Patient progress through enrollment, follow-up, and analysis. HIV indicates human immunodeficiency virus; AMTU, adolescent medicine trial unit; PCC, personalized cognitive counseling.
aSome screening data were lost at 1 site and are not included.
bThe received PPC category represents the number of participants who received the PCC intervention.
BLQ indicates below the lower limit of quantitation.
TFV indicates tenofovir diphosphate.
eTable. Sexual Risk Behaviors by Study Visit—Median and Interquartile Range
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Hosek SG, Landovitz RJ, Kapogiannis B, et al. Safety and Feasibility of Antiretroviral Preexposure Prophylaxis for Adolescent Men Who Have Sex With Men Aged 15 to 17 Years in the United States. JAMA Pediatr. 2017;171(11):1063–1071. doi:10.1001/jamapediatrics.2017.2007
Is human immunodeficiency virus preexposure prophylaxis safe and feasible to use for adolescent men who sex with men?
In this study, preexposure prophylaxis was found to be safe and well-tolerated, but adherence to the daily pill waned. Rates of sexually transmitted infections were high and human immunodeficiency virus infections occurred among those with poor adherence.
Adolescent men who have sex with men who are at risk of contracting the human immunodeficiency virus should be offered access to preexposure prophylaxis with appropriate behavioral support to maintain adherence.
Adolescents represent a key population for implementing preexposure prophylaxis (PrEP) interventions worldwide, yet tenofovir disoproxil fumarate/emtricitabine (TDF/FTC) for PrEP is only licensed for adults.
To examine the safety of and adherence to PrEP along with changes in sexual risk behavior among adolescent men who have sex with men (MSM).
Design, Setting, and Participants
Adolescent Medicine Trials Network for HIV/AIDS Interventions 113 (Project PrEPare) was a PrEP demonstration project that evaluated the safety, tolerability, and acceptability of TDF/FTC and patterns of use, rates of adherence, and patterns of sexual risk behavior among healthy young MSM aged 15 to 17 years. Participants were recruited from adolescent medicine clinics and their community partners in 6 US cities, had negative test results for human immunodeficiency virus (HIV) but were at high risk for acquiring an infection, and were willing to participate in a behavioral intervention and accept TDF/FTC as PrEP.
All participants completed an individualized evidence-based behavioral intervention and were provided with daily TDF/FTC as PrEP for 48 weeks.
Main Outcomes and Measures
The main objectives were to: (1) provide additional safety data regarding TDF/FTC use among young MSM who had negative test results for HIV; (2) examine the acceptability, patterns of use, rates of adherence, and measured levels of tenofovir diphosphate in dried blood spots; and (3) examine patterns of risk behavior when young MSM were provided with a behavioral intervention in conjunction with open-label TDF/FTC.
Among 2864 individuals screened (from August 2013 to September 2014), 260 were eligible and 78 were enrolled (mean [SD] age, 16.5 [0.73] years), of whom 2 (3%) were Asian/Pacific Islander, 23 (29%) were black/African American, 11 (14%) were white, 16 (21%) were white Hispanic, and 26 (33%) were other/mixed race/ethnicity. Over 48 weeks of PrEP use, 23 sexually transmitted infections were diagnosed in 12 participants. The HIV seroconversion rate was 6.4 (95% CI: 1.3-18.7) per 100 person-years. Tenofovir diphosphate levels consistent with a high degree of anti-HIV protection (>700 fmol/punch) were found in 42 (54%), 37 (47%), 38 (49%), 22 (28%), 13 (17%), and 17 (22%) participants at weeks 4, 8, 12, 24, 36, and 48, respectively.
Conclusions and Relevance
Adolescent Medicine Trials Network for HIV/AIDS Interventions 113 enrolled a diverse sample of adolescent MSM at risk for HIV who consented to study participation. Approximately half achieved protective drug levels during the monthly visits, but adherence decreased with quarterly visits. Youth may need additional contact with clinical staff members to maintain high adherence.
clinicaltrials.gov Identifier: NCT01769456
In July 2012, the US Food and Drug Administration approved the use of tenofovir disoproxil fumarate/emtricitabine (TDF/FTC) for human immunodeficiency virus (HIV) preexposure prophylaxis (PrEP) based on 3 studies that demonstrated efficacy for preventing HIV.1-3 Since then, several open-label clinical trials and demonstration projects have supported the effectiveness of administering daily oral PrEP to prevent HIV.4-7 None of these clinical trials included adolescent participants younger than 18 years, precluding regulatory agencies from considering the approval of TDF/FTC use for minors. Thus, a critical gap in approved prevention products exists for adolescents, a population that is highly vulnerable to HIV worldwide.
