These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

90 related articles for article (PubMed ID: 26086613)

  • 1. Effect of Truncating AUC at 12, 24 and 48 hr When Evaluating the Bioequivalence of Drugs with a Long Half-Life.
    Moreno I; Ochoa D; Román M; Cabaleiro T; Abad-Santos F
    Basic Clin Pharmacol Toxicol; 2016 Jan; 118(1):53-7. PubMed ID: 26086613
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Truncated AUCs in the assessment of the bioequivalence of topiramate, a long half-life drug.
    Almeida S; Spínola AC; Filipe A; Trabelsi F; Farré A
    Arzneimittelforschung; 2007; 57(5):249-53. PubMed ID: 17598694
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A single-dose, randomized, two-way crossover study comparing two olanzapine tablet products in healthy adult male volunteers under fasting conditions.
    Elshafeey AH; Elsherbiny MA; Fathallah MM
    Clin Ther; 2009 Mar; 31(3):600-8. PubMed ID: 19393850
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Impact of Truncated Area on Point Estimate and Intra-Subject Variability in Bioequivalence of Dutasteride with Long Half-Life.
    Prasaja B; Harahap Y; Lusthom W; Yumi L; Sofiana A; Sandra M; Safira F; Chilmi U
    Drug Res (Stuttg); 2018 Apr; 68(4):238-240. PubMed ID: 29156456
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Truncated areas under the curve in the assessment of pioglitazone bioequivalence. Data from a single-center, single-dose, randomized, open-label, 2-way cross-over bioequivalence study of two formulations of pioglitazone 45 mg tablets under fasting conditions.
    Almeida S; Filipe A; Neves R; Pinho C; Pedroso P; Castillo A; Trabelsi F
    Arzneimittelforschung; 2011; 61(1):32-9. PubMed ID: 21355444
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Pharmacokinetics and bioequivalence study of irbesartan tablets after a single oral dose of 300 mg in healthy Thai volunteers.
    Wittayalertpanya S; Chariyavilaskul P; Prompila N; Sayankuldilok N; Eiamart W
    Int J Clin Pharmacol Ther; 2014 May; 52(5):431-6. PubMed ID: 24725445
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Bioequivalence study of two different tablet formulations of donepezil using truncated areas under the curve. A single-center, single-dose, randomized, open-label, 2-way crossover study under fasting conditions.
    Almeida S; Filipe A; Neves R; Desjardins I; Shink E; Castillo A
    Arzneimittelforschung; 2010; 60(3):116-23. PubMed ID: 20422942
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Utility of Pilot Studies for Predicting Ratios and Intrasubject Variability in High-Variability Drugs.
    Moreno I; Ochoa D; Román M; Cabaleiro T; Abad-Santos F
    Basic Clin Pharmacol Toxicol; 2016 Aug; 119(2):215-21. PubMed ID: 26806812
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Bioequivalence study of montelukast tablets in healthy Pakistani volunteers.
    Abbas M; Khan AM; Amin S; Riffat S; Ashraf M; Waheed N
    Pak J Pharm Sci; 2013 Mar; 26(2):255-9. PubMed ID: 23455193
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Impact of truncated area under the curve on failed bioequivalence studies: a computer simulation analysis.
    Mahmood I
    Drug Metabol Drug Interact; 2004; 20(1-2):77-83. PubMed ID: 15283304
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Experimental, extrapolated and truncated areas under the concentration-time curve in bioequivalence trials.
    Marzo A; Monti NC; Vuksic D
    Eur J Clin Pharmacol; 1999 Nov; 55(9):627-31. PubMed ID: 10638390
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Comparative bioavailability and pharmacokinetic study of Cefadroxil capsules in male healthy volunteers of Pakistan.
    Rahim N; Naqvi SB; Alam M; Rasheed A; Khalique UA
    Pak J Pharm Sci; 2016 Mar; 29(2):453-9. PubMed ID: 27087092
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Bioequivalence assessment of Lovrak (Julphar, UAE) compared with Zovirax (Glaxo Wellcome, UK)--Two brands of Acyclovir--in healthy human volunteers.
    Najib NM; Idkaidek N; Beshtawi M; Mohammed B; Admour I; Alam SM; Dham R;
    Biopharm Drug Dispos; 2005 Jan; 26(1):7-12. PubMed ID: 15578768
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mycophenolate mofetil 500-mg tablet under fasting conditions: single-dose, randomized-sequence, open-label, four-way replicate crossover, bioequivalence study in healthy subjects.
    Almeida S; Filipe A; Neves R; Spínola AC; Tanguay M; Ortuño J; Farré A; Torns A
    Clin Ther; 2010 Mar; 32(3):556-74. PubMed ID: 20399993
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Metronidazole immediate release formulations: a fasting randomized open-label crossover bioequivalence study in healthy volunteers.
    de Freitas Silva M; Schramm SG; Kano EK; Koono EE; Manfio JL; Porta V; dos Reis Serra CH
    Arzneimittelforschung; 2012 Oct; 62(10):490-5. PubMed ID: 22918856
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Investigation of bioequivalence of a new fixed-dose combination of acarbose and metformin with the corresponding loose combination as well as the drug-drug interaction potential between both drugs in healthy adult male subjects.
    Kim S; Jang IJ; Shin D; Shin DS; Yoon S; Lim KS; Yu KS; Li J; Zhang H; Liu Y; Brendel E; Blode H; Wang Y
    J Clin Pharm Ther; 2014 Aug; 39(4):424-31. PubMed ID: 24806030
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 30(10):1831-43. PubMed ID: 19014838
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Pharmacokinetics and bioequivalence evaluation of 2 levosulpiride preparations after a single oral dose in healthy male Korean volunteers.
    Cho HY; Moon JD; Lee YB
    Int J Clin Pharmacol Ther; 2004 Mar; 42(3):174-80. PubMed ID: 15049438
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A limited sampling approach in bioequivalence studies: application to long half-life drugs and replicate design studies.
    Mahmood I; Mahayni H
    Int J Clin Pharmacol Ther; 1999 Jun; 37(6):275-81. PubMed ID: 10395118
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Bioequivalence of Intravenous and Oral Rolapitant: Results From a Randomized, Open-Label Pivotal Study.
    Wang X; Zhang ZY; Powers D; Wang J; Lu S; Arora S; Hughes L; Christensen J; Kansra V
    J Clin Pharmacol; 2017 Dec; 57(12):1600-1606. PubMed ID: 28906561
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.