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1
In vitro metabolism of canagliflozin in human liver, kidney, intestine microsomes, and recombinant uridine diphosphate glucuronosyltransferases (UGT) and the effect of genetic variability of UGT enzymes on the pharmacokinetics of canagliflozin in humans
In vitro metabolism of canagliflozin in human liver, kidney, intestine microsomes, and recombinant uridine diphosphate glucuronosyltransferases (UGT) and the effect of genetic variability of UGT enzymes on the pharmacokinetics of canagliflozin in humans
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In vitro metabolism of canagliflozin in human liver, kidney, intestine microsomes, and recombinant uridine diphosphate glucuronosyltransferases (UGT) and the effect of genetic variability of UGT enzymes on the pharmacokinetics of canagliflozin in humans

Francke, Stephan ; Mamidi, Rao N. V. S. ; Solanki, Bhavna ; Scheers, Ellen ; Jadwin, Andrew ; Favis, Reyna ; Devineni, Damayanthi

Journal of clinical pharmacology, 2015-09, Vol.55 (9), p.1061-1072 [Periódico revisado por pares]

England: Blackwell Publishing Ltd

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2
In vitro and physiologically‐based pharmacokinetic based assessment of drug–drug interaction potential of canagliflozin
In vitro and physiologically‐based pharmacokinetic based assessment of drug–drug interaction potential of canagliflozin
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In vitro and physiologically‐based pharmacokinetic based assessment of drug–drug interaction potential of canagliflozin

Mamidi, Rao N. V. S. ; Dallas, Shannon ; Sensenhauser, Carlo ; Lim, Heng Keang ; Scheers, Ellen ; Verboven, Peter ; Cuyckens, Filip ; Leclercq, Laurent ; Evans, David C. ; Kelley, Michael F. ; Johnson, Mark D. ; Snoeys, Jan

British journal of clinical pharmacology, 2017-05, Vol.83 (5), p.1082-1096 [Periódico revisado por pares]

England: John Wiley and Sons Inc

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3
Prediction of the drug–drug interaction potential of the α1‐acid glycoprotein bound, CYP3A4/CYP2C9 metabolized oncology drug, erