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Verxve 144-Week Results: Nevirapine Extended Release (NVP XR) Qd Versus NVP Immediate Release (IR) Bid with FTC/TDF in Treatment-Naandiuml;ve HIV-1 Patients
ISSN 2155-6113
Journal of AIDS & Clinical Research

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Verxve 144-Week Results: Nevirapine Extended Release (NVP XR) Qd Versus NVP Immediate Release (IR) Bid with FTC/TDF in Treatment-Naïve HIV-1 Patients

Brinson C1*, Bogner JR2, Nelson M3, Podzamczer D4, Quinson AM5, Drulak M5, Andrade-Villanueva J6, Cahn P7, Santiago S8 and Gathe J9

1Central Texas Clinical Research, Austin, TX, USA

2University Hospital of Munich, Munich, Germany

3St Stephen’s AIDS Trust, London, UK

4Hospital Universitari de Bellvitge, Barcelona, Spain

5Boehringer Ingelheim Pharmaceuticals, Inc, Ridgefield, CT, USA

6Universidad de Guadalajara, Guadalajara, Mexico

7Fundación Huspéd, Buenos Aires, Argentina

8Care Resource, Miami, FL, USA

9Therapeutic Concepts, Houston, TX, USA

*Corresponding Author:
Cynthia Brinson
Central Texas Clinical Research
Austin, TX 78751
Tel: 512-480-9270
E-mail: [email protected]

Received Date: June 24, 2013; Accepted Date: August 20, 2013; Published Date: August 25, 2013

Citation: Brinson C, Bogner JR, Nelson M, Podzamczer D, Quinson AM, et al. (2013) Verxve 144-Week Results: Nevirapine Extended Release (NVP XR) Qd Versus NVP Immediate Release (IR) Bid with FTC/TDF in Treatment-Naïve HIV-1 Patients. J AIDS Clin Res 4:233. doi:10.4172/2155-6113.1000233

Copyright: © 2013 Brinson C, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Background: We report 96- and 144-week follow-up data from VERxVE, demonstrating that nevirapine (NVP) extended release (XR) 400 mg once daily was non-inferior to NVP immediate release (IR) 200 mg twice daily, each administered on a backbone of emtricitabine/tenofovir. Methods: VERxVE was a double-blind, double-dummy, non-inferiority study in adults with screening viral load (VL) >1000 copies/mL and CD4+ cell count <400 cells/mm3 (males) or <250 cells/mm3 (females). Randomisation was stratified by baseline VL (copies/mL) ≤ 100,000 or >100,000. The primary endpoint was confirmed virologic response (<50 copies/mL) at week 48. Cochran’s statistic incorporating baseline VL strata tested non-inferiority of XR efficacy versus IR. Secondary endpoints included 144-week sustained virologic response and safety. Results: In all, 1011 patients were randomised and treated with NVP: 736 (XR n=378; IR n= 358) completed 144 weeks. Virologic response was 63.6% for NVP XR and 58.5% for NVP IR (adjusted difference of 4.8% [95% confidence interval –1.1% to 10.8%] favouring NVP XR). No significant differences were seen in changes in CD4+ T-cell counts from baseline, virologic failures or total discontinuation rates between treatment arms, regardless of demographic or baseline characteristics. Conclusions: NVP XR demonstrated non-inferior virologic efficacy to NVP IR in treatment-naïve HIV-infected patients and was well tolerated out to week 144, with a safety profile similar to NVP IR.


HIV; Nevirapine; Clinical trial; Extended-release formulation; Once-daily dosing


Non-nucleoside reverses transcriptase inhibitor (NNRTI)-based antiretroviral (ARV) regimens are important options for the initial treatment of HIV-1 infection. Nevirapine (NVP; Viramune®, Boehringer Ingelheim Pharmaceuticals, Ridgefield, CT, USA) was the first NNRTI to be approved by the US Food and Drug Administration in 1996, and NVP-based ARV regimens have been widely used around the world. As a result, the safety and efficacy profiles of NVP are well understood and established in various patient populations.