According to the World Health Organization,8 AIDS is the leading cause of death among adolescents in sub-Saharan Africa and the second leading cause for adolescents worldwide. In 2015, there were an estimated 1.8 million adolescents aged 10 to 19 years who were living with HIV, and an adolescent aged 10 to 19 years was infected with HIV every 2 minutes.9 In the United States, adolescents and young adults aged 13 to 24 years made up 22% of all new infections in 2014, and 80% of those infections were among young men who have sex with men (YMSM).10
To expand regulatory approvals and inform PrEP implementation efforts for young people, we designed Adolescent Medicine Trials Network for HIV/AIDS Interventions113 (ATN 113) as an open-label demonstration project and phase 2 safety study for adolescent MSM age 15 to 17 years in the United States.
Participants were recruited in person and online through clinical sites that were affiliated with ATN. Eligible participants were aged 15 to 17 years, born male, and had negative test results for HIV as determined by a blood-based antibody assay and an HIV RNA assay at the screening visit. An additional requirement, based on similar criteria from the Preexposure Prophylaxis Initiative open-label trial,4 was self-reported risk for HIV acquisition via any of the following in the last 6 months: condomless anal intercourse with a male partner with an HIV infection or unknown HIV status, anal intercourse with at least 3 male partners, exchange sex, or sexually transmitted infection (STI). We excluded participants who had an estimated glomerular filtration rate of less than 75 mL/min using the bedside calculation by Schwartz and colleagues,11 and we also excluded those with a reactive hepatitis B surface antigen, a history of bone fractures, confirmed baseline hypophosphatemia, proteinuria or glycosuria, and liver function and hematology abnormalities that were grade 3 or more.
Eligible participants received 1 individual behavioral risk reduction session using Personalized Cognitive Counseling12 before the PrEP medication initiation. Study visits were conducted at baseline and monthly for 3 months, then quarterly through week 48. Participants received a comprehensive HIV prevention package that included regular HIV testing, sexual health and adherence promotion using Integrated Next Step Counseling,13 STI testing, and safety assessments at all visits. At each study visit, participants also completed behavioral assessments via an audio computer-assisted self-interview, received condoms, and were given the study drug.
The protocol was approved by the institutional review boards at all participating sites (Supplement 1). Adolescents were allowed to consent to study participation without parental consent and all participants provided written informed consent before undergoing any study procedures. A description of the process to allow adolescent consent has been described elsewhere.14,15 Participants were provided compensation for each study visit as determined by each site (range, $50-$75).
Assessments of acceptability were conducted at the 12- and 48-week visits using a questionnaire previously used with youth (eg, “How much did you like or not like taking a pill every day?”).16 Beliefs about PrEP were assessed using questions adapted from the Preexposure Prophylaxis Initiative open-label extension4 study to explore how PrEP may influence the health of participants, condom use, and sexual behavior, as well as reasons that participants would choose not to take PrEP (eg, “If I took PrEP, I would worry it was hurting my health”).
The AIDS Clinical Trials Group Adherence Follow-up Questionnaire17 was adapted to examine the possible reasons for missing PrEP doses and how often doses were missed for those reasons over the past month. Preexposure prophylaxis medication levels were assessed on dried blood spots collected at each visit to quantify intracellular tenofovir diphosphate (TFV-DP) and emtricitabine triphosphate (FTC-TP) concentrations in red blood cells.18 Results were translated into the dosing categories that were previously used in PrEP randomized clinical trials with adult MSM.4 Dosing categories included a below lower limit of quantitation, a lower limit of quantitation to 349 fmol per punch (fewer than 2 tablets per week), 350 to 699 fmol per punch (2-3 tablets per week), and 700 or more fmol per punch (4 or more tablets per week).
A self-report questionnaire was used to assess each participant’s general sexual history, as well as detailed sexual behavior with last partner. Participants were tested for syphilis at baseline and week 48, and as clinically indicated at other visits. Rectal swabs for nucleic acid amplification testing for gonorrhea (GC) and chlamydia (CT) were collected and assayed at baseline, 24 weeks, 48 weeks, and as clinically indicated at other visits. Urine-based nucleic acid amplification testing for GC and CT occurred at every visit. An STI was considered present based on a positive test result for urethral or rectal GC or CT or serologic evidence of syphilis (adjudicated based on current and prior rapid plasma reagin titers and history).
