Combination antiretroviral therapy (ART) regimens for HIV-1-infected patients are now more effective, safe and convenient. However, treatment adherence, emergence of resistant virus with virologic failure, and tolerability remain important challenges . Convenient once-daily, single-tablet regimens (STR) can facilitate treatment adherence and improve treatment effectiveness [2,3].
Since its initial approval in 2006, substantial clinical trial data and clinical experience with darunavir have accumulated, demonstrating the potent and durable virologic response, high genetic barrier to resistance, and favorable safety profile in ART-naive, HIV-1-infected patients [4,5]. A substantial proportion of newly diagnosed patients in the United States and Europe are treated with a boosted protease inhibitor [6,7], and darunavir is the recommended protease inhibitor in treatment guidelines [8–10]. United States guidelines recommend two nucleoside or nucleotide analogue reverse transcriptase inhibitors (NRTIs) combined with an integrase strand transfer inhibitor (INSTI), or in certain clinical situations boosted darunavir 800 mg once daily or a nonnucleoside reverse transcriptase inhibitor (NNRTI) [8,9]. Boosted darunavir is recommended for patients with uncertain adherence, those who require a regimen with a high-resistance barrier, or those patients without available resistance results . European guidelines recommend two NRTIs combined with either an INSTI, boosted darunavir or an NNRTI for all ART-naive patients , with both darunavir and atazanavir as recommended protease inhibitors in the BHIVA guidelines .
Phase-3 studies have established the noninferior antiviral efficacy and improved renal and bone safety of ART regimens containing tenofovir alafenamide (TAF), a newer tenofovir prodrug, vs. tenofovir disoproxil fumarate (TDF), combined with different third agents [12,13], making TAF an optimal backbone component.
Darunavir/cobicistat/emtricitabine/tenofovir alafenamide (D/C/F/TAF) 800/150/200/10 mg is the first and only once-daily protease inhibitor-containing STR in development, combining the antiviral efficacy, and resistance barrier of darunavir with the safety of TAF. D/C/F/TAF was approved for use in Europe in September 2017, and is investigational and currently undergoing regulatory review in the United States. D/C/F/TAF is being evaluated in two international, randomized, phase-3 studies: AMBER (NCT02431247) in ART-naive, HIV-1-infected adults, and EMERALD (NCT02269917) in treatment-experienced adults with virologically suppressed HIV infection . We present the 48-week primary analysis of AMBER, which evaluated D/C/F/TAF vs. darunavir/cobicistat in combination with emtricitabine/TDF (F/TDF).
AMBER (TMC114FD2HTX3001; ClinicalTrials.gov NCT02431247; EudraCT 2015–000754–38) is a phase-3, randomized, active-controlled, double-blind, noninferiority study being conducted at 121 sites across 10 countries in North America (USA, Canada) and Europe (Belgium, France, Germany, Italy, Poland, Russia, Spain, UK). The trial included a ∼30-day screening period (up to ≤6 weeks) and a 48-week treatment period. In addition, all patients continue to receive D/C/F/TAF in an open-label, single-arm treatment phase up to week 96, and then in a roll-over extension phase.
Participants were randomized (1 : 1) using a computer-generated interactive web-response system to receive D/C/F/TAF 800/150/200/10 mg (q.d.) daily or darunavir/cobicistat 800/150 mg fixed-dose combination (FDC) co-administered with F/TDF 200/300 mg FDC daily (control). Participants received placebo tablets matching the alternative treatment – three tablets in total – and were instructed to take all study drugs and matching placebo tablets with food at approximately the same time each morning. Randomization was stratified by screening viral load (≤ or >100 000 copies/ml) and CD4+ cell count (< or ≥200 cells/μl).
The trial was conducted in accordance with the principles of Good Clinical Practice and Declaration of Helsinki. The protocol and amendments were reviewed and approved by an institutional review board or independent ethics committee. All study participants provided written informed consent.
