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Volumn 28, Issue 5, 2012, Pages 437-446

Long-term efficacy, safety, and tolerability of rilpivirine (RPV, TMC278) in HIV type 1-infected antiretroviral-naive patients: Week 192 results from a phase IIb randomized trial

Author keywords

[No Author keywords available]

Indexed keywords

CHOLESTEROL; EFAVIRENZ; HIGH DENSITY LIPOPROTEIN CHOLESTEROL; LOW DENSITY LIPOPROTEIN CHOLESTEROL; RILPIVIRINE; TRIACYLGLYCEROL;

EID: 84860455337     PISSN: 08892229     EISSN: 19318405     Source Type: Journal    
DOI: 10.1089/aid.2011.0050     Document Type: Article
Times cited : (49)

References (18)
  • 1
    • 34548303425 scopus 로고    scopus 로고
    • The first once-daily single-tablet regimen for the treatment of HIV-infected patients
    • DOI 10.1358/dot.2007.43.7.1086178
    • Killingley B and Pozniak A: The first once-daily single-tablet regimen for the treatment of HIV-infected patients. Drugs Today 2007;43:427-442. (Pubitemid 47344920)
    • (2007) Drugs of Today , vol.43 , Issue.7 , pp. 427-442
    • Killingley, B.1    Pozniak, A.2
  • 2
    • 84916226318 scopus 로고    scopus 로고
    • Bristol-Myers Squibb Company. Available atAccessed February 3, 2011
    • FDA label for Sustiva (efavirenz) capsules and tablets. Bristol-Myers Squibb Company. 2010. Available at http:// packageinserts.bms.com/pi/pi-sustiva. pdf. Accessed February 3, 2011.
    • (2010) FDA Label for Sustiva (Efavirenz) Capsules and Tablets
  • 5
    • 75749118495 scopus 로고    scopus 로고
    • TMC278, a next-generation NNRTI, active against wild-type and NNRTI-resistant HIV-1
    • Azijn H, Tirry I, Vingerhoets J, et al.: TMC278, a next-generation NNRTI, active against wild-type and NNRTI-resistant HIV-1. Antimicrob Agents Chemother 2010;54:718-727.
    • (2010) Antimicrob Agents Chemother , vol.54 , pp. 718-727
    • Azijn, H.1    Tirry, I.2    Vingerhoets, J.3
  • 6
    • 70449368908 scopus 로고    scopus 로고
    • Efficacy and safety of etravirine in treatment-experienced, HIV-1 patients: Pooled 48 week analysis of two randomized, controlled trials
    • Katlama C, Haubrich R, Lalezari J, et al.: Efficacy and safety of etravirine in treatment-experienced, HIV-1 patients: Pooled 48 week analysis of two randomized, controlled trials. AIDS 2009;23:2289-2300.
    • (2009) AIDS , vol.23 , pp. 2289-2300
    • Katlama, C.1    Haubrich, R.2    Lalezari, J.3
  • 7
    • 79960343840 scopus 로고    scopus 로고
    • Accessed May 28, 2011
    • FDA label for EDURANTTM (rilpivirine) tablets. 2011. www .accessdata.fda.gov/drugsatfda-docs/label/2011/202022s000lbl .pdf. Accessed May 28, 2011.
    • (2011) FDA Label for EDURANTTM (Rilpivirine) Tablets
  • 8
    • 79960381844 scopus 로고    scopus 로고
    • Rilpivirine versus efavirenz with tenofovir and emtricitabine in treatment-naive adults infected with HIV-1 (ECHO): A phase 3 randomised double-blind activecontrolled trial
    • for the ECHO study group
    • Molina JM, Cahn P, Grinsztejn B, et al, for the ECHO study group. Rilpivirine versus efavirenz with tenofovir and emtricitabine in treatment-naive adults infected with HIV-1 (ECHO): a phase 3 randomised double-blind activecontrolled trial. Lancet 2011;378:238-246.
    • (2011) Lancet , vol.378 , pp. 238-246
    • Molina, J.M.1    Cahn, P.2    Grinsztejn, B.3
  • 9
    • 79960358849 scopus 로고    scopus 로고
    • Rilpivirine versus efavirenz with two background nucleoside or nucleotide reverse transcriptase inhibitors in treatment-naive adults infected with HIV-1 (THRIVE): A phase 3, randomised, non-inferiority trial
    • for the THRIVE study group
    • Cohen CJ, Andrade-Villanueva J, Clotet B, et al, for the THRIVE study group. Rilpivirine versus efavirenz with two background nucleoside or nucleotide reverse transcriptase inhibitors in treatment-naive adults infected with HIV-1 (THRIVE): a phase 3, randomised, non-inferiority trial. Lancet 2011;378:229-237.
    • (2011) Lancet , vol.378 , pp. 229-237
    • Cohen, C.J.1    Andrade-Villanueva, J.2    Clotet, B.3
  • 11
    • 73649148381 scopus 로고    scopus 로고
    • Efficacy and safety of TMC278 in antiretroviral-naive HIV-1 patients: Week 96 results of a Phase IIb randomized trial
    • Pozniak AL, Morales-Ramirez J, Katabira E, et al.: Efficacy and safety of TMC278 in antiretroviral-naive HIV-1 patients: Week 96 results of a Phase IIb randomized trial. AIDS 2010; 24:55-65.
    • (2010) AIDS , vol.24 , pp. 55-65
    • Pozniak, A.L.1    Morales-Ramirez, J.2    Katabira, E.3
  • 14
    • 77956089960 scopus 로고    scopus 로고
    • TMC278 25mg qd has no effect on corrected QT interval in a study in HIVnegative volunteers
    • Cologne Germany November [abstract PE7.1/2]
    • Vanveggel S, Buelens A, Crauwels HM, et al.: TMC278 25mg qd has no effect on corrected QT interval in a study in HIVnegative volunteers. 12th European AIDS Conference; Cologne, Germany, November 2009 [abstract PE7.1/2].
    • (2009) 12th European AIDS Conference
    • Vanveggel, S.1    Buelens, A.2    Crauwels, H.M.3
  • 17
    • 20444491186 scopus 로고    scopus 로고
    • Discordant conclusions from HIV clinical trials - An evaluation of efficacy endpoints
    • Hill A and DeMasi R: Discordant conclusions from HIV efficacy trials-an evaluation of efficacy endpoints. Antivir Ther 2005;10:367-374. (Pubitemid 41151015)
    • (2005) Antiviral Therapy , vol.10 , Issue.3 , pp. 367-374
    • Hill, A.1    DeMasi, R.2
  • 18
    • 84860474742 scopus 로고    scopus 로고
    • Genotypic and phenotypic characterization of HIV-1 isolates obtained from patients failing TMC278 in the phase 3 studies ECHO and THRIVE: 48-week analysis [Abstract 49
    • Rimsky L, Vingerhoets J and Van Eygen V, et al.: Genotypic and phenotypic characterization of HIV-1 isolates obtained from patients failing TMC278 in the phase 3 studies ECHO and THRIVE: 48-week analysis [Abstract 49]. Antivir Ther. 2011;16(Suppl 1):A17.
    • (2011) Antivir Ther. , vol.16 , Issue.SUPPL.1
    • Rimsky, L.1    Vingerhoets, J.2    Van Eygen, V.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.