The investigative team monitored the study for clinical adverse events and abnormal laboratory values using the ATN Table for Grading Severity of Adolescent Adverse Events (October 2006–March 2011). Renal safety was monitored by measuring serum creatinine, dipstick urine protein, and glucose levels at each study visit. Bone mineral density (BMD) levels were measured by dual-energy radiography absorptiometry in the hip, spine, and total body at baseline, 24 weeks, and 48 weeks. An external data and safety monitoring board reviewed study safety data at 6-month intervals while the trial was being conducted and uniformly recommended that the study be completed.
The demographic and risk characteristics of the study population at baseline were examined using simple descriptive statistics. Categorical-scaled variables were described using frequencies and percentages, while continuous variables were examined in terms of medians and interquartile ranges (IQR). Some exploratory analyses were conducted. For example, bivariable relationships between study outcomes and characteristics of interest were examined using the Fisher exact test for categorical characteristics and the nonparametric Wilcoxon rank sum test for continuous characteristics when based on comparisons between independent groups. The McNemar test was used when comparing binary measures between time points among participants or using a generalized estimating equations approach for repeated measures to account for correlations among participants; an exchangeable (compound symmetry) correlation structure was assumed. The nonparametric Wilcoxon signed rank test was used to assess changes in continuous measures between time points among participants.
Cumulative STI incidence rates (and 95% CIs) were estimated separately for the 0- to 24- and 24- to 48-week period using a repeated-measures Poisson regression model; an unstructured correlation was specified in the models. In addition to yielding model-based estimates of the STI incidence rates, this approach also provided a statistical assessment that compared the rates between the study periods. Statistical significance was set at P = .05. All analyses were conducted using SAS, version 9.4 (SAS Institute).
Between August 2013 and September 2014, 78 participants enrolled in the study (Figure 1). Their mean (SD) age was 16.5 (0.73) years, and 23 (29%) self-identified as black/African American, 16 (21%) as white Hispanic, and 26 (33%) as other/mixed race/ethnicity. Most identified as gay (n = 45, 58%) or bisexual (n = 22, 28%). Most (n = 69, 88%) lived with their families and were currently in school (n = 67, 86%). In the month before baseline, 49 participants (67%) reported that they drank alcohol and 47 (64%) reported smoking marijuana. Twelve participants (15%) had been expelled from their homes because of their sexual orientation at some point, and 13 (17%) reported having exchanged sex for money. Twenty-four participants (60%) reported having condomless receptive anal intercourse with their last sexual partner, and 12 (15%) had a prevalent STI at study entry (Table 1).
Five participants failed to complete the week 0 visit within 30 days of screening and were prematurely discontinued from the study. Seventy-two participants (92%) began daily oral TDF/FTC and 46 (64%) of these completed 48 weeks of follow-up. Reasons for noncompletion are shown in Figure 1. Eight participants remained in study follow-up but chose to discontinue TDF/FTC.
Tenofovir disoproxil fumarate/emtricitabine was well tolerated overall and there were no confirmed laboratory abnormalities assessed as related to the study product. One participant permanently discontinued TDF/FTC because of grade 3 weight loss, which was assessed as possibly related to the study product. There were no renal events, elevations in serum creatinine levels, or bone fractures. Reasons for grade 3 or higher adverse events regardless of relations to the study product are shown in Table 2.
Dual-energy radiography absorptiometry scanning was performed in 75 participants. The mean baseline BMD was in the normal range for age, based on z scores (standard deviations adjusted for race/ethnicity and age and median −0.1, −0.1, and −0.2 in the spine, hip, and total body, respectively). At 48 weeks, results were available for 43 participants, for whom there were statistically significant increases from baseline in BMD in the spine (median 2.6%; IQR, 0.0-4.6; P < .001), hip (1.2%; IQR, −0.9 to 4.3; P = .02), and total body (0.7%; IQR, −0.2 to 2.6; P < .001). z Scores in the hip and spine did not change significantly from baseline to 48 weeks, but the total body BMD z score decreased (−0.20; IQR, −0.3 to 0.0; P < .001). Exploratory subgroup analyses revealed no statistically significant differences in change in BMD between participants with 48-week dried blood spot TFV-DP levels commensurate with 4 or more doses per week (>700 fmol/punch; n = 10), when compared with changes in those with levels associated with fewer than 2 doses per week (<350 fmol/punch; n = 24), or those with no evidence of recent dosing (below lower limit of quantification; n = 17).
