaving the study for reasons other than death, relocation, incarceration, or site closure were reviewed for the discontinuation outcome by a blinded, independent panel. Additionally, any participant failing to start study treatment after randomization and prior to closure was also reviewed. Results report percent of participants reaching regimen failure outcome by week 48 evaluation using Kaplan-Meier method.


Secondary Outcome Measures:
  • Time From Treatment Dispensation to First Grade 3 or Higher (and at Least One Grade Higher Than Baseline) Signs/Symptom or Laboratory Abnormality [ Time Frame: From treatment dispensation to week 96 study visit ] [ Designated as safety issue: Yes ]
    Events following permanent discontinuation of NRTI assignment are excluded (i.e. censoring at time of this event, if applicable).

  • Time From Treatment Dispensation to First Study ARV Modification (Excluding NRTIs, if Applicable) [ Time Frame: From treatment dispensation to week 96 study visit ] [ Designated as safety issue: No ]
  • Time From Randomization to Discontinuation of Randomized NRTI Component of Study Treatment [ Time Frame: From randomization to week 96 study visit ] [ Designated as safety issue: No ]
    Discontinuation of Randomized NRTI component of Study Treatment is defined as permanently stopping all NRTIs among those randomized to add NRTIs, or starting any NRTI among those randomized to omit NRTIs. Subjects leaving the study for reasons other than death, relocation, incarceration, or site closure were reviewed for meeting this outcome by a blinded, independent panel. Additionally, any participant failing to start study treatment after randomization and prior to closure was also reviewed.

  • Time From Randomization to Confirmed Virological Failure [ Time Frame: From randomization to week 96 study visit ] [ Designated as safety issue: No ]
    Virologic failure defined as confirmed (two consecutive) plasma HIV-1 RNA meeting 1 of the following 4 criteria: < 1.0 log10 copies/mL reduction from baseline level and >= 200 copies/mL at or after week 12 evaluation; >= 200 copies/mL after 1 measurement < 200 copies/mL; absence of any values < 200 copies/mL by and including week 24 evaluation; >= 200 copies/mL at week 48 evaluation.

  • Participants With Plasma HIV-1 Viral Load < 50 Copies/ml [ Time Frame: At Weeks 24, 48, 96 ] [ Designated as safety issue: No ]
    Number of participants with plasma HIV-1 Viral load < 50 copies/mL at study visit weeks 24 and 48. Closest observed result between 20 and up to 30 weeks (for week 24), and between 42 and up to 54 (for week 48) used if multiple results available. Missing values excluded.

  • Change in Plasma HIV-1 Viral Load From Baseline to Week 1 [ Time Frame: From baseline to Week 1 evaluation ] [ Designated as safety issue: No ]
    Method of Kaplan and Meier used to accommodate left-censoring for those whose week 1 levels < 50 copies/mL.

  • Change in Summarized Quality of Life Score [ Time Frame: At study entry and Weeks 24, 48, 96 ] [ Designated as safety issue: No ]
    Quality-of-life score at each evaluation based upon a single question assessing participants' self-report of general health with a range of 0 (representing worst health status) to 100 (representing perfect health).

  • Number of Participants Self-reporting Non-adherence to Assigned Study ARVS (Excluding NRTIs, if Applicable) [ Time Frame: At Weeks 24 and 48 ] [ Designated as safety issue: No ]
    Results represent self-report of non-adherence during the 4-day period prior to the outcome evaluation visit. Participants in follow-up for whom these data are missing for any reason are inferred as not-adherent.

  • Change in Cardiovascular Risk Score From Baseline [ Time Frame: At Weeks 24, 48, and 96 ] [ Designated as safety issue: No ]
    Cardiovascular risk score defined by Framingham

  • Change in CD4 Count From Baseline [ Time Frame: From study entry to Weeks 48 and 96 ] [ Designated as safety issue: No ]
    Baseline CD4 calculated as average of pre-entry and entry values. Closest observed result between 42 and up to 54 weeks (for week 48), used if multiple results available.

