Collection of Samples From HIV-1 Infected Individuals for Evaluation of the Aptima HIV-1 Assay

This study is currently recruiting participants. (see Contacts and Locations)
Verified July 2014 by Gen-Probe, Incorporated
Sponsor:
Information provided by (Responsible Party):
Gen-Probe, Incorporated
ClinicalTrials.gov Identifier:
NCT02026752
First received: December 31, 2013
Last updated: July 11, 2014
Last verified: July 2014
  Purpose

The objective is to obtain plasma samples from Human Immunodeficiency Virus Type 1 (HIV-1) infected individuals that have viral loads across the dynamic range of the Aptima HIV-1 assay. The plasma samples will be tested in a method comparison study to support the approval of the Aptima HIV-1 assay on Gen-Probe's Panther testing system. The objective of the method comparison study is to evaluate the clinical utility of the Aptima HIV-1 assay by comparing the results to the FDA-licensed COBAS assay (Roche Molecular Systems, Inc., Branchburg, New Jersey) in plasma samples that have viral loads across the dynamic range of the Aptima HIV-1 assay.


Condition
HIV-1 Infection

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Cross-Sectional
Official Title: Collection of Plasma Samples From Human Immunodeficiency Virus (HIV) Type 1 (HIV-1) Infected Individuals for the Clinical Evaluation of the Aptima HIV-1 Quant Dx Assay

Resource links provided by NLM:


Further study details as provided by Gen-Probe, Incorporated:

Primary Outcome Measures:
  • Quantitative detection of HIV-1 RNA [ Time Frame: single baseline visit ] [ Designated as safety issue: No ]
    Regression parameters (intercept and slope) will be estimated from method comparison analysis.


Biospecimen Retention:   Samples With DNA

plasma


Estimated Enrollment: 1200
Study Start Date: January 2014
Estimated Primary Completion Date: February 2015 (Final data collection date for primary outcome measure)
Groups/Cohorts
Study Population

  Eligibility

Ages Eligible for Study:   15 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

HIV-infected male and female subjects ≥15 years of age who are attending participating US medical facilities will be eligible to enroll. Participating sites may include academic institutions with clinical divisions, infectious disease clinics, and other medical facilities such as sexually transmitted infection, HIV, and public health facilities

Criteria

Inclusion Criteria

  • The subject has documented HIV infection
  • The subject is at least 15 years of age at the time of enrollment
  • For ART subjects, subject has documented HIV-1 RNA levels above the lower limit of quantitation of an FDA-approved assay in a sample collected in the past 90 days.
  • The subject (and/or legally authorized representative, if allowed) is willing and able to provide written informed consent before providing a specimen (a minor will need the documented consent of his/her parent or legal guardian, unless the site has an institutional review board [IRB]-approved waiver for parental consent for minors).

Exclusion Criteria

  • A potential subject will be ineligible for the study if the subject, clinician, or medical record reports any of the following:
  • Subject's HIV disease stage and/or current ART status is unknown.
  • It is unknown if current or previous ART was changed or stopped due to therapy failure.
  • For non-ART subjects, subject was previously on ART in the past 30 days
  • Subject already participated in this study and subject's previous sample(s) was provided and not withdrawn (ie, subject has an evaluable sample in the study)
  • Subject has a history of illness that the principal investigator (PI) or designee considers could interfere with or affect the conduct, results, and/or completion of the study
  • Subject has a history of illness that the PI or designee considers could create an unacceptable risk to the subject if enrolled in the study
  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: NCT02026752

Locations
United States, California
Palmtree Clinical Research Inc Recruiting
Palm Springs, California, United States, 92262
Contact: Erik Hernandez    760-778-7799      
Principal Investigator: Richard Loftus, MD         
UCSD - AnitViral Research Center (AVRC) Recruiting
San Diego, California, United States, 92103
Contact: Sanjay Mehta, MD    858-822-4092    srmehta@ucsd.edu   
Principal Investigator: Sanjay Mehta, MD         
United States, Connecticut
Yale University Recruiting
New Haven, Connecticut, United States, 06510
Contact: Michael Kozal, MD    203-737-4040    michael.kozal@yale.edu   
Principal Investigator: Michael Kozal, MD         
United States, Florida
University of Miami - AIDS Clinical Research Unit Recruiting
Miami, Florida, United States, 33136
Contact: Margaret Fischl, MD    305-243-8125    m.fischl@miami.edu   
Principal Investigator: Margaret Fischl, MD         
Community AIDS Network Recruiting
Sarasota, Florida, United States, 34237
Contact: Mig Entcheva, MD    941-366-0134      
Principal Investigator: Tanya Schreibman, MD         
United States, Indiana
Wishard Health Services Recruiting
Indianapolis, Indiana, United States, 46202
Contact: Thomas Davis, MD    317-274-3391    ThDavis@iupui.edu   
Principal Investigator: Thomas Davis, MD         
United States, Louisiana
Louisiana State University Not yet recruiting
New Orleans, Louisiana, United States, 70112
Contact: Stephanie Taylor, MD    504-568-4132    staylo2@lsuhsc.edu   
Principal Investigator: Stephanie Taylor, MD         
United States, Maryland
Johns Hopkins University Not yet recruiting
Baltimore, Maryland, United States, 21287
Contact: Timothy Amukele, MD    410-502-5296    tamukele@jhmi.edu   
Principal Investigator: Timothy Amukele, MD         
United States, New York
Jacobi Medical Center Recruiting
Bronx, New York, United States, 10461
Contact: Jason Leider, MD    718-918-3669    Jason.Leider@NBHN.net   
Principal Investigator: Jason Leider, MD         
Sponsors and Collaborators
Gen-Probe, Incorporated
Investigators
Study Director: Jennifer L Reid, PhD Hologic Gen-Probe
  More Information

No publications provided

Responsible Party: Gen-Probe, Incorporated
ClinicalTrials.gov Identifier: NCT02026752     History of Changes
Other Study ID Numbers: HIVQPS-US12-001, HIVQPS-US12-002, HIVQPS-US12-003, HIVQPS-US12-004
Study First Received: December 31, 2013
Last Updated: July 11, 2014
Health Authority: United States: Institutional Review Board

Additional relevant MeSH terms:
Acquired Immunodeficiency Syndrome
HIV Infections
Lentivirus Infections
Retroviridae Infections
RNA Virus Infections
Virus Diseases
Sexually Transmitted Diseases, Viral
Sexually Transmitted Diseases
Slow Virus Diseases
Immunologic Deficiency Syndromes
Immune System Diseases

ClinicalTrials.gov processed this record on September 16, 2014