An Open Label Demonstration Project and Phase II Safety Study of Pre-Exposure Prophylaxis Use Among 15 to 17 Year Old Young Men Who Have Sex With Men (YMSM)
- Conditions
- HIV Infection
- Interventions
- Behavioral: PCCDrug: Emtricitabine/tenofovir (FTC/TDF (Truvada®))
- Registration Number
- NCT01769456
- Lead Sponsor
- University of North Carolina, Chapel Hill
- Brief Summary
Approximately 100 HIV-uninfected YMSM at high risk of acquiring HIV infection, between the ages of 15 and 17 inclusive will be enrolled across all participating Adolescent Medicine Trial Units (AMTUs). Subjects will complete the behavioral intervention selected by all participating sites, Personalized Cognitive Counseling (PCC), and will then be provided with open label emtricitabine (FTC)/tenofovir (TDF) (Truvada®) as pre-exposure prophylaxis (PrEP). Behavioral and biomedical data will be collected at baseline and at 0, 4, 8, 12, 24, 36 and 48 weeks. Any subject who becomes HIV infected during the course of the study will be discontinued from the study agent and be followed for an additional 24 weeks after the study visit at which HIV infection is confirmed. Those subjects who meet specific bone or renal criteria at the Week 48 visit or the 24-Week HIV Seropositive visit will be followed for an additional 48 weeks in the Extension Phase to monitor longer-term outcomes of potential concerns.
- Detailed Description
The aims of the study are to obtain additional data on the safety of FTC/TDF (Truvada®) and to evaluate acceptability, patterns of use, rates of adherence, and measured levels of drug exposure when YMSM are provided with open label FTC/TDF (Truvada®) and information regarding safety and efficacy of FTC/TDF (Truvada®) as PrEP based on prior studies in adults. The study will also examine patterns of sexual risk behavior among HIV-uninfected YMSM in the U.S. at high risk of acquiring HIV infection who are provided with open label FTC/TDF (Truvada®) as PrEP. The study will also explore the feasibility and acceptability of implementing an efficacious risk reduction behavioral intervention prior to the provision of PrEP- PCC. The inclusion of a behavioral intervention in this project not only addresses the ethical responsibility of providing at least the minimum risk reduction education to all subjects given the high HIV risk of the study population, but also builds behavioral skills to assist subjects in reducing their risk when not taking PrEP. Furthermore, the study will evaluate the process of protocol implementation to better understand how to best implement PrEP research and program practice at adolescent medicine sites, including an evaluation of consent procedures and the acceptability/feasibility of allowing youth minors to consent for their own participation in HIV prevention intervention, to the extent allowable by local laws and regulations, and to allow youth minor participation in a clinical trial without requiring disclosure of their sexual orientation and risk behaviors to their parents or legal guardians.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Male
- Target Recruitment
- 78
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Willing and able to provide written informed consent;
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Male gender at birth;
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Age 15 years and 0 days through 17 years and 364 days, inclusive, at the time of signed informed consent;
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Self reports evidence of high risk for acquiring HIV infection including at least one of the following:
- At least one episode of unprotected anal intercourse with an HIV-infected male partner or a male partner of unknown HIV status during the last 6 months;
- Anal intercourse with 3 or more male sex partners during the last 6 months;
- Exchange of money, gifts, shelter, or drugs for anal sex with a male partner during the last 6 months;
- Sex with a male partner and has had a sexually transmitted infection (STI) during the last 6 months or at screening;
- Sexual partner of an HIV-infected man with whom condoms were not consistently used in the last 6 months; or
- At least one episode of anal intercourse where the condom broke or slipped off during the last 6 months;
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Tests HIV antibody negative at time of screening;
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Willing to provide locator information to study staff;
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Willing to take PrEP;
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Willing to participate in behavioral intervention;
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Reports intention not to relocate out of AMTU study area during the course of the study; and
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Does not have a job or other obligations that would require long absences from AMTU study area (greater than 4 weeks at a time).
