161 related articles for article (PubMed ID: 32104318)
1. Virtual population pharmacokinetic using physiologically based pharmacokinetic model for evaluating bioequivalence of oral lacidipine formulations in dogs.
Yang B; Wu C; Ji B; Wu M; He Z; Shang L; Sun J
Asian J Pharm Sci; 2017 Jan; 12(1):98-104. PubMed ID: 32104318
[TBL] [Abstract][Full Text] [Related]
2. In Vitro In Vivo Extrapolation and Bioequivalence Prediction for Immediate-Release Capsules of Cefadroxil Based on a Physiologically-Based Pharmacokinetic ACAT Model.
Rahim N; Naqvi SBS
AAPS PharmSciTech; 2024 May; 25(5):100. PubMed ID: 38714602
[TBL] [Abstract][Full Text] [Related]
3. Pharmacokinetic properties and bioequivalence of 2 formulations of valsartan 160-mg tablets: A randomized, single-dose, 2-period crossover study in healthy Korean male volunteers.
Kim JE; Ki MH; Yoon IS; Cho HJ; Kim RS; Tae Kim G; Kim DD
Clin Ther; 2014 Feb; 36(2):273-9. PubMed ID: 24529292
[TBL] [Abstract][Full Text] [Related]
4. Evaluation of the Impacts of Formulation Parameters on the Pharmacokinetics and Bioequivalence of Risperidone Orodispersible Film: a Physiologically Based Pharmacokinetic Modeling Approach.
Chen F; Liu H; Wang B; Yang Z; Chen Y; Yang L; Wang B; Jiao Z; Lin HS; Quan Y; Wang H; Xiang X
AAPS PharmSciTech; 2020 Aug; 21(7):245. PubMed ID: 32856178
[TBL] [Abstract][Full Text] [Related]
5. Virtual bioequivalence for achlorhydric subjects: The use of PBPK modelling to assess the formulation-dependent effect of achlorhydria.
Doki K; Darwich AS; Patel N; Rostami-Hodjegan A
Eur J Pharm Sci; 2017 Nov; 109():111-120. PubMed ID: 28774813
[TBL] [Abstract][Full Text] [Related]
6. Virtual Bioequivalence Assessment of Elagolix Formulations Using Physiologically Based Pharmacokinetic Modeling.
Mukherjee D; Chen MJ; Shao X; Ju TR; Shebley M; Marroum P
AAPS J; 2023 Mar; 25(3):30. PubMed ID: 36949256
[TBL] [Abstract][Full Text] [Related]
7. Bioequivalence study between two formulations of ciclosporin A (Cyclavance® oral solution and Atopica® soft capsules) following a single oral administration to dogs.
Navarro C; Séguy L; Vila M; Birckel P
BMC Vet Res; 2016 Mar; 12():54. PubMed ID: 26970736
[TBL] [Abstract][Full Text] [Related]
8. Establishing virtual bioequivalence and clinically relevant specifications using in vitro biorelevant dissolution testing and physiologically-based population pharmacokinetic modeling. case example: Naproxen.
Loisios-Konstantinidis I; Cristofoletti R; Fotaki N; Turner DB; Dressman J
Eur J Pharm Sci; 2020 Feb; 143():105170. PubMed ID: 31783158
[TBL] [Abstract][Full Text] [Related]
9. Bioequivalence of fixed dose combination of atorvastatin 10 mg and aspirin 150 mg capsules: a randomized, open-label, single-dose, two-way crossover study in healthy human subjects.
Tippabhotla SK; Betha MR; Gadiko C; Battula R; Nakkawar M; Cheerla R; Khan SM; Yergude S; Thota S; Vobalaboina V
Drug Res (Stuttg); 2013 May; 63(5):250-7. PubMed ID: 23526241
[TBL] [Abstract][Full Text] [Related]
10. Pharmacokinetics and bioequivalence evaluation of acamprosate calcium tablets in healthy Chinese volunteers.
Luo Z; Shen Y; Liang M; Miao J; Mei Y; Wang Y; Qin Y
Eur J Pharm Sci; 2015 Nov; 79():67-72. PubMed ID: 26360834
[TBL] [Abstract][Full Text] [Related]
11. Bioequivalence of two lansoprazole delayed release capsules 30 mg in healthy male volunteers under fasting, fed and fasting-applesauce conditions: a partial replicate crossover study design to estimate the pharmacokinetics of highly variable drugs.
