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Journal Abstract Search

74 related items for PubMed ID: 15907596

  • 1. Determination of lamivudine in human plasma by HPLC and its use in bioequivalence studies.
    Kano EK, dos Reis Serra CH, Koono EE, Andrade SS, Porta V.
    Int J Pharm; 2005 Jun 13; 297(1-2):73-9. PubMed ID: 15907596
    [Abstract] [Full Text] [Related]

  • 2. Bioequivalence assay between orally disintegrating and conventional tablet formulations in healthy volunteers.
    Armando YP, Schramm SG, Silva Mde F, Kano EK, Koono EE, Porta V, Serra CH.
    Int J Pharm; 2009 Jan 21; 366(1-2):149-53. PubMed ID: 18848869
    [Abstract] [Full Text] [Related]

  • 3. Bioequivalence and pharmacokinetics of two zidovudine formulations in healthy Brazilian volunteers: an open-label, randomized, single-dose, two-way crossover study.
    Dos Reis Serra CH, Mori Koono EE, Kano EK, Schramm SG, Armando YP, Porta V.
    Clin Ther; 2008 May 21; 30(5):902-8. PubMed ID: 18555936
    [Abstract] [Full Text] [Related]

  • 4. A single-dose, randomized, open-label, two-period crossover bioequivalence study of a fixed-dose pediatric combination of lamivudine 40-mg, nevirapine 70-mg, and stavudine 10-mg tablet for oral suspension with individual liquid formulations in healthy adult male volunteers.
    Monif T, Rao Thudi N, Koundinya Tippabhotla S, Khuroo A, Marwah A, Kumar Shrivastav V, Tandon M, Raghuvanshi R, Biswal S.
    Clin Ther; 2007 Dec 21; 29(12):2677-84. PubMed ID: 18201583
    [Abstract] [Full Text] [Related]

  • 5. Bioequivalence of two lamivudine tablet formulations.
    Santos-Magalhães NS, Pontes A, Cavalcante RM, Costa RM, Rangel FA, Guimarães MI, de Carvalho JN, de Souza SD, de Oliveira HM, Esteves IL, Ramalho MS, Vieira SL, Alves AJ.
    Arzneimittelforschung; 2001 Dec 21; 51(4):310-4. PubMed ID: 11367872
    [Abstract] [Full Text] [Related]

  • 6. Determination of stavudine in human serum by on-line solid-phase extraction coupled to high-performance liquid chromatography with electrospray ionization tandem mass spectrometry: application to a bioequivalence study.
    Raices RS, Salvadori MC, de Cassia E Estrela R, de Aquino Neto FR, Suarez-Kurtz G.
    Rapid Commun Mass Spectrom; 2003 Dec 21; 17(14):1611-8. PubMed ID: 12845587
    [Abstract] [Full Text] [Related]

  • 7. A combined-formulation tablet of lamivudine/nevirapine/stavudine: bioequivalence compared with concurrent administration of lamivudine, nevirapine, and stavudine in healthy Indian subjects.
    Narang VS, Lulla A, Malhotra G, Purandare S.
    J Clin Pharmacol; 2005 Mar 21; 45(3):265-74. PubMed ID: 15703362
    [Abstract] [Full Text] [Related]

  • 8. Evaluation of the bioequivalence of zidovudine 100 mg capsules in healthy Thai male volunteers.
    Chompootaweep S, Poonsrisawat J, Xumseang P.
    J Med Assoc Thai; 2006 Sep 21; 89 Suppl 3():S79-85. PubMed ID: 17722305
    [Abstract] [Full Text] [Related]

  • 9. A single-dose, randomized, open-label, two-period crossover bioequivalence study comparing a fixed-dose pediatric combination of lamivudine and stavudine tablet for oral suspension with individual liquid formulations in healthy adult male volunteers.
    Monif T, Reyar S, Tiwari HK, Tippabhotla SK, Khuroo A, Thudi NR, Ahmed S, Raghuvanshi R.
    Arzneimittelforschung; 2009 Sep 21; 59(2):104-8. PubMed ID: 19338141
    [Abstract] [Full Text] [Related]