Eligible patients were treatment-naive, HIV-1-infected adults (≥18 years) with a screening plasma viral load at least 1000 copies/ml, CD4+ cell count greater than 50 cells/μl, genotypic sensitivity to darunavir, emtricitabine, and tenofovir (GenoSure MG HIV-1 protease/reverse transcriptase genotype assay; Monogram Biosciences, South San Francisco, California, USA), and an estimated glomerular filtration rate based on serum creatinine (eGFRcr) at least 70 ml/min (Cockcroft–Gault formula) . Main exclusion criteria included diagnosis of a new AIDS-defining condition within 30 days prior to screening, hepatitis B or C coinfection, clinically significant disease (e.g. malignancy, severe infections), and pregnancy or breastfeeding in women. Medications or herbal supplements known or suspected to have drug interactions with the investigational medications were disallowed.
Main study assessments and outcomes
Study visits were at baseline, weeks 2, 4, 8, and 12, and then every 12 weeks until week 96. Adverse events were graded according to the Division of AIDS grading table  and coded using the Medical Dictionary for Regulatory Activities (version 19.1). At each visit, urine and blood samples were collected for plasma viral load (COBAS AmpliPrep/COBAS TaqMan HIV-1 Test, V2.0; Roche Diagnostics, Basel, Switzerland) and CD4+ cell count determinations, biochemistry, hematology, urinalysis and urine chemistry, serum cystatin C for calculating eGFRcyst [Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) formula] , and serum creatinine for calculating eGFRcr (Cockcroft–Gault formula and CKD-EPI formula) [15,17]. Treatment adherence was monitored at each visit (except week 2) by drug accountability (pill count and patient log booklet). The renal proteinuria biomarkers, urinary retinol-binding protein (RBP), and beta-2-microglobulin were measured at baseline, weeks 2, 4, 12, 24, and 48 in the fasted state. Fasted metabolic profile assessments (total, high-density lipoprotein [HDL]-cholesterol and low-density lipoprotein [LDL]-cholesterol, triglycerides) were performed at baseline, weeks 24 and 48. Pharmacokinetic sampling was performed at weeks 2, 4, 8, 12, 24, 36, 48, and study endpoint.
Protocol-defined virologic failure (PDVF) was defined as virologic nonresponse (viral load <1 log10 reduction from baseline and ≥50 copies/ml at week 8, confirmed at next visit) or virologic rebound (confirmed viral load ≥50 copies/ml after confirmed, consecutive viral load <50 copies/ml or confirmed viral load >1 log10 increase from the nadir) and/or viremia at the final time point (viral load ≥400 copies/ml at study endpoint or study discontinuation after week 8). Post screening resistance testing (PhenoSense GT) was performed on samples from patients with PDVF and viral load greater or equal to 400 copies/ml at time of failure (preferably confirmed, or otherwise unconfirmed) or at later time points.
The primary objective was the noninferiority evaluation of D/C/F/TAF vs. darunavir/cobicistat co-administered with F/TDF in the proportion of patients with viral load less than 50 copies/ml (response rate) by the Food and Drug Administration (FDA)-snapshot analysis at week 48.
Secondary outcomes included proportion of patients with viral load <20 and <200 copies/ml (FDA-snapshot analysis) and viral load<50 copies/ml (time-to-loss-of-virologic-response algorithm) at week 48; changes from baseline in log10 viral load and CD4+ cell count; antiretroviral resistance development in PDVFs; safety and tolerability through 48 weeks; changes from baseline at week 48 in serum creatinine, eGFRcr, eGFRcyst, and ratios of total urine protein, urine albumin, urine RBP, and beta-2-microglobulin to creatinine (UPCR, UACR, RPB:Cr, and B2M:Cr, respectively).
Bone investigation substudy
The bone investigation substudy was performed at selected study sites in consenting participants from both randomization groups. Endpoints at weeks 24 and 48 were percentage changes from baseline in spine, hip, and femoral neck bone mineral density (BMD; measured by dual-energy X-ray absorptiometry scans); changes in associated T score (normal BMD defined as a T score ≥−1; osteopenia as a T score from ≥−2.5 to <−1; and osteoporosis as a T score <−2.5); and changes in bone biomarkers, alkaline phosphatase (ALP), procollagen type N-terminal propeptide (P1NP), C-type collagen sequence (CTX), parathyroid hormone (PTH), and 25-hydroxy vitamin (25[OH]D), measured in the fasted state.
The week-48 primary analysis was performed on the intent-to-treat population (constituting all patients who were randomized and received at least one dose of study drug). A per-protocol analysis was also performed, excluding patients with major protocol violations or other predefined criteria that potentially affected efficacy. Data analysis was performed using SAS software (SAS Institute, Inc, Cary, North Carolina, USA) version 9.2.