At baseline, study participants reported a median of 1.0 (IQR, 1-3) male sexual partners in the past month. Numbers of sexual partners and condomless sex acts did not change significantly over time (eTable in the Supplement 2). Before PrEP initiation, 19 prevalent STIs were diagnosed in 14 participants (5 rectal GC, 8 rectal CT, 4 urine CT, and 2 syphilis). Over 48 weeks of PrEP use, 23 STIs were diagnosed in 12 participants (6 rectal GC, 8 rectal CT, 5 urine CT, 3 urine GC, and 1 syphilis). Sexually transmitted infection incidence rates that were estimated based on a Poisson regression model were higher in the first 24 weeks of the study (18.1/100 person-years; 95% CI, 9.7-34.0) compared with weeks 24 to 48 of the study (9.4/100 person-years; 95% CI, 3.4-25.6), but not significantly so (rate ratio, 1.93; 95% CI, 0.62-5.96; P = .25).
Adherence as measured by TFV-DP is depicted in Figure 2. Most participants had detectable drug levels throughout the study period, with more than 95% of participants having detectable levels over the first 12 weeks of treatment with declining levels thereafter. Among the 72 participants who were prescribed PrEP at the 0-week visit and who continued to participate in the study, levels of TFV-DP that were associated with high levels of protection against rectal HIV exposure (ie, consistent with taking a mean of 4 pills or more per week [>700 fmol/punch]) were found in 42 (54%), 37 (47%), 38 (49%), 22 (28%), 13 (17%), and 17 (22%) participants at weeks 4, 8, 12, 24, 36, and 48, respectively. Based on generalized estimating equations modeling, there were no statistically significant associations between condomless sex or condomless receptive anal intercourse with last partner and TFV-DP levels over time (P > .40, data not shown).
Three participants acquired an HIV infection during study follow-up: 1 each at 32, 36, and 48 weeks for an annualized HIV incidence of 6.4 (95% CI, 1.3-18.7) infections per 100 person-years. Tenofovir diphosphate levels for seroconverters are shown in Figure 3 and are all consistent with taking fewer than a mean of 2 doses per week at the likely time of HIV acquisition. No genotypic mutations conferring resistance to tenofovir or emtricitabine were detected by consensus sequencing at the time of diagnosis.
Compared with participants with protective levels of TFV-DP, those without protective levels were more likely to endorse the statement “I worry others will see me taking pills and think I am HIV-positive” (baseline, 4 participants [22.2%]; week 48, 5 participants [29.4%]; P = .03). The most commonly reported reasons for missing doses of the study medication were being away from home (n = 105, 32%), being too busy (n = 91, 28%), forgetting (n = 85, 26%), and changes in routine (n = 61, 18%). Participants could contribute more than once to the reporting of each reason. The acceptability of the pill size and pill taste decreased from 12 weeks to 48 weeks (“Liked a lot” range, 6 [10.2%] to 3 [7.1%]; P = .06; and “Liked a lot” range, 3 [5.0%] to 1 [2.4%]; P = .002; respectively), coincident with declines in biomarkers of adherence.
To our knowledge, ATN 113 is the first study on the safety and implementation of PrEP among adolescent MSM. This study demonstrates that adolescents who are at risk for HIV and therefore likely to benefit from PrEP can be enrolled in a biomedical HIV prevention clinical trial. A major challenge of this study was to ensure safe and unfettered access for at-risk minors to provide consent for their own participation in a clinical trial and to contribute crucial data for licensure.18,19
Acceptability ratings of PrEP, the overall study, and the study components were high. Preexposure prophylaxis was well tolerated by participants with no documented discontinuations because of adverse effects and no confirmed abnormal laboratory results. Peak bone mass, which is a potent predictor of fractures in later life19 is typically not achieved until late adolescence or early adulthood,20 so we expected to see overall increases in BMD among young men aged 15 to 17 years. On the other hand, the slight but statistically significant decline in total body BMD z score suggests that growth may have been less than would be predicted among this age group. The apparent lack of a strong association of change in BMD with magnitude of TFV exposure (week 48 dried blood spot TFV-DP levels) differs from results seen among adult MSM who use PrEP.21 However, we would caution that the relatively small sample size, coupled with the competing forces of bone growth and TDF-associated bone loss, make it difficult to draw conclusions about the effects of TDF on bone density levels in this age group. Further study, including follow-up measurements of changes in BMD after discontinuation of PrEP, is warranted to fully assess the potential risks and benefits of using TDF/FTC PrEP in this vulnerable population.