  • Time From Randomization to Serious Non-AIDS-defining Events [ Time Frame: From randomization to week 96 study visit ] [ Designated as safety issue: Yes ]
  • Change in Virus Co-receptor Tropism Among Those With R5-only Tropic Virus at Study Entry [ Time Frame: From study entry to time of confirmed virological failure ] [ Designated as safety issue: No ]
    HIV Co-receptor tropism test result of either dual/mixed or evidence of X4 using virus from sample collected at confirmed virologic failure.

  • Change in Fasting Non-HDL Cholesterol From Baseline [ Time Frame: From study entry to Weeks 24, 48 ] [ Designated as safety issue: No ]
    Fasting non-HDL cholesterol calculated from difference between fasting total cholesterol and fasting HDL level. Missing values and non-fasting values excluded.

  • Percent of Participants With Newly Acquired HIV Drug Resistance Between Study Entry and Confirmed Virologic Failure [ Time Frame: Between baseline and confirmed virologic failure ] [ Designated as safety issue: No ]
    Defined among the subgroup of participants experiencing the outcome of confirmed virologic failure. Newly acquired HIV drug resistance is defined as one or more ARVs with partial resistance when pre-entry resistance was fully sensitive or resistant when pre-entry resistance was fully sensitive or partially sensitive.


Enrollment: 517
Study Start Date: January 2008
Study Completion Date: April 2013
Primary Completion Date: May 2012 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: A
Regimen with higher predicted activity assigned by the study plus at least 2 NRTIs (personalized choice from expert recommendation) for 96 weeks. A 3-4 drug regimen will be selected from the drugs listed to the right.
Drug: Enfuvirtide
90mg subcutaneously twice daily
Drug: Raltegravir
400 mg twice daily
Drug: Darunavir
Two 300-mg tablets twice daily, given with ritonavir 100mg twice daily (ritonavir not provided by the study)
Drug: Tipranavir
Two 250-mg capsules twice daily, given with ritonavir 100mg twice daily (ritonavir not provided by the study)
Drug: Etravirine
Two 100-mg tablets twice daily
Drug: Maraviroc
Dosage dependent on regimen in which maraviroc is included
Experimental: B
Regimen with higher predicted activity assigned by the study without NRTIs for 96 weeks. A 3-4 drug regimen will be selected from the drugs listed to the right.
Drug: Enfuvirtide
90mg subcutaneously twice daily
Drug: Raltegravir
400 mg twice daily
Drug: Darunavir
Two 300-mg tablets twice daily, given with ritonavir 100mg twice daily (ritonavir not provided by the study)
Drug: Tipranavir
Two 250-mg capsules twice daily, given with ritonavir 100mg twice daily (ritonavir not provided by the study)
Drug: Etravirine
Two 100-mg tablets twice daily
Drug: Maraviroc
Dosage dependent on regimen in which maraviroc is included
C
Regimen with lower predicted activity assigned plus at least 2 NRTIs (personalized choice from expert recommendation) for 96 weeks. A 3-4 drug regimen will be selected from the drugs listed to the right.
Drug: Enfuvirtide
90mg subcutaneously twice daily
Drug: Raltegravir
400 mg twice daily
Drug: Darunavir
Two 300-mg tablets twice daily, given with ritonavir 100mg twice daily (ritonavir not provided by the study)
Drug: Tipranavir
Two 250-mg capsules twice daily, given with ritonavir 100mg twice daily (ritonavir not provided by the study)
Drug: Etravirine
Two 100-mg tablets twice daily
Drug: Maraviroc
Dosage dependent on regimen in which maraviroc is included

Detailed Description:

Two or more fully active antiretrovirals (ARVs) are recommended for successful suppression of HIV. In people infected with resistant HIV virus, finding two drugs that are fully active against HIV can be a challenge. However, the new generation of anti-HIV drugs has been designed to suppress drug-resistant HIV. These drugs include the FDA-approved protease inhibitors (PIs) darunavir and tipranavir, the investigational non-nucleoside transcriptase inhibitor (nNRTI) etravirine, the FDA-approved fusion inhibitor enfuvirtide, the recently FDA-approved CCR5 inhibitor maraviroc, and the investigational integrase inhibitor raltegravir. Also, it is not yet known whether multiple, partially-active drugs have the same rate of success in suppressing HIV. The purpose of this study was to use HIV resistance testing to predict the potency of a suggested ARV regimen using second generation ARVs and determine if the benefits of adding NRTIs to this new drug regimen outweigh the risks of drug toxicity and pill burden. All participants had treatment experience or resistance to NRTIs, nNRTIs, and PIs, and received novel agents.