One of the key benefits of NVP is the lack of untoward effects of this ARV on serum lipid profiles, which have been reported with other anti-HIV drugs. Elevation of serum lipid risk categories can be a significant concern for HIV-infected patients, who tend to have elevated cardiovascular risk profiles as a direct result of viral infection, which can be further aggravated by some ARVs, especially some HIV protease inhibitors.

The extended-release (XR) formulation of NVP 400 mg (NVP XR) was developed to allow once-daily (qd) dosing, since this regimen has been shown to increase patient compliance, regimen adherence and therapeutic benefit, especially in homeless or marginally housed populations [1-3].

VERxVE [4] was a double-blind, double-dummy, non-inferiority phase III clinical trial comparing efficacy and safety of the qd formulation of NVP XR 400 mg versus the immediate-release (IR) formulation of NVP (200 mg twice daily [bid]). A total of 1011 patients meeting the screening criteria of viral load (VL) >1000 copies/mL and CD4+ cell count <400 cells/mm3 (males) or <250 cells/mm3 (females) were randomised. Over 48 weeks (the primary endpoint in this study), the NVP XR formulation demonstrated non-inferior efficacy compared with NVP IR. In addition, both the XR and the IR formulations demonstrated equivalent adverse event (AE) and tolerability profiles at the 48-week time point.

Herein we report the efficacy and safety results of the 96- and 144- week follow-up of NVP XR versus NVP IR antiviral therapy (ART), each administered on a backbone of emtricitabine/tenofovir, in treatment-naïve HIV-1 patients.


The details of the methods used in the VERxVE study have been described in detail in the 48-week report (4), and are herein described briefly. VERxVE, a randomised, double-blind, double-dummy noninferiority (-10% margin), parallel-group, active-controlled trial in adult, ART-naïve, HIV-1 infected patients, compared the efficacy and safety of NVP XR (400 mg qd) with NVP IR (200 mg bid), both administered in combination with emtricitabine/tenofovir once-daily. Eligible patients were stratified by baseline HIV-1 viral load into two groups 1) low ≤ 100,000 copies/mL , and 2) high >100,000 copies/mL. Patients who successfully completed the 14-day lead-in period during which they received NVP IR (200 mg qd) were randomised to either NVP XR 400 mg qd or NVP IR 200 mg bid (Figure 1).


Figure 1: Study design of the VERxVE trial. bid, twice daily; FTC/TDF, emtricitabine/tenofovir; NVP, nevirapine; qd, once daily.

The treatment period was 48 weeks (primary endpoint), with a blinded extension to 144 weeks, which continued after each patient had completed the week 48 visit.

At the conclusion of the 144-week blinded treatment period, patients had the option to enter the open-label extension phase, where they received NVP XR and continued emtricitabine/tenofovir qd treatment (Figure 1). Open-label extension participants visited the clinic every 12 weeks until the last patient enrolled in the trial completed the 144-week blinded treatment phase. At that point, each patient was scheduled for an end-of-trial visit (within 30 days) to gather final long-term safety and efficacy data.

The primary endpoint for VERxVE was confirmed virologic response at week 48. The secondary endpoints included sustained virologic response (SVR), using lower limit of quantification [LLOQ] of 50 copies/mL, and safety outcomes at weeks 96 and 144. Virologic response was defined as two consecutive VL measurements <50 copies/ mL (at least 2 week apart). In order to be considered an SVR, there could be no viral rebound or change in ART through week 144.

The major criteria for patient inclusion were: (i) adult (≥ 18 years of age) HIV-1-infected patients with no prior ART; (ii) CD4+ counts >50 to <400 copies/mL in males or >50 to<250 copies/mL in females; (iii) baseline HIV-1 VL ≥ 1000 copies/mL; and (iv) Karnofsky score >70.

The Cochran’s statistic with variance correction was used to calculate the difference and 95% confidence interval (CI) between the two NVP formulations (XR vs. IR). The non-inferior efficacy of NVP XR versus NVP IR was determined by a lower limit of the CI greater than -10%. All of the safety parameters reported here are presented descriptively.



