Seroincidence Study Among Men Who Have Sex With Men and Transgender Women - The ImPrEP Seroincidence Study

Sponsor
Evandro Chagas National Institute of Infectious Disease (Other)
Overall Status
Completed
CT.gov ID
NCT05674682
Collaborator
Valdiléa Veloso dos Santos, Ph.D. (Other), Beatriz Grinzstejn, MD, PhD (Other), Brenda Hoagland, MD, PhD (Other), Celia Landmann Szwarcwald, PhD (Other), Thiago Torres, PhD (Other), Maria Cristina Pimenta, MD, PhD (Other), Marcos Benedetti, MA (Other), Marília Santini Oliveira (Other), Ronaldo Ismério Moreira, PhD (Other), Sandro Nazer Coutinho (Other), Sylvia Lopes Maia Teixeira, PhD (Other), Nilo Martínez Fernandes, PhD (Other), Hamid Vega-Ramírez, MD, MSc (Other), Sérgio Bautista-Arredondo, MD, PhD (Other), René Leyva-Flores, PhD (Other), Helleen Vermandere (Other), Santiago Ávila-Ríos, PhD (Other), Claudia García-Morales, PhD (Other), Carlos Cáceres, MD, MPH, PhD (Other), Kelika A. Konda, PhD (Other), Juan Vicente Guanira, MD, PhD (Other), Giovanni Ravasi, MD, MScPH (Other)
4,000
2
1
9
2000
223

Study Details

Study Description

Brief Summary

PrEP (pre-exposure prophylaxis) is an effective prevention strategy in which HIV-negative individuals take antiretroviral drugs (tenofovir disoproxil fumarate and emtricitabine - TDF/FTC) to reduce HIV acquisition. Clinical studies have shown that the TDF/FTC combination protects MSM and transgender women against HIV infection. According to the PROUD study, PrEP can decrease the risk of HIV infection among MSM by 86% (90% CI 64-96). The international community recognizes that PrEP can be an additional tool in the framework of a combination prevention package for those most at risk of contracting HIV. Data on HIV incidence among MSM and trans women are largely unknown. In Brazil, Mexico and Peru, data on the incidence of HIV among MSM and trans women are very scarce, limited to small cross-sectional studies.Current methods used to determine HIV-1 incidence have many limitations. These methods include mathematical modeling, retrospective calculations of AIDS case reports, age-based prevalence determinations, and prevalence determinations with multiple rounds of longitudinal surveys to estimate HIV incidence, which require numerous assumptions and inputs and can pose additional challenges in the era of expansion of antiretroviral therapy (ART) and increased survival of HIV-1 infected individuals. On the other hand, prospective longitudinal cohort studies of high-risk individuals can be used to estimate incidence; however, they are often labor-intensive, complex, very expensive, difficult to implement in most countries, and have recruitment biases. Laboratory methods can be unbiased and do not require complicated assumptions and case-by-case weighting. The cross-sectional use of Recent HIV Infection Tests (TRIs) based on biomarkers offers, in principle, accessible, reliable and low risk of bias options for estimating incidence.

Condition or Disease Intervention/Treatment Phase
  • Procedure: HIV testing
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
4000 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
MSM and TGW, aged 18 yo or moreMSM and TGW, aged 18 yo or more
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Seroincidence Study Among Men Who Have Sex With Men and Transgender Women - The ImPrEP Seroincidence Study. A Sub-study of Implementation of HIV Pre-exposure Prophylaxis (PrEP) for Men Who Have Sex With Men and Transgender People: A Demonstration Project in the Context of Combined Prevention in Brazil, Mexico and Peru - the ImPrEP Study
Actual Study Start Date :
Oct 1, 2019
Actual Primary Completion Date :
May 31, 2020
Actual Study Completion Date :
Jun 30, 2020

Arms and Interventions

Arm Intervention/Treatment
Other: Venipuncture or digital puncture for HIV test

MSM and transgender women aged 18 years or older, willing and able to sign informed consent to accept venipuncture or digital puncture for HIV testing

Procedure: HIV testing
venipuncture or digital puncture for HIV testing

Outcome Measures

Primary Outcome Measures

  1. Identification of recent infections in a given high-risk population (MSM and TGW), including those in defined geographic areas for evaluate epidemics, calibrate models, design and evaluate interventions. [2 years]

    Blood collected for viral load from those with confirmed HIV infection will be used to distinguish recent HIV-1 infections of long-term infections

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • MSM and transgender women

  • aged 18 years or older

  • willingness and ability to sign an informed consent form.

Exclusion Criteria:
  • Individuals currently using PrEP, PEP or receiving antiretroviral therapy;

  • Individuals unable to understand the study or who do not agree to sign the consent form;

  • Individuals who are participating in a clinical trial of antiretroviral medication or any investigational product to prevent the acquisition of HIV infection (for example, monoclonal antibodies such as PEP or PrEP)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Instituto Nacional de Infectologia Evandro Chagas (Fiocruz) Rio de Janeiro RJ Brazil 21040-360
2 Instituto Nacional de Infectologia Evandro Chagas/ FIOCRUZ Rio De Janeiro Brazil 21040-360

Sponsors and Collaborators

  • Evandro Chagas National Institute of Infectious Disease
  • Valdiléa Veloso dos Santos, Ph.D.
  • Beatriz Grinzstejn, MD, PhD
  • Brenda Hoagland, MD, PhD
  • Celia Landmann Szwarcwald, PhD
  • Thiago Torres, PhD
  • Maria Cristina Pimenta, MD, PhD
  • Marcos Benedetti, MA
  • Marília Santini Oliveira
  • Ronaldo Ismério Moreira, PhD
  • Sandro Nazer Coutinho
  • Sylvia Lopes Maia Teixeira, PhD
  • Nilo Martínez Fernandes, PhD
  • Hamid Vega-Ramírez, MD, MSc
  • Sérgio Bautista-Arredondo, MD, PhD
  • René Leyva-Flores, PhD
  • Helleen Vermandere
  • Santiago Ávila-Ríos, PhD
  • Claudia García-Morales, PhD
  • Carlos Cáceres, MD, MPH, PhD
  • Kelika A. Konda, PhD
  • Juan Vicente Guanira, MD, PhD
  • Giovanni Ravasi, MD, MScPH

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Raquel Malaguthi de Souza, Regulatory Affairs Associate, Evandro Chagas National Institute of Infectious Disease
ClinicalTrials.gov Identifier:
NCT05674682
Other Study ID Numbers:
  • 20012619.9.1001.5262
First Posted:
Jan 6, 2023
Last Update Posted:
Jan 6, 2023
Last Verified:
Jan 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by Raquel Malaguthi de Souza, Regulatory Affairs Associate, Evandro Chagas National Institute of Infectious Disease
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 6, 2023