Assuming a response rate of 80% at week 48 (FDA-snapshot analysis) for both treatment groups, 335 patients needed to be enrolled in each group to establish noninferiority of D/C/F/TAF to control, with a noninferiority margin of 10% at 90% power and a one-sided significance level of 2.5%. For the bone investigation substudy, at least 85 patients per treatment group were required to detect an absolute difference between groups in BMD of at least 2% with 90% power, assuming a 4% inter-subject variability and a one-sided significance level of 2.5%.
Noninferiority of D/C/F/TAF to control would be demonstrated if the lower limit of the two-sided 95% confidence interval (CI) of the stratum-adjusted (viral load ≤100 000 or >100 000 copies/ml and CD4+ cell count <200 or ≥200 cells/μl) Mantel–Haenszel difference between treatment groups (D/C/F/TAF minus control) in the week-48 response rate was greater than −10%. Superiority would be established if the lower limit of the 95% CI was greater than 0.
The difference between groups in least square mean (LSM) change from baseline at week 48 in CD4+ cell count and associated 95% CIs were constructed using analysis of covariance (ANCOVA), including CD4+ cell count at baseline as a continuous covariate. In patients who discontinued, CD4+ cell count values after discontinuation were imputed with the baseline value (noncompleter = failure). For other missing values, the last observation was carried forward.
Baseline and postbaseline HIV-1 genotypes were analyzed for protease resistance-associated mutations (RAMs) [including International Antiviral Society (IAS)–USA primary PI RAMs] and reverse transcriptase RAMs (including IAS-USA NRTI RAMs and IAS–USA NNRTI RAMs), as well as specific RAMs to the study drugs . Antiretroviral sensitivity, based on the genotype/phenotype report, was also assessed.
Within-treatment comparisons of mean changes from baseline in renal and bone biomarkers, and fasting lipids were performed using the Wilcoxon signed-rank test. Between-treatment comparisons were assessed using the Wilcoxon rank-sum test. Between-treatment differences in change from baseline in serum creatinine, eGFR, and BMD were tested using ANCOVA, including treatment as a factor and corresponding baseline values as covariates.
Patient disposition and baseline characteristics
The study began on 6 July 2015, and the cut-off date for the week-48 primary analysis was 13 March 2017. Of 866 screened patients, 725 were randomized and included in the intent-to-treat population (Fig. 1); 362 received D/C/F/TAF and 363 received darunavir/cobicistat with F/TDF.
Through 48 weeks, 93.6% (339/362) of patients in the D/C/F/TAF group and 92.3% (335/363) in the control group completed therapy (Fig. 1). The most common reasons for discontinuing the study, as reported by the investigators, were adverse events, withdrawn consent, and loss to follow-up.
Baseline characteristics were balanced between the two groups (Table 1). Median age was 34 years, 88% were men, 83% were white, and 18% had viral load at least 100 000 copies/ml. Median baseline CD4+ cell count was 453 cells/μl.
As depicted by the protocol, at screening, all enrolled participants demonstrated genotypic sensitivity to darunavir, emtricitabine, and tenofovir based on the genotype report. Few had viruses with at least one darunavir RAMs (1%) or primary PI RAMs (2%) (Table 1). No RAMs related to emtricitabine or TDF/TAF were detected. NNRTI and NRTI RAMs were detected in 16 and 5% of patients, respectively (Table 1).
In the primary analysis of virologic response at week 48 (FDA-snapshot analysis), noninferiority of D/C/F/TAF [91.4% (331/362)] vs. control [88.4% (321/363)] was demonstrated (difference 2.7%; 95% CI −1.6 to 7.1; P < 0.0001; Fig. 2a and Supplemental Table S1, http://links.lww.com/QAD/B260). A low proportion of participants in the D/C/F/TAF group [4.4% (16/362)] and control group [3.3% (12/363)] had a viral load greater or equal to 50 copies/ml at week 48 (FDA-snapshot analysis).