Baseline characteristics, including mean HIV VL, proportion of patients in each VL category and mean CD4+ T-cell count, were similar between the two treatment arms (Table 1) [4]. VERxVE study results at 48 weeks have been previously reported [4].

  n = 508 n = 505
Baseline HIV (log10 copies/mL), n    
Mean 4.7 4.7
SD 0.6 0.7
Median 4.7 4.7
Baseline HIV RNA (copies/mL), n (%)    
<1,000 2 (0.4) 3 (0.6)
1,000 to 10,000 82  (16.1) 77  (15.2)
>10,000 to 100,000 250  (49.2) 260  (51.5)
>100,000 to 1,000,000 167  (32.9) 155  (30.7)
>1,000,000 7  (1.4) 10  (2.0)
Baseline CD4+ T-cell count, cells/mm2    
n 507 503
Mean 227.7 229.6
SD 85.9 81.4
Median 224.5 227.5

Table 1: Patient demographics and baseline characteristics.

Patient disposition at 144 weeks

At 144 weeks, 70.8% (n=358/506) of patients originally on the IR formulation were still receiving NVP IR and 74.9% (n=378/505) who were originally receiving the XR formulation remained on the XR formulation. Medication discontinuation was similar in both groups, wherein 29.2% (n=148/506) of patients discontinued NVP IR and 25.1% (n=127/505) of patients discontinued NVP XR. Patients in the IR arm who completed the 144 weeks of treatment were given the option of switching to the extended-release formulation (NVP XR) and continuing in the open-label extension of the study. In all, 315 patients in the IR arm exercised this option (Figure 2).


Figure 2: Patient disposition through week 144 and beyond in the openlabel extension. NVP IR, nevirapine immediate release; NVP XR, nevirapine extended release; XR, extended release.


The SVR, based on an LLOQ of 50 copies/mL by time to loss of virologic response (TLOVR; full analysis set), was similar between the two arms at each time point of the study; however, both groups demonstrated declining SVR rates over the long-term follow-up, from week 48 to week 144 (Figure 3). At week 144, SVR was achieved in 63.56% (n=321/505) of patients receiving NVP XR qd formulation, compared with 58.5% (n=296/506) of patients receiving the NVP IR bid formulation.


Figure 3: Proportion of patients with sustained virologic response at weeks 48, 96 and 144, by TLOVR. NVP IR, nevirapine immediate release; NVP XR, nevirapine extended release; SVR, sustained virologic response; TLOVR, time to loss of virologic response.

At week 144, the adjusted difference in the proportion of SVR for the XR and IR treatment groups was 4.84% (95% CI -1.11% to 10.79%) favouring NVP XR. The lower bound of CI excluded the -10% non-inferiority margin (P < 0.0001 for the non-inferiority test). By SNAPSHOT analysis, the adjusted difference in SVR proportions between the XR and IR formulations was 4.08% (95% CI -1.75% to 9.91%), favouring NVP XR.

At week 144, no associations between patient demographics (age group, gender, race, ethnicity or region) or patient baseline characteristics (CD4+ count, HIV subtype and CDC class) were associated with SVR in either treatment group. Patients with lower VL (<100,000) at baseline generally achieved a higher rate of SVR versus patients with higher VL (>100,000) at baseline, for both NVP formulations.

By TLOVR analysis, no clinically important differences were noted in the change in VL from week 48 to week 144 results between the IR and XR NVP formulations, i.e. results achieved by week 48 were generally maintained to week 144.

Patients in both treatment arms showed improvement in their CD4+ T-cell counts over the course of the trial, and this positive trend continued through 144 weeks. As seen in Figure 4, progressive increases from baseline in CD4+ T-cell counts with IR versus XR treatment, respectively, were seen at weeks 48 (207 vs. 213), 96 (257 vs. 275) and 144 (286 vs. 317).


Figure 4: Changes in CD4+ T-cell counts from baseline at weeks 48, 96 and 144.