An active screening period occurred for up to 75 days for all participants, and study participation lasted an additional 96 weeks for those who qualified for either randomization or assignment (i.e. not randomized), to the study intervention. During active screening, all participants remained on their current drug regimen. During screening, phenotypic and genotypic HIV resistance tests were performed on participants' blood samples, as well as a coreceptor tropism assay. Using this information and medication history, the study team determined the best new regimen options for each participant. Each clinician, along with the study participant, then chose a new regimen based on the recommendations of the study team and the participant's preference.

Evaluation for study outcomes began when participants started their new regimen as assigned by either randomization or determined assignment. Stratification between Arms A (Add NRTIs) and B (Omit NRTIs) or Arm C (Non-randomized to Add NRTIs) was based on predicted activity of the new regimen. Those assigned to a regimen with higher predicted activity were randomly assigned to Arm A (Add NRTIs) or B (Omit NRTIs); those assigned a regimen predicted to have lower activity were not randomized, but were assigned to Arm C (Add NRTIs).

Participants in Arms A and C will take their new assigned study regimen plus at least 2 NRTIs (personalized from expert recommendation and choice by local provider and participant) for 96 weeks. Participants in Arm B will take their new assigned study regimen with no NRTIs for 96 weeks. Participants in all arms who meet the primary efficacy outcome of regimen failure will remain in the study in order to be followed for important secondary outcomes.

All participants will have 13 clinical visits. At each visit, blood collection will occur. At some visits, urine collection and quality of life and adherence questionnaires will occur. A neurocognitive assessment will be done for all participants at time of starting the new study regimen. Participants may also consent to have cerebrospinal fluid collected via lumbar puncture following study treatment assignment and/or at Week 24. Those participants who consent to cerebrospinal fluid collection will also have neurocognitive assessments at the times of collections. Participants will be responsible for obtaining certain ARVs not provided by the study, including the ARVs they during the active screening period.

The primary study objectives and comparisons relate to the randomized arms, and therefore, results will not be initially provided for the non-randomized arm (C). The primary completion date of 5/31/12 reflects follow-up through study visit window for week 48, and therefore the initial results submission pertains to data from the randomized arms up to the primary outcome timepoint at week 48. All secondary outcomes and AE measured after week 48 will be reported when available.

  Eligibility

Ages Eligible for Study:   16 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • HIV-1 infection
  • Triple-class drug experience or resistance. More information on this criterion can be found in the protocol.
  • Currently on a failing PI-containing regimen that includes 2 other ARVs with no regimen change for 8 weeks prior to study screening
  • HIV viral load of 1000 copies/ml or more
  • Hepatitis B surface antigen negative within 90 days of study entry
  • Able to obtain NRTIs and ritonavir and have required ARVs at time of starting study intervention
  • Willing to use acceptable forms of contraception
  • Parent or legal guardian willing to provide consent, if applicable
  • CD4 count result from a specimen drawn within 120 days prior to study entry
  • If any previous HIV-1 viral co-receptor tropism result is available, then most recent specimen date and the tropism result of that specimen AND specimen date and tropism result of any test with either X4 or D/M result, if different from the first specimen, must be available

Inclusion Criteria continued:

  • Receipt of successful phenotype/genotype resistance results within 105 days prior to study treatment intervention assignment
  • Study team identification of a study regimen and at least 2 NRTIs for participant to take
  • Certain abnormal laboratory values. More information on this criterion can be found in the protocol.