Results from the per-protocol analysis confirmed noninferiority of D/C/F/TAF [94% (327/348)] to control [92.2% (317/344)] (difference 1.5%; 95% CI −2.3 to 5.2; P < 0.0001), as did other sensitivity analyses (Supplementary Table 2, http://links.lww.com/QAD/B260). Week-48 response rates (FDA-snapshot analysis) were consistent across a range of patient subgroups (Fig. 2b).
A similar proportion of patients in each group also achieved a viral load <200 or <20 copies/ml (FDA-snapshot analysis) at week 48 (Supplementary Table 2, http://links.lww.com/QAD/B260). LSM increases (P < 0.0001) from baseline in CD4+ cell count (noncompleter = failure) at week 48 were 190.5 cells/μl for D/C/F/TAF vs. 172.0 cells/μl for control (P = 0.213 between groups; Supplementary Table 2, http://links.lww.com/QAD/B260).
Through week 48, eight (D/C/F/TAF) and six (control) participants had PDVF, with paired screening and postbaseline on-treatment genotypes available for seven vs. two patients, respectively. No darunavir, primary protease inhibitor, or TDF/TAF RAMs emerged in any patient. An M184V/I mutation associated with phenotypic resistance to emtricitabine and lamivudine was identified in one patient receiving D/C/F/TAF. This patient harbored a K103N mutation at screening, indicating transmitted NNRTI (efavirenz and nevirapine) resistance. Although the patient appeared to have good adherence (≥95% based on pill count), darunavir plasma concentrations were low [32–192 ng/ml, except at week 4 (1440 ng/ml)], indicating nonadherence that resulted in the patient being discontinued from the study after week 48. All other participants had virus that remained susceptible to all drugs in the treatment regimens.
Through week 48, 88.3% (264/299) vs. 88.3% (271/307) of patients in the D/C/F/TAF and control groups, respectively, were at least 95% adherent as measured by pill count (all patients took three tablets daily based on the study design).
Safety profiles were similar between groups (Table 2). Most adverse events regardless of causality were grade 1 or 2. The most common (≥5% in either group) study drug-related adverse events through week 48 were diarrhea, rash, and nausea (Table 2). All episodes of study drug-related diarrhea were mild or moderate (grade 1 or 2) and mostly transient in duration. Only one patient in each group (0.3%) discontinued the study because of diarrhea. There were no nervous system study drug-related adverse events greater than 5% nor discontinuations in either group.
Renal adverse events regardless of causality occurred in 2% (7/362) of D/C/F/TAF vs. 6% (21/363) of control patients. No renal adverse events were suggestive of treatment-emergent proximal renal tubulopathy and no renal adverse events led to discontinuation.
Grades 3 and 4 adverse events regardless of causality, serious adverse events, and adverse event-related discontinuations were rare (Table 2). The only grade 4 adverse event reported for at least two patients was suicide attempt, reported in two (0.6%) patients in the control group. There were no deaths during the treatment phase in either group (Table 2). However, one patient in the control group died following grade 4 sepsis in the follow-up phase (11 days after last study drug intake), which was not considered related to study drug (Fig. 1). Incidences and types of laboratory abnormalities were similar in both treatment groups, being mostly grade 1 or 2.
Median changes from baseline at week 48 for fasting lipid parameters were higher for D/C/F/TAF than control (Table 2 and Supplementary Figure 1, http://links.lww.com/QAD/B260). Changes in HDL-cholesterol favored D/C/F/TAF and remaining lipid increases favored control, with a small, statistically significant difference in the change from baseline in total cholesterol/HDL-cholesterol ratio between groups. Six (1.7%) vs. two (0.6%) patients, respectively, initiated a lipid-lowering drug during the treatment period (P = 0.1770 between groups).
Serum creatinine increased from baseline to week 48 in the D/C/F/TAF group (4.8 μmol/l), consistent with cobicistat inhibition of creatinine tubular secretion , but less so than in the control group (8.2 μmol/l; P < 0.0001, ANCOVA D/C/F/TAF vs. control). Consequently, the mean decrease in eGFRcr (CKD-EPI formula) at week 48 was less for D/C/F/TAF than control (−5.9 vs. −9.3 ml/min per 1.73 m2, respectively; P < 0.0001, ANCOVA; Fig. 3a), although mean eGFRcr was within normal limits. However, mean eGFRcyst (CKD-EPI formula) actually increased at week 48, and the increase was greater for D/C/F/TAF than control (5.3 vs. 2.9 ml/min per 1.73 m2, respectively; P = 0.001, ANCOVA) (Fig. 3b).