  • 10. Pharmacokinetic comparison of generic and trade formulations of lamivudine, stavudine and nevirapine in HIV-infected Malawian adults.
    Hosseinipour MC, Corbett AH, Kanyama C, Mshali I, Phakati S, Rezk NL, van der Horst C, Kashuba AD.
    AIDS; 2007 Jan 02; 21(1):59-64. PubMed ID: 17148968
    [Abstract] [Full Text] [Related]

  • 11. Evaluation of the bioequivalence of capsules containing 150 mg of fluconazole.
    Porta V, Chang KH, Storpirtis S.
    Int J Pharm; 2005 Jan 06; 288(1):81-6. PubMed ID: 15607260
    [Abstract] [Full Text] [Related]

  • 12. Determination of nifedipine in human plasma and its use in bioequivalence study.
    Guo Y, Dai J, Qian G, Guo N, Ma Z, Guo X.
    Int J Pharm; 2007 Aug 16; 341(1-2):91-6. PubMed ID: 17507190
    [Abstract] [Full Text] [Related]

  • 13. Determination of secnidazole in human plasma by high-performance liquid chromatography with UV detection and its application to the bioequivalence studies.
    Li X, Sun J, Wang G, Zheng Y, Yan B, Xie H, Gu Y, Ren H.
    Biomed Chromatogr; 2007 Mar 16; 21(3):304-9. PubMed ID: 17221933
    [Abstract] [Full Text] [Related]

  • 14. Bioequivalence evaluation of a fixed dose combination lamivudine + stavudine tablet with concurrent administration of lamivudine tablet and stavudine capsule in healthy volunteers.
    Chachad S, Lulla A, Malhotra G, Purandare S.
    Arzneimittelforschung; 2009 Mar 16; 59(10):537-40. PubMed ID: 19998583
    [Abstract] [Full Text] [Related]

  • 15. A rapid and sensitive method for simultaneous determination of lamivudine and zidovudine in human serum by on-line solid-phase extraction coupled to liquid chromatography/tandem mass spectrometry detection.
    Estrela Rde C, Salvadori MC, Suarez-Kurtz G.
    Rapid Commun Mass Spectrom; 2004 Mar 16; 18(10):1147-55. PubMed ID: 15150840
    [Abstract] [Full Text] [Related]

  • 16. High-performance liquid chromatographic determination of lamivudine in human serum using liquid-liquid extraction; application to pharmacokinetic studies.
    Bahrami G, Mirzaeei S, Kiani A, Mohammadi B.
    J Chromatogr B Analyt Technol Biomed Life Sci; 2005 Sep 05; 823(2):213-7. PubMed ID: 16046202
    [Abstract] [Full Text] [Related]

  • 17. Simultaneous determination of stavudine and lamivudine in human plasma by high performance liquid chromatography and its application to a bioavailability study.
    Wattananat T, Prasanchaimontri IO, Akarawut W.
    Southeast Asian J Trop Med Public Health; 2010 Mar 05; 41(2):369-77. PubMed ID: 20578520
    [Abstract] [Full Text] [Related]

  • 18. Assessment of the bioequivalence of two formulations of clarithromycin extended-release 500-mg tablets under fasting and fed conditions: a single-dose, randomized, open-label, two-period, two-way crossover study in healthy Jordanian male volunteers.
    Alkhalidi BA, Tamimi JJ, Salem II, Ibrahim H, Sallam AA.
    Clin Ther; 2008 Oct 05; 30(10):1831-43. PubMed ID: 19014838
    [Abstract] [Full Text] [Related]

  • 19. Bioavailability and bioequivalence of two oral formulations of alendronate sodium 70 mg: an open-label, randomized, two-period crossover comparison in healthy Korean adult male volunteers.
    Rhim SY, Park JH, Park YS, Lee MH, Kim DS, Shaw LM, Yang SC, Kang JS.
    Clin Ther; 2009 May 05; 31(5):1037-45. PubMed ID: 19539104
    [Abstract] [Full Text] [Related]

  • 20. Saquinavir 500 mg film-coated tablets demonstrate bioequivalence to saquinavir 200 mg hard capsules when boosted with twice-daily ritonavir in healthy volunteers.
    Bittner B, Riek M, Holmes B, Grange S.
    Antivir Ther; 2005 May 05; 10(7):803-10. PubMed ID: 16312177
    [Abstract] [Full Text] [Related]

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