Exclusion Criteria:

  • Chronic, active hepatitis B virus infection (hepatitis B surface antigen positive or HBV DNA positive)
  • Taking certain medications. More information on this criterion can be found in the protocol.
  • Known allergy/sensitivity to components of two or more of the study-provided drugs or their formulations. For maraviroc, this includes hypersensitivity or history of allergy to soy lecithin or peanuts.
  • Active drug or alcohol use that, in the opinion of the investigator, may interfere with the study
  • Pregnancy or breastfeeding
  • Use of any immunomodulator (interferons, interleukins, systemic corticosteroids, or cyclosporine), vaccine, or investigational therapy within 30 days prior to study treatment allocation/assignment
  • Require certain medications prohibited with study treatment
  • Serious illness requiring systemic treatment or hospitalization. Participants who complete therapy or are clinically stable on therapy for at least 14 days prior to study treatment allocation are not excluded.
  Contacts and Locations
Choosing 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: NCT00537394

  Hide Study Locations
Locations
United States, Alabama
Alabama Therapeutics CRS
Birmingham, Alabama, United States, 35294-2050
United States, California
Miller Children's Hosp. Long Beach CA NICHD CRS
Long Beach, California, United States, 90806
University of Southern California CRS
Los Angeles, California, United States, 90033
UCLA CARE Center CRS
Los Angeles, California, United States, 90035
UCLA-Los Angeles/Brazil AIDS Consortium (LABAC) CRS
Los Angeles, California, United States, 90095-1752
Usc La Nichd Crs
Los Angeles, California, United States, 90033
Stanford AIDS Clinical Trials Unit CRS
Palo Alto, California, United States, 94304-5350
UCSD Antiviral Research Center CRS
San Diego, California, United States, 92103
Ucsf Hiv/Aids Crs
San Francisco, California, United States, 94110
Univ. of California San Francisco NICHD CRS
San Francisco, California, United States, 94143
United States, Colorado
University of Colorado Hospital CRS
Aurora, Colorado, United States, 80045
Denver Public Health CRS
Denver, Colorado, United States, 80204
United States, District of Columbia
Howard Univ. Washington DC NICHD CRS
Washington, District of Columbia, United States, 20060
Georgetown University CRS (GU CRS)
Washington, District of Columbia, United States, 20007
Children's National Med. Ctr. ATN CRS
Washington, District of Columbia, United States, 20010
United States, Florida
Pediatric Perinatal HIV Clinical Trials Unit CRS
Miami, Florida, United States, 33136
United States, Georgia
The Ponce de Leon Center CRS
Atlanta, Georgia, United States, 30308-2012
United States, Illinois
Rush University CRS
Chicago, Illinois, United States, 60612
Northwestern University CRS
Chicago, Illinois, United States, 60611
United States, Louisiana
Tulane Univ. New Orleans NICHD CRS
New Orleans, Louisiana, United States, 70112-2699
United States, Maryland
IHV Baltimore Treatment CRS
Baltimore, Maryland, United States, 21201
Johns Hopkins University CRS
Baltimore, Maryland, United States, 21287
United States, Massachusetts
Beth Israel Deaconess Med. Ctr., ACTG CRS
Boston, Massachusetts, United States, 02215
Bmc Actg Crs
Boston, Massachusetts, United States, 02118
Boston Medical Center Ped. HIV Program NICHD CRS
Boston, Massachusetts, United States, 02118
Brigham and Women's Hospital Therapeutics Clinical Research Site (BWH TCRS) CRS
Boston, Massachusetts, United States, 02115
Massachusetts General Hospital CRS (MGH CRS)
Boston, Massachusetts, United States, 02114
United States, Michigan
Henry Ford Hosp. CRS
Detroit, Michigan, United States, 48202
Wayne State Univ. CRS
Detroit, Michigan, United States, 48201
United States, Missouri
Washington University Therapeutics (WT) CRS
St. Louis, Missouri, United States, 63110
United States, New Jersey
Cooper Univ. Hosp. CRS
Camden, New Jersey, United States, 08103
New Jersey Medical School Clinical Research Center CRS
Newark, New Jersey, United States, 07103
Rutgers - New Jersey Medical School CRS
Newark, New Jersey, United States, 07103
United States, New York
Bronx-Lebanon Hosp. Ctr. CRS
Bronx, New York, United States, 10457
Columbia IMPAACT CRS
New York, New York, United States, 10032
Harlem ACTG CRS
New York, New York, United States, 10037
NY Univ. HIV/AIDS CRS
New York, New York, United States, 10016
Nyu Ny Nichd Crs
New York, New York, United States, 10016
Metropolitan Hosp. NICHD CRS
New York, New York, United States, 10029
Weill Cornell Chelsea CRS
New York, New York, United States, 10011
Columbia P&S CRS
New York, New York, United States, 10032-3732
Univ. of Rochester ACTG CRS
Rochester, New York, United States, 14642
Trillium Health ACTG CRS
Rochester, New York, United States, 14607
United States, North Carolina
Chapel Hill CRS
Chapel Hill, North Carolina, United States, 27514
Duke Univ. Med. Ctr. Adult CRS
Durham, North Carolina, United States, 27710
United States, Ohio
Cincinnati CRS
Cincinnati, Ohio, United States, 45267-0405
Case CRS
Cleveland, Ohio, United States, 44106
MetroHealth CRS
Cleveland, Ohio, United States, 44109
Ohio State University CRS
Columbus, Ohio, United States, 43210
United States, Oregon
The Research & Education Group-Portland CRS
Portland, Oregon, United States, 97210
United States, Pennsylvania
Penn Therapeutics, CRS
Philadelphia, Pennsylvania, United States, 19104
Thomas Jefferson Univ. Med. Ctr. CRS
Philadelphia, Pennsylvania, United States, 19107
University of Pittsburgh CRS
Pittsburgh, Pennsylvania, United States, 15213-2582
United States, Rhode Island
The Miriam Hospital Clinical Research Site (TMH CRS) CRS
Providence, Rhode Island, United States, 02906
United States, Tennessee
St. Jude Children's Research Hospital CRS
Memphis, Tennessee, United States, 38105
Vanderbilt Therapeutics (VT) CRS
Nashville, Tennessee, United States, 37204
United States, Texas
Trinity Health and Wellness Center CRS
Dallas, Texas, United States, 75208
Houston AIDS Research Team CRS
Houston, Texas, United States, 77030
Texas Children's Hospital CRS
Houston, Texas, United States, 77030
United States, Virginia
Virginia Commonwealth Univ. Medical Ctr. CRS
Richmond, Virginia, United States, 23298
United States, Washington
University of Washington AIDS CRS
Seattle, Washington, United States, 98104
Puerto Rico
San Juan City Hosp. PR NICHD CRS
San Juan, Puerto Rico, 00936
Puerto Rico AIDS Clinical Trials Unit CRS
San Juan, Puerto Rico, 00935
University of Puerto Rico Pediatric HIV/AIDS Research Program CRS
San Juan, Puerto Rico, 00935
Sponsors and Collaborators
AIDS Clinical Trials Group
Investigators
Study Chair: Karen T. Tashima, MD Brown University
Study Chair: Richard H. Haubrich, MD Division of Infectious Diseases, UCSD Antiviral Research Center
  More Information