At week 48, all quantitative measures demonstrated less proteinuria for D/C/F/TAF vs. control, as determined by mean changes from baseline in UPCR [−22.42 mg/g (SD 71.98) vs. −10.34 mg/g (118.18), respectively; P = 0.033], UACR [−2.45 mg/g (23.81) vs. −0.58 mg/g (68.93); P
= 0.003], RBP:Cr [16.84 μg/g (317.31) vs. 401.12 μg/g (2688.91); P < 0.0001], and B2M:Cr [−100.58 μg/g (788.60) vs. 837.63 μg/g (6122.87); P < 0.0001].
Baseline characteristics in the bone investigation substudy were well balanced between the D/C/F/TAF (N = 113) and control (N = 99) groups (Supplementary Table 3, http://links.lww.com/QAD/B260). Hip, lumbar spine, and femoral neck BMD from baseline to week 48 were stable with D/C/F/TAF (mean percentage change 0.21, −0.68, and −0.26% at each site, respectively; Fig. 3), whereas they decreased significantly at week 48 in the control group [−2.73, −2.38, and −2.97%, respectively; P < 0.0001 (hip and femoral neck) and P = 0.004 (spine) for between-treatment comparisons]. Fewer patients receiving D/C/F/TAF had at least 3% decreases from baseline in BMD at each site than in the control group. More patients had at least 3% increases in the D/C/F/TAF group (Supplementary Table 4, http://links.lww.com/QAD/B260). A similar trend was seen for at least 5 and at least 7% increases or decreases in BMD (Supplementary Table 4, http://links.lww.com/QAD/B260). At week 48, a greater proportion of participants receiving D/C/F/TAF had improvements in T score at each site than in the control group, and a smaller proportion of participants receiving D/C/F/TAF had worsening BMD status (Supplementary Table 4, http://links.lww.com/QAD/B260). Fractures occurred infrequently and were not different between groups [1.1% (4/362) D/C/F/TAF vs. 0.6% (2/363) control; P = 0.451]; all were traumatic and none were suspected to be osteoporotic. New antiosteoporotic treatment was started by 9/362 (2.5%) vs. 16/363 (4.4%) patients, respectively, during the treatment phase. Changes from baseline in bone biomarker levels (ALP, P1NP, CTX, and PTH) suggested less bone turnover for D/C/F/TAF than control (Supplementary Figure 2, http://links.lww.com/QAD/B260). 25[OH]D levels increased from baseline in both groups.
In this investigational phase-3, double-blinded, randomized, controlled trial, the D/C/F/TAF once-daily STR was virologically noninferior to darunavir/cobicistat co-administered with F/TDF in ART-naive patients. Response rates were similar across age, sex, race, and baseline HIV characteristics including CD4+ cell count less than 200 cells/μl and viral load greater than 100 000 copies/ml. Although INSTI-based regimens have rapidly moved up in global treatment guidelines [8–10], there are still many patients who might benefit from the established characteristics of the protease inhibitor darunavir, such as high genetic barrier to resistance, efficacy in the face of resistance and uncertain adherence, provider comfort, and experience. Well powered, phase-3, double-blinded, randomized studies provide the most rigorous evidence to drive treatment guidelines. The week-48 virologic response rate (FDA-snapshot analysis) of 91.4% for D/C/F/TAF was among the highest achieved by a STR in phase-3 trials (range 80–93%) of ART-naive patients [12,20–26], and higher than in prior phase-3 trials with darunavir [4,23,27,28].