Safety and tolerability out to week 144

The overall safety and tolerability results in patients receiving both the XR and the IR formulations of NVP at week 144 were similar to results reported at weeks 48 and 96. It is important to note that the rate of AEs, drug-related AEs (investigator-defined), serious AEs and Division of Acquired Immunodeficiency Syndrome (DAIDS) grade 3 and grade 4 AEs were similar between the two treatment groups out to week 96 and week 144 (Table 2).

  Up to week 96 FAS Up to week 144 FAS IR patients in open-label extension (post- week 144)
  NVP  IR 200 mg bid N = 506 n (%) NVP XR 400 mg qd N = 505 n (%) NVP  IR 200 mg bid N = 506 n (%) NVP XR 400 mg qd N = 505 n (%) NVP XR 400 mg qd N = 315 n (%)
Any AE 470 (92.9) 459 (90.9) 472 (93.3) 471 (93.3) 141 (44.8)
Investigator-defined drug-related AE 134 (26.5) 109 (21.6) 135 (26.7) 118 (23.4) 5 (1.6)
AEs leading to discontinuation of trial drug 52 (10.3) 44 (8.7) 54 (10.7) 43 (8.5) 0 (0.0)
Serious AEs* 76 (15.0) 78 (15.4) 83 (16.4) 93 (18.4) 9 (2.9)
Fatal 5 (1.0) 3 (0.6) 7 (1.4) 3 (0.6) 0 (0.0)
Immediately life-threatening 3 (0.6) 3 (0.6) 5 (1.0) 5 (1.0) 0 (0.0)
Disability/incapacity 0 (0.0) 0 (0.0) 1 (0.2) 1 (0.2) 1 (0.3)
Required hospitalisation 65 (12.8) 68 (13.5) 71 (14.0) 81 (16.0) 8 (2.5)
Prolonged hospitalisation 4 (0.8) 3 (0.6) 4 (0.8) 4 (0.8) 0 (0.0)
Congenital anomaly 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0)
Other 9 (1.8) 10 (2.0) 11 (2.2) 12 (2.4) 1 (0.3)
DAIDS grade 3 or 4 AEs 112 (22.1) 94 (8.6) 124 (24.5) 111 (22.0) 8 (2.5)
DAIDS grade 4 AEs 26 (5.1) 21 (4.2) 28 (5.5) 25 (5.0) 3 (1.0)
Study drug–related DAIDS grade 3 or 4 AEs 38 (7.5) 28 (5.5) 39 (7.7) 29 (5.7) 0 (0.0)
Study drug–related DAIDS grade 4 AEs 11 (2.2) 7 (1.4) 11 (2.2) 7 (1.4) 0 (0.0)

Table 2: Summary of overall adverse events: up to week 96 and 144 FAS (randomized phase), and open-label extension (beyond week 144).

With regard to severity of AEs, the majority of patients in both treatment groups reported either mild or moderate events. The frequency of patients reporting liver abnormalities or rashes did not change in any clinically meaningful way at the week 48, 96 and 144 follow-up visits.

Up to week 96 there were a total of 4 (0.4%, N=1,011) of patients with Stevens-Johnson syndrome (investigator defined as drug related), all of which were in the nevirapine IR group. This represents an increase of one patient since the Week 48 assessment, where three cases were noted. No new cases of Stevens Johnson syndrome were reported after week 96.

There were a total of 16 deaths in the VERxVE trial; none were attributed to study medication. Ten deaths were reported in the first 48 weeks, four deaths were reported between 48 and 96 weeks and two additional deaths reported after 96 weeks.

It is important to note that no novel or additional safety findings were reported after the 48-week time point and up to weeks 96 and 144.

Safety and tolerability beyond week 144: the open-label extension

In the open-label extension phase of the trial, when patients who had been on the IR formulation of NVP for 144 weeks had the option of switching to the XR qd formulation, the rate of all reported AEs, including drug-related AEs (investigator defined), serious AEs and DAIDS grade 3 and grade 4, were all lower in patients in the open-label extension.