Additional Information:
Publications:
Responsible Party: National Institute of Allergy and Infectious Diseases (NIAID)
ClinicalTrials.gov Identifier: NCT00537394     History of Changes
Other Study ID Numbers: A5241, 10395, ACTG A5241, OPTIONS
Study First Received: September 27, 2007
Results First Received: June 14, 2013
Last Updated: July 14, 2014
Health Authority: United States: Food and Drug Administration

Keywords provided by National Institute of Allergy and Infectious Diseases (NIAID):
Treatment Experienced

Additional relevant MeSH terms:
HIV Infections
Acquired Immunodeficiency Syndrome
Lentivirus Infections
Retroviridae Infections
RNA Virus Infections
Virus Diseases
Sexually Transmitted Diseases, Viral
Sexually Transmitted Diseases
Immunologic Deficiency Syndromes
Immune System Diseases
Slow Virus Diseases
Enfuvirtide
Tipranavir
Darunavir
Etravirine
HIV Fusion Inhibitors
Molecular Mechanisms of Pharmacological Action
Pharmacologic Actions
Anti-HIV Agents
Anti-Retroviral Agents
Antiviral Agents
Anti-Infective Agents
Therapeutic Uses
Reverse Transcriptase Inhibitors
Nucleic Acid Synthesis Inhibitors
Enzyme Inhibitors
HIV Protease Inhibitors
Protease Inhibitors

ClinicalTrials.gov processed this record on August 28, 2014