- Appears visibly distraught or presence of active serious psychiatric symptoms (e.g., active hallucinations, suicidal, homicidal, or exhibiting violent behavior) at the time of consent;
- Intoxicated or under the influence of alcohol or other drugs at the time of consent;
- Any significant uncontrolled, active or chronic disease process that, in the judgment of the site investigator, would make participation in the study inappropriate. (Appropriately managed conditions, like well-controlled diabetes, would not preclude enrollment; the site is encouraged to contact the Adolescent Medicine Trials Network for HIV/AIDS Interventions (ATN) 113 Protocol Team if they are having difficulty making the judgment.);
- History of bone fractures not explained by trauma;
- Acute or chronic hepatitis B infection as indicated by positive hepatitis B surface antigen (sAg) test at time of screening;
- Confirmed renal dysfunction (Creatinine Clearance (CrCl) < 75 ml/min calculated based on bedside Schwartz formula: Glomerular filtration rate (GFR) = (0.413 x (height in centimeters)) / (serum creatinine in mg/dl)), or serum creatinine > upper limit of normal (ULN), or history of renal parenchymal disease or presence of only one kidney at time of screening;
- Confirmed ≥ Grade 2 hypophosphatemia at time of screening;
- Confirmed ≥ Grade 2 hematologic system abnormality (White Blood Count (WBC), Absolute Neutrophil Count (ANC), hemoglobin, or platelets) at time of screening;
- Confirmed ≥ Grade 2 hepatobiliary system abnormality (Aspartate aminotransferase (AST), Alanine aminotransferase (ALT), or bilirubin) at time of screening;
- Confirmed proteinuria as indicated by urine dipstick result ≥ 1+ at time of screening, regardless of urine protein to creatinine ratio (UP/C);
- UP/C > 0.37 g/g at time of screening, regardless of urine dipstick protein result;
- Confirmed normoglycemic glucosuria as indicated by urine dipstick result ≥ 1+ in the presence of normal serum glucose (<120 mg/dL) at time of screening;
- A confirmed Grade ≥ 3 toxicity on any screening evaluations;
- Known allergy/sensitivity to the study agent or its components;
- Concurrent participation in an HIV vaccine study or other investigational drug study, including oral or topical PrEP (microbicide) studies;
- Use of disallowed medications; or
- Inability to understand spoken English.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description PCC Behavioral Intervention Group PCC PCC Behavioral Intervention combined with open label FTC/TDF (Truvada®) as PrEP PCC Behavioral Intervention Group Emtricitabine/tenofovir (FTC/TDF (Truvada®)) PCC Behavioral Intervention combined with open label FTC/TDF (Truvada®) as PrEP
- Primary Outcome Measures
Name Time Method Number of Participants With Decrease in Bone Mineral Density 48 weeks The proportion of subjects with DXA data through Week 48 who experienced varying degrees of decrease in absolute BMD in at least one region (spine, hip, or whole body).
This represents one of the indicators associated with the objective: Additional safety data regarding FTC/TDF (Truvada®) use among HIV-uninfected YMSM.Lumbar Spine Bone Mineral Density: Percent Change From Baseline to Week 48 Baseline, Week 48 The percent change in lumbar spine BMD from baseline measurement to Week 48 is calculated as:
Percent change= \[(Value at Week 48 - Value at Baseline)/(Value at Baseline)\] x 100
This represents one of the indicators associated with the objective: Additional safety data regarding FTC/TDF (Truvada®) use among HIV-uninfected YMSM.Femoral Neck Bone Mineral Density: Percent Change From Baseline to Week 48 Baseline, Week 48 The percent change in femoral neck BMD from baseline measurement to Week 48 is calculated as:
Percent change= \[(Value at Week 48 - Value at Baseline)/(Value at Baseline)\] x 100
This represents one of the indicators associated with the objective: Additional safety data regarding FTC/TDF (Truvada®) use among HIV-uninfected YMSM.Total Body Bone Mineral Density: Percent Change From Baseline to Week 48 Baseline, Week 48 The percent change in total body BMD from baseline measurement to Week 48 is calculated as:
Percent change= \[(Value at Week 48 - Value at Baseline)/(Value at Baseline)\] x 100
This represents one of the indicators associated with the objective: Additional safety data regarding FTC/TDF (Truvada®) use among HIV-uninfected YMSM.Total Hip Bone Mineral Density: Percent Change From Baseline to Week 48 Baseline, Week 48 The percent change in total hip BMD from baseline measurement to Week 48 is calculated as:
Percent change= \[(Value at Week 48 - Value at Baseline)/(Value at Baseline)\] x 100
This represents one of the indicators associated with the objective: Additional safety data regarding FTC/TDF (Truvada®) use among HIV-uninfected YMSM.Behavioral Disinhibition/Risk Compensation: Number of Participants Reporting Unprotected Sex Week 48 Behavioral disinhibition/risk compensation was assessed based on a number of questions, including the following related to unprotected sex from the participant ACASI:
"Of these males \[male partners\], how many did you have unprotected oral or anal sex with since the last time you took this survey?" An event is defined as an answer of greater than 0.
This represents one of the indicators associated with the objective: Additional safety data regarding FTC/TDF (Truvada®) use among HIV-uninfected YMSM.Number of Participants With Serum Creatinine Event of Grade 1 or Higher Over the Course of the Study 48 weeks This represents one of the indicators associated with the objective: Additional safety data regarding FTC/TDF (Truvada®) use among HIV-uninfected YMSM.