No treatment-emergent mutations associated with darunavir or tenofovir resistance were observed. Only one patient (D/C/F/TAF) was found to have M184I/V, conferring resistance to emtricitabine; this patient also had a transmitted K103N mutation at screening. M184V was detected pretreatment by deep sequencing (Illumina MiSeq) as a minority variant (9.4%). In addition, for this patient, darunavir plasma concentrations were low and much lower than the steady-state predose concentration (∼692 ng/ml), indicating potential nonadherence, which in fact resulted in discontinuation from the study. The observation of no darunavir phenotypic resistance and the genotypic results are consistent with previous darunavir studies [4,5,27,29], confirming the high resistance barrier of darunavir-based initial ART with no emergence of DRV resistance. D/C/F/TAF is the only STR in development that combines the high barrier to resistance of darunavir with the F/TAF backbone. In this context, D/C/F/TAF may have an important role for treating patients with uncertain adherence or who plan to start treatment prior to the availability of resistance-testing results . Patients with transmitted NNRTI and NRTI resistance were included in the study. As D/C/F/TAF does not require HLA B*5701 screening or hepatitis or resistance testing before treatment initiation, it is currently being evaluated in a rapid initiation protocol (NCT03227861). These characteristics suggest D/C/F/TAF is a highly feasible option in a test and treat setting or for very early treatment-naive patients where rapid combination ART initiation could be warranted.
Safety profiles were similar between the two treatment groups. However, adverse event-related discontinuations were lower for D/C/F/TAF (2%) than control (4%), and similar to those reported in phase-3 studies of other recently approved STRs [12,20–26]. The low incidences and similar types of adverse events, grade 3 or 4 adverse events, and serious adverse events between groups reflects the well characterized safety profiles for darunavir and cobicistat reported previously [4,27,29]. Given the low incidence of nervous system adverse events, D/C/F/TAF may be an important treatment option for ART-naive patients at risk of nervous system adverse events, such as insomnia and depression.
Less renal tubular proteinuria, and more favorable hip and spine BMD for D/C/F/TAF compared with control are consistent with TAF vs. TDF effects [12,13,29–31]. The improvement in eGFRcyst could reflect ART-related improvement in HIV-associated renal impairment, as was seen in the START study . The favorable renal tubular and BMD outcomes at the 48-week time point are reassuring, given the fact that the cumulative adverse effects of TDF on renal and bone outcomes have been greater whenever TDF was combined with boosted protease inhibitors . Median increases from baseline in fasting lipids were higher for D/C/F/TAF vs. control, with the increase in HDL-cholesterol favoring D/C/F/TAF and remaining lipid increases favoring control. There was a small, statistically significant difference in the total cholesterol/HDL-cholesterol ratio between groups. Differences in lipid profiles were likely because of the loss of the lipid-lowering effect of TDF rather than an adverse effect of TAF or any other of the components on lipids [12,13].
As in other recent phase-3 trials in ART-naive patients [20–26], study limitations were inclusion of more than 80% white patients and a comparatively small proportion of female or older (>50 years) participants or who had high viral loads. The latter most likely reflects earlier initiation of ART based on current guideline recommendations [8–11]. Phase-3 studies often lack power to detect rare clinical safety events; however, the large clinical safety database for darunavir and substantial clinical experience counterbalance this limitation. Renal and bone safety were assessed using surrogate markers rather than clinical events, and bone safety was assessed in a smaller number of patients.
In conclusion, D/C/F/TAF was noninferior to a regimen of darunavir/cobicistat co-administered with F/TDF at week 48, with a high virologic response (91.4%) in ART-naive, HIV-1-infected adults. D/C/F/TAF was associated with a better bone and renal safety profile than control, with few moderate, severe, or serious adverse events. Changes in HDL-cholesterol favored D/C/F/TAF and remaining lipid increases favored control. D/C/F/TAF is a novel STR that combines the known efficacy and high-genetic barrier to resistance of darunavir with the safety advantages of TAF to provide a new option for the treatment of ART-naive, HIV-1-infected patients.
This study was sponsored by Janssen.