A particular strength of this trial was the double-blind, doubledummy design, which ensured complete blinding of patients to the investigators and sponsor staff prior to week 48. Patients and investigators continued to be blinded to treatment group assignments after week 48.

In all, 1011 patients in VERxVE successfully completed NVP lead-in dosing, and began the randomised treatment period. The demographic data and baseline characteristics were also well balanced between patients randomised into the treatment groups.

The non-inferior efficacy of the XR formulation of NVP for the treatment of HIV-1 infection in patients who began ART for the first time was established at the week 48 analysis of virologic response [4]. The results at this time point also indicated similar safety and tolerability between the two treatment arms, with similar rates of all reported AEs, including drug-related AEs (investigator-defined), serious AEs and DAIDS grade 3 and grade 4 AEs, between the two treatment arms [4].

The present report describes long-term follow-up data from these patients after 96 and 144 weeks of treatment. These data demonstrate that the XR formulation of NVP (400 mg qd) continued to demonstrate virologic non-inferiority compared with the IR formulation (200 mg bid) as measured by SVR (VL <50 copies/mL). The efficacy results presented here continue to demonstrate that NVP XR is non-inferior to NVP IR with regard to HIV-1 VL suppression at up to and beyond week 144 in ART-naïve HIV-1-positive patients.

In addition, at week 144, the XR qd formulation continued to be well tolerated, with a safety profile equivalent to that seen with the IR bid formulation over the same follow-up time course. No significant or meaningful differences were observed between the two treatment arms with regard to TLOVR, change from baseline in HIV-1 VL at week 144, change in CD4+ cell count from baseline at week 144 or time to emergence of new AIDS-defining events, AIDS-related progression of events or death.

With regard to the long-term safety, i.e. efficacy and tolerability of NVP-based regimens, patients in the open-label extension phase of the trial (who had already completed 144 weeks of NVP IR treatment and had the option of switching to the XR qd formulation), demonstrated that the rate of reported AEs, including drug-related AEs (investigator defined), serious AEs and DAIDS grade 3 and grade 4 AEs, were all lower in patients in the open-label extension.

Once-daily formulations of antiretroviral medications can be especially advantageous for the manegment of HIV-infected patients from disadvantaged populations, including homeless or marginally housed patients (5). In these populations, the convenience of oncedaily administration significantly enhance patient adherence to ARV regimens, which has been shown to reduce the incidence of virologic breakthrough, and the emergence of virologic resistance [5].

The 96 and 144 week data presented in this paper strongly suggest the long-term durability of NVP XR-based regimens for treatmentnaïve HIV-1 patients.


This work was supported by Boehringer Ingelheim Pharmaceuticals, Inc. (BIPI). Writing, editorial support and formatting assistance was provided by José L. Walewski, PhD, of Envision Scientific Solutions, which was contracted and compensated by BIPI for these services.


The authors meet criteria for authorship as recommended by the International Committee of Medical Journal Editors (ICMJE) and were fully responsible for all content and editorial decisions, and were involved at all stages of manuscript development. The authors received no compensation related to the development of the manuscript, but are consultants for Boehringer Ingelheim Pharmaceuticals Inc (BIPI) and received research grant support from BIPI for this study.

Dr Quinson and Dr Drulak are employees of BIPI.

Dr Brinson is a consultant with Gilead Sciences, Inc.

Dr Gathe is a consultant with Gilead Sciences Inc, GlaxoSmithKline Inc., Pfizer Inc, Bristol-Myers Squibb Company, Abbott Laboratories, Janssen Pharmaceuticals Inc., Roche, Merck and Co., Tibotec Therapeutics and ViiV Healthcare.

Dr Bogner discloses his role as a speaker for most all manufactures of anti-HIV compounds, and has participated in AD-Boards with Abbott Laboratories, Janssen Pharmaceuticals Inc. and BIPI.

Dr Andrade-Villanueva, Dr Cahn, Santiago, Dr Podzamczer and Dr Nelson do not have any relationships to disclose.


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