Participants were assessed for any serum creatinine event of Grade 1 or higher over the course of the study (Week 0 through Week 48).Behavioral Disinhibition/Risk Compensation: Number of Male Sexual Partners Week 48 Behavioral disinhibition/risk compensation was assessed based on a number of questions, including the following related to related to number of male sexual partners from the participant ACASI:
"Since the last time you took this survey, how many male partners have you had sexual contact with (oral or anal)?"
This represents one of the indicators associated with the objective: Additional safety data regarding FTC/TDF (Truvada®) use among HIV-uninfected YMSM.Acceptability of PrEP Regimen and Study Visits Week 12 This represents one of the indicators associated with the objective: Acceptability when YMSM are provided open label FTC/TDF (Truvada®) and information regarding the safety and efficacy of PrEP from prior studies.
Acceptability of PrEP as measured by the acceptability assessment that includes questions on usability of PrEP, user-friendliness of the medication regimen, including an assessment of side effects and delivery format, and acceptability of behavioral intervention sessions.Estimation of Medication Adherence by Dried Blood Spot (DBS) Results Week 4, Week 12, Week 24, Week 36, Week 48 This outcome addresses the objective: Rates of adherence and measured levels of drug exposure when YMSM are provided open label FTC/TDF (Truvada®) and information regarding the safety and efficacy of PrEP from prior studies.
Medication adherence is estimated by factors including levels of drug exposure as measured by DBS red blood cell (RBC) samples.
The TFV dosing level was translated into number of dosing days per week for week 8 onwards using lab estimates as follows: '\<2 days' is defined as \<350 (fmol/punch), '2 days' as 350 to 700 (fmol/punch), '4 days' as \>700 to 1250 (fmol/punch), and 'Daily' as \>1250 (fmol/punch).
The TFV dosing level was translated into number of dosing days for week 4 using lab estimates as follows: '\<2 days' is defined as \<275 (fmol/punch), '2 days' as 275 to 525 (fmol/punch), '4 days' as \>525 to 950 (fmol/punch),and 'Daily' as \>950 (fmol/punch)
- Secondary Outcome Measures
Name Time Method Number of Participants Using Text Messaging Reminders Baseline through Week 48 This represents one of the indicators associated with the objective: Acceptability and feasibility of text message reminders.
Acceptability and Feasibility of Two Types of Efficacious Sexual Risk Reduction Interventions as Measured by Session Evaluation 48 weeks Study subjects were given a brief Session Evaluation Form at the end of the behavioral intervention session consisting of ten items on a 4-point response scale aimed at eliciting information about the subject's experience with the session (i.e., was session interesting, was it relevant to their life, and did they learn from the session)
Rating of the Reasons for Missing Medications on a 4-point Likert Scale. 48 weeks This represents one of the indicators associated with the objective: Acceptability and feasibility of text message reminders, as measured by subject rating of the reasons for missing medications on a 4-point Likert scale.
Subjects were asked to rate various measures as "Never," "Rarely," "Sometimes," or "Often" the reason for missing taking study pills. Data shown for Week 48.
Question: In the past month, how often have you missed taking your study pills because you:Demographic and/or Behavioral Difference Between Study Groups. Behavioral Disinhibition/Risk Compensation Endpoints Will be Compared. 48 weeks Evaluation of the Process of Protocol Implementation 48 weeks Brief phone interviews and review of written institutional review board (IRB) correspondence will be conducted for all sites whether the study is approved at that site or not. If approved, the steps needed for approval and how barriers were addressed will be examined. If the study was rejected, the reasons for disapproval, the IRB's interpretation of the risk of PrEP, and other barriers will be examined. In addition, data from a survey specific to each site's IRB's responses of minor YMSM inclusion in PrEP studies will be evaluated.
NOTE: Data collected to address this outcome were primarily qualitative in nature, and as such are not presented here. For more information on this outcome, refer to:
Gilbert AL, Knopf AS, Fortenberry JD, Hosek SG, Kapogiannis BG, Zimet GD. Adolescent Self-Consent for Biomedical Human Immunodeficiency Virus Prevention Research. J Adolesc Health. 2015 Jul;57(1):113-9.Demographic and/or Behavioral Differences Between Youth Who Are Interested in Participating in a PrEP Study Versus Those Who Are Not. 48 weeks Behavioral disinhibition/risk compensation endpoints will be compared.
Trial Locations
- Locations (6)
Childrens Hospital of Philadelphia
🇺🇸Philadelphia, Pennsylvania, United States
Stroger Hospital of Cook County
🇺🇸Chicago, Illinois, United States
Fenway Institute
🇺🇸Boston, Massachusetts, United States
Children's Hospital of Los Angeles
🇺🇸Los Angeles, California, United States
Tulane Medical Center
🇺🇸New Orleans, Louisiana, United States
University of Colorado - The Children's Hospital of Denver
🇺🇸Aurora, Colorado, United States