We thank the patients and their families for their participation and support during the study, the central and local Janssen AMBER study teams, study center staff, and the principal investigators:
Belgium: S. De Wit, E. Florence, L. Vandekerckhove, B. Vandercam; Canada: J. Brunetta, M. Klein, D. Murphy, A. Rachlis, S. Walmsley; France: F. Ajana, L. Cotte, P.-M. Girard, C. Katlama, J.-M. Molina, I. Poizot-Martin, F. Raffi, D. Rey, J. Reynes, E. Teicher, Y. Yazdanpanah; Germany: K. Arastéh, M. Bickel, J. Bogner, S. Esser, G. Faetkenheuer, H. Jessen, W. Kern, J. Rockstroh, C. Spinner, H.-J. Stellbrink, A. Stoehr; Italy: A. Antinori, F. Castelli, A. Chirianni, A. De Luca, A. Di Biagio, M. Galli, A. Lazzarin, F. Maggiolo, R. Maserati, C. Mussini; Poland: A. Garlicki, J. Gasiorowski, W. Halota, A. Horban, M. Parczewski, A. Piekarska; Russia: E. Belonosova, O. Chernova, N. Dushkina, V. Kulagin, E. Ryamova, A. Shuldyakov, N. Sizova, O. Tsybakova, E. Voronin, A. Yakovlev; Spain: A. Antela, J.R. Arribas, J. Berenguer, J. Casado, V. Estrada, M.J. Galindo, M. Garcia Del Toro, J.M. Gatell, M. Gorgolas, F. Gutierrez, M.D.M. Gutierrez, E. Negredo, J.A. Pineda, D. Podzamczer, J. Portilla Sogorb, A. Rivero, R. Rubio, P. Viciana, I. De Los Santos; UK: A. Clarke, B.G. Gazzard, M.A. Johnson, C. Orkin, I. Reeves, L. Waters; United States: P. Benson, L. Bhatti, F. Bredeek, G. Crofoot, D. Cunningham, E. DeJesus, J. Eron, F. Felizarta, R. Franco, J. Gallant, D. Hagins, K. Henry, D. Jayaweera, C. Lucasti, C. Martorell, C. McDonald, J. McGowan, A. Mills, J. Morales-Ramirez, D. Prelutsky, M. Ramgopal, B. Rashbaum, P. Ruane, J. Slim, A. Wilkin, J. deVente.
We also thank other Janssen staff members for their input into this manuscript. We acknowledge Ian Woolveridge of Zoetic Science, an Ashfield company, Macclesfield, UK, for assistance in drafting the manuscript and coordinating and collating author contributions, which was funded by Janssen. Week-48 data were presented in part at the 16th European AIDS Conference, 25–27 October 2017, Milan, Italy.
Contributors: J.G., C.O., J.-M.M., E.N., A.A., A.M., J.E., and J.R. were investigators in the study and reported data for the patients. E.V.L., E.L., V.H., J.J., S.V., and M.O. were involved in the data analyses. All authors had full access to the data, were involved in the development of the primary manuscript and interpretation of data, have read and approved the final version, and have met the criteria for authorship as established by the ICMJE. The corresponding author had final responsibility to submit the manuscript for publication.
Conflicts of interest
Source of funding: This study was sponsored by Janssen. The funder was involved in the study design, study conduct, data collection, and data analysis.
J.E. has received research grants from Janssen, Gilead Sciences, and ViiV Healthcare, and has served as a consultant to Bristol Myers Squibb (BMS), Merck, Janssen, Gilead Sciences, and ViiV Healthcare. C.O. has received speaker honoraria or consulting fees for attending speakers’ bureaus or advisory boards and research grants from Janssen, Merck, ViiV Healthcare, and Gilead Sciences. J.G. has received consulting fees or advisory board honoraria from BMS, Gilead Sciences, Merck, ViiV Healthcare, and Theratechnolgies, and research grants from AbbVie, BMS, Gilead Sciences, Janssen Therapeutics, Merck, Sangamo Biosciences, and ViiV Healthcare/GlaxoSmithKline. He has since become a full-time employee of Gilead Sciences. J.-M.M. has participated in advisory boards for Merck, Gilead Sciences, Janssen, ViiV Healthcare, BMS, and Teva, and a speakers’ bureau for Gilead. He has received research grants from Merck and Gilead Sciences. E.N. has received speaker honoraria or consulting fees from ViiV Healthcare, Merck, Janssen Cilag, BMS, Gilead Sciences, and AbbVie. A.A. has served as a consultant to BMS, Gilead Sciences, Janssen Cilag, Merck, ViiV Healthcare, and AbbVie. He has received institutional research grants from BMS, Gilead Sciences, Janssen Cilag, and ViiV Healthcare. A.M. has received grants and personal fees from Gilead Sciences, ViiV Healthcare, Janssen and Merck, and grants from BMS and Sangamo. J.R. has received grants and personal fees from Janssen, Gilead Sciences, Merck, and ViiV Healthcare. E.V.L., E.L., V.H., J.J., S.V., and M.O. are all full-time employees of Janssen and potential stockholders of Johnson and Johnson.
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