The incidence of STIs decreased among participants, but the HIV incidence rate was high compared with other open-label clinical trials in the United States4,6 and almost twice the rate found in the companion ATN 110 study that enrolled MSM who were aged 18 to 22 years.22 Those who had seroconversion had very low levels of drugs detected, if any, at the time of seroconversion. These results continue to strengthen and support the conclusion of the data that PrEP works when taken according to the prescribed dose.
Challenges with adherence to medication are commonplace among adolescents, regardless of whether it is adherence to a treatment or prevention regimen. Nonadherence among youth is often a reflection of both the biological and behavioral transitions that occur during this developmental time, including increased autonomy from parents/caregivers, increased importance of peers and corresponding vulnerability to peer influence and stigma, and an undeveloped cognitive capacity for organization and planning. Furthermore, low perceived HIV risk has been associated with low adherence in prevention clinical trials.23 Thus, it is not surprising that a proportion of adolescents in this study were unable to adhere with enough frequency to confer high levels of HIV protection. However, most participants were able to take at least 2 doses per week as estimated by TFV-DP levels, indicating that they were attempting to adhere to the regimen, albeit with less frequency than prescribed. Of critical importance will be the development and testing of long-acting PrEP agents for HIV prevention among adolescents that would likely reduce (although not eliminate) the adherence issues that are associated with daily pills.
A noticeable trend in the adherence data from this study, also seen in ATN 110, is the striking drop in TFV-DP levels once participants began the quarterly visit schedule. We have suggested that an augmented visit schedule, or at least the option of additional visits, might be most appropriate for youth.22 Indeed, this approach would be consistent with the US contraceptive practice recommendations, which already recognize that adolescents are a special population who might benefit from more frequent follow-up than adults.24 Additional developmentally appropriate methods of sustaining PrEP engagement and adherence include more frequent interactions via mobile technology for medication reminders or supportive check-ins, adherence support through clubs or groups, peer buddies, and other youth-focused methods of service delivery.25
In addition to addressing the individual-level barriers to adherence, more work is needed to address community-level barriers, such as the stigma and homophobia associated with PrEP. A Kaiser Foundation survey found that 84% of youth aged 15 to 24 years reported recognizing stigma around HIV in the United States26 and other studies have found that black MSM were more likely than other MSM to report experiencing PrEP-related stigma,27 as well as sexuality-related stigma.28 Anticipatory stigma from sexual partners has also been reported as a barrier to PrEP use.29 These multifaceted experiences with stigma ultimately limit access to PrEP for those who may benefit from it the most.
To our knowledge, ATN 113 is the first adolescent-specific PrEP clinical trial to be completed, but it will certainly not be the last, and there is much work to do. We need to better understand the barriers to adherence and develop more effective ways to enhance adherence for youth who are clinically prescribed PrEP. More research is needed to explore PrEP knowledge, the accuracy of risk perception, stigmas, and access problems among adolescents, as well as clinician competence.
For youth who are vulnerable to HIV infection, biomedical tools need to be leveraged and integrated with behavioral interventions. While it may be challenging to enroll youth into biomedical clinical trials, if youth are not enrolled then they cannot benefit from the regulatory approval of these life-saving tools. Conversely, if they are simply used off-label without the support of contextual and biomedical data from such trials, then the safest and most appropriate manner in which to use these tools in youth will remain unclear and barriers to access could become insurmountable.
This study has several limitations to be considered when interpreting the results. The small sample size of the study, along with lack of participation from some ATN sites, may limit the generalizability of the findings as representative of adolescent MSM in other geographic areas or sociodemographic categories. In addition, while rectal swabs and urine were collected for STI testing in this study, we did not conduct pharyngeal testing and samples were only routinely collected at baseline, 24 weeks, and 48 weeks. This sampling strategy may ultimately have underestimated the rates of STIs among this sample. Finally, the time and resources that were needed to conduct this study were substantial and may limit the ability to replicate these findings in future clinical trials.
The high incidence rates of HIV and STIs among YMSM, along with the lack of any significant safety signals from this study, strongly support the need for an adolescent PrEP indication for TDF/FTC. The waning adherence, especially with quarterly visits, demonstrates that more time, attention, and resources may need to be allocated to adolescents who are seeking prevention services. Developmentally appropriate visit schedules within adolescent-friendly service facilities will be important additions to PrEP implementation programs.