Thota S; Khan SM; Tippabhotla SK; Battula R; Gadiko C; Vobalaboina V
Drug Res (Stuttg); 2013 Nov; 63(11):551-7. PubMed ID: 23780504
[TBL] [Abstract][Full Text] [Related]
12. Pharmacokinetics and bioequivalence of two oral formulations of canagliflozin after single-dose administration in healthy Chinese subjects
.
Hu W; Yang Y; Zhang Q; Yang Y; Zhou R; Lu C; Liu Z
Int J Clin Pharmacol Ther; 2020 Jan; 58(1):57-65. PubMed ID: 31347489
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Investigating the Impact of Drug Crystallinity in Amorphous Tacrolimus Capsules on Pharmacokinetics and Bioequivalence Using Discriminatory In Vitro Dissolution Testing and Physiologically Based Pharmacokinetic Modeling and Simulation.
Purohit HS; Trasi NS; Sun DD; Chow ECY; Wen H; Zhang X; Gao Y; Taylor LS
J Pharm Sci; 2018 May; 107(5):1330-1341. PubMed ID: 29289674
[TBL] [Abstract][Full Text] [Related]
15. Comparative pharmacokinetic and bioequivalence study of azithromycin 500 mg tablet in healthy Bangladeshi volunteers.
Ahmed MU; Islam MS; Shohag H; Karim R; Mostofa AG; Bhuiyan NH; Rahim M; Hasnat A
Int J Clin Pharmacol Ther; 2012 Jun; 50(6):452-8. PubMed ID: 22677307
[TBL] [Abstract][Full Text] [Related]
16. Bioequivalence and pharmacokinetic evaluation of two tablet formulations of carvedilol 25-mg: a single-dose, randomized-sequence, open-label, two-way crossover study in healthy Chinese male volunteers.
Liu Y; Lu C; Chen Q; Wang W; Liu GY; Lu XP; Zhang MQ; Yu C; Jia JY
Drug Res (Stuttg); 2013 Feb; 63(2):74-8. PubMed ID: 23447077
[TBL] [Abstract][Full Text] [Related]
17. A Pharmacokinetic Bioequivalence Study Comparing Pirfenidone Tablet and Capsule Dosage Forms in Healthy Adult Volunteers.
Pan L; Belloni P; Ding HT; Wang J; Rubino CM; Putnam WS
Adv Ther; 2017 Sep; 34(9):2071-2082. PubMed ID: 28808905
[TBL] [Abstract][Full Text] [Related]
18. In vivo pharmacokinetic-pharmacodynamic relationship and in vitro equivalence of two oral furosemide tablet formulations.
Cuadrado A; Rodríguez Gascón A; Hernández RM; Castilla AM; de la Maza A; Yánez C; López de Ocáriz A; Solinís MA; Pedraz JL
Arzneimittelforschung; 2003; 53(5):321-9. PubMed ID: 12854359
[TBL] [Abstract][Full Text] [Related]
19. Bioequivalence Comparison of Pediatric Dasatinib Formulations and Elucidation of Absorption Mechanisms Through Integrated PBPK Modeling.
Vaidhyanathan S; Wang X; Crison J; Varia S; Gao JZH; Saxena A; Good D
J Pharm Sci; 2019 Jan; 108(1):741-749. PubMed ID: 30439460
[TBL] [Abstract][Full Text] [Related]
20. Bioequivalence study of two commercial amoxicillin suspension formulations in healthy human volunteers.
Franco GC; Baglie S; Ruenis AP; Franco LM; Cogo K; Oshima-Franco Y; Silva P; Groppo FC; Rosalen PL
Int J Clin Pharmacol Ther; 2014 May; 52(5):425-30. PubMed ID: 24755132
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
