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 *

180 related articles for article (PubMed ID: 34167827)

  • 41. Comparative steady-state pharmacokinetic evaluation of immediate-release topiramate and USL255, a once-daily extended-release topiramate formulation.
    Bialer M; Shekh-Ahmad T; Braun TL; Halvorsen MB
    Epilepsia; 2013 Aug; 54(8):1444-52. PubMed ID: 23692553
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Relative Oral Bioavailability of an Abuse-deterrent, Extended-release Formulation of Morphine Versus Extended-release Morphine: A 2-period, Single-dose, Randomized Crossover Study in Healthy Subjects.
    Kinzler ER; Pantaleon C; Aigner S
    Clin Ther; 2018 Aug; 40(8):1357-1365. PubMed ID: 30049503
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Pharmacokinetic properties of single- and repeated-dose sufentanil sublingual tablets in healthy volunteers.
    Willsie SK; Evashenk MA; Hamel LG; Hwang SS; Chiang YK; Palmer PP
    Clin Ther; 2015 Jan; 37(1):145-55. PubMed ID: 25544247
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Pharmacokinetic and safety profile of rupatadine when coadministered with azithromycin at steady-state levels: a randomized, open-label, two-way, crossover, Phase I study.
    Solans A; Izquierdo I; Donado E; Antonijoan R; Peña J; Nadal T; Carbó ML; Merlos M; Barbanoj M
    Clin Ther; 2008 Sep; 30(9):1639-50. PubMed ID: 18840369
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Single-dose bioequivalence assessment of two formulations of polysaccharide iron complex capsules in healthy adult male Chinese volunteers: A sequence-randomized, double-blind, two-way crossover study.
    Zhang YY; Liu JH; Su F; Lui YT; Li JF
    Curr Ther Res Clin Exp; 2009 Apr; 70(2):104-15. PubMed ID: 24683222
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Bioequivalence evaluation of single doses of two tramadol formulations: a randomized, open-label, two-period crossover study in healthy Brazilian volunteers.
    Silva Mde F; Schramm SG; Kano EK; Mori Koono EE; Porta V; dos Reis Serra CH
    Clin Ther; 2010 Apr; 32(4):758-65. PubMed ID: 20435245
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Bioequivalence assessment of two transdermal delivery systems of fentanyl in healthy Chinese volunteers.
    Liu J; Zhou X
    Int J Clin Pharmacol Ther; 2014 Feb; 52(2):175-80. PubMed ID: 24424109
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Comparative Bioavailability Study of a New Orodispersible Formulation of Ibuprofen Versus Two Existing Oral Tablet Formulations in Healthy Male and Female Volunteers.
    Sugár D; Francombe D; da Silva T; Hanid S; Hutchings S
    Clin Ther; 2019 Aug; 41(8):1486-1498. PubMed ID: 31202508
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Co-crystal of tramadol-celecoxib (CTC) for acute moderate-to-severe pain.
    Langford R; Margarit C; Morte A; Cebrecos J; Sust M; Ortiz E; Giménez-Arnau JM; de Leon-Casasola O
    Curr Med Res Opin; 2024 Mar; 40(3):455-468. PubMed ID: 38205948
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Celecoxib-tramadol co-crystal in patients with moderate-to-severe pain following bunionectomy with osteotomy: Secondary analyses by baseline pain intensity and use of rescue medication of a phase 3, randomized, double-blind, factorial, active- and placebo-controlled trial.
    Viscusi ER; de Leon-Casasola O; Cebrecos J; Jacobs A; Morte A; Ortiz E; Sust M; Vaqué A; Gottlieb I; Daniels S; Muse D; Kuss ME; Videla S; Gascón N; Plata-Salamán C
    Pain Pract; 2024 Jul; ():. PubMed ID: 38956758
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Pharmacokinetics and bioavailability of single dose ibuprofen and pseudoephedrine alone or in combination: a randomized three-period, cross-over trial in healthy Indian volunteers.
    Kale P
    Front Pharmacol; 2014; 5():98. PubMed ID: 24847268
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Pharmacokinetics of oral pridinol: Results of a randomized, crossover bioequivalence trial in healthy subjects.
    Richter M; Donath F; Wedemeyer RS; Warnke A; Horstmann A; Peschel C
    Int J Clin Pharmacol Ther; 2021 Jun; 59(6):471-477. PubMed ID: 33835016
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Influence of age on the pharmacokinetics of naftidrofuryl after single oral administration in elderly versus young healthy volunteers.
    Hulot T; Gamand S; Dupain T; Ahtoy P; Bromet M
    Arzneimittelforschung; 1998 Sep; 48(9):900-4. PubMed ID: 9793615
    [TBL] [Abstract][Full Text] [Related]  

  • 54. A Randomized Phase 1 Pharmacokinetic Study Comparing the Potential Biosimilar LRG201902 With Liraglutide (Victoza
    Mai G; Fan L; Li M; Zhang P; Gan C; Huang Q; Shentu J
    Front Pharmacol; 2020; 11():610880. PubMed ID: 33584289
    [No Abstract]   [Full Text] [Related]  

  • 55. 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; 89 Suppl 3():S79-85. PubMed ID: 17722305
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Comparative bioavailability of two tablet formulations of ranitidine hydrochloride in healthy volunteers.
    Bawazir SA; Gouda MW; El-Sayed YM; Al-Khamis KI; Al-Yamani MJ; Niazy EM; Al-Rashood KA
    Int J Clin Pharmacol Ther; 1998 May; 36(5):270-4. PubMed ID: 9629991
    [TBL] [Abstract][Full Text] [Related]  

  • 57. 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]  

  • 58. Pharmacokinetics and bioequivalence of single dose and multiple doses of immediate- and extended-release formulations of dexibuprofen in healthy Chinese subjects.
    Xu MJ; Zou C; H Chu J; Wu T; Liu SJ; Zhang J; Chen M; Liu F; Xiong NN; Ju WZ; S Tan H
    Int J Clin Pharmacol Ther; 2011 Mar; 49(3):237-46. PubMed ID: 21329626
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Comparative bioavailability of two tablet formulations of acyclovir in healthy volunteers.
    Al-Yamani MJ; Al-Khamis KI; El-Sayed YM; Bawazir SA; Al-Rashood KA; Gouda MW
    Int J Clin Pharmacol Ther; 1998 Apr; 36(4):222-6. PubMed ID: 9587049
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Comparison of the pharmacokinetics and tolerability of HCP1004 (a fixed-dose combination of naproxen and esomeprazole strontium) and VIMOVO® (a marketed fixed-dose combination of naproxen and esomeprazole magnesium) in healthy volunteers.
    Choi Y; Han H; Shin D; Lim KS; Yu KS
    Drug Des Devel Ther; 2015; 9():4127-35. PubMed ID: 26257511
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.