Corresponding Author: Sybil G. Hosek, PhD, Stroger Hospital of Cook County, 1900 W Polk St, Ste #854, Chicago, IL 60612 (firstname.lastname@example.org).
Accepted for Publication: May 17, 2017.
Published Online: September 5, 2017. doi:10.1001/jamapediatrics.2017.2007
Author Contributions: Dr Hosek had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.
Concept and design: Hosek, Landovitz, Kapogiannis, Siberry, Rudy, Rutledge, Liu, Mulligan, Zimet, Lally, Brothers, Rooney, Wilson.
Acquisition, analysis, or interpretation of data: Hosek, Landovitz, Kapogiannis, Siberry, Rudy, Rutledge, Liu, Harris, Zimet, Mayer, Anderson, Kiser, Brothers, Bojan, Rooney, Wilson.
Drafting of the manuscript: Hosek, Landovitz, Rudy, Rutledge, Mulligan, Wilson.
Critical revision of the manuscript for important intellectual content: Landovitz, Kapogiannis, Siberry, Rutledge, Liu, Harris, Mulligan, Zimet, Mayer, Anderson, Kiser, Lally, Brothers, Bojan, Rooney, Wilson.
Statistical analysis: Rutledge, Harris.
Obtained funding: Hosek, Lally, Wilson.
Administrative, technical, or material support: Hosek, Landovitz, Kapogiannis, Liu, Mulligan, Zimet, Anderson, Brothers, Bojan, Rooney, Wilson.
Supervision: Hosek, Landovitz, Kapogiannis, Rudy, Liu, Mulligan, Anderson, Lally, Brothers.
Other–PK analysis and interpretation: Kiser.
Conflict of Interest Disclosures: Dr Mayer receives grant support from Gilead Sciences and ViiV. Dr Anderson receives donated study drugs and contract work fees from Gilead. No other disclosures are reported.
Funding/Support: This study was supported by grants U01 HD 040533 and U01 HD 040474 (National Insitute of Child Health and Human Development medical officer, Dr Kapogiannis) the Adolescent Medicine Trials Network for HIV/AIDS Interventions from the National Institutes of Health through the National Institute of Child Health and Human Development and received research support from the National Institutes on Drug Abuse and Mental Health. Study drugs were donated by Gilead Sciences along with funding for a portion of the dried blood spot testing and overall study costs. Logistical support was provided by the Adolescent Medicine Trials Network for HIV/AIDS Interventions Coordinating Center (Principal Invesitgator, Dr Wilson) at The University of Alabama at Birmingham. Network operations and data management support was provided by the Adolescent Medicine Trials Network for HIV/AIDS Interventions Data and Operations Center at Westat.
Role of the Funder/Sponsor: The funding organizations had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.
Additional Contributions: We thank the principal investigators from the National Institutes on Drug Abuse (Katherine Davenny, MPH, and Shoshana Kahana, PhD), the National Institutes on Mental Health (Pim Brouwers, PhD, and Susannah Allison, PhD), the University of Alabama at Birmingham (Cynthia Partlow, MEd), and the Adolescent Medicine Trials Network for HIV/AIDS Interventions Data and Operations Center at Westat (Jim Korelitz, PhD, and Barbara Driver, RN, MS). We also thank the investigators and staff members at the following sites that participated in this study: Children’s Hospital of Los Angeles (Marvin Belzer, MD, and Diane Tucker, RN), Children’ s Hospital of Philadelphia (Steven D. Douglas, MD, Mary Tanney, MD, and Adrienne DiBenedetto, BSN), John H. Stroger Jr. Hospital of Cook County and the Ruth M. Rothstein CORE Center (Jaime Martinez, MD, Kelly Bojan, DNP, Rachel Jackson, MSN), Tulane University Health Sciences Center (Sue E. Abdalian, MD, Leslie Kozina, RN, Alyne Baker, RN), The Fenway Institute–Boston (Kenneth H. Mayer, MD, George, and Julian Dormitzer, BSN), and University of Colorado Denver (Craig McFarland, MD, Daniel Reirden, MD, and Amy E. Hahn, MD). Drug concentrations were assayed at the Colorado Antiviral Pharmacology Laboratory (Lane Bushman, Jia-Hua Zheng, PhD, L. Anthony Guida, Becky Kerr, BS, Brandon Klein). The investigators are grateful to the members of the local youth community advisory boards for their insight and counsel and are particularly indebted to the young men who participated in this study for their willingness to share their lives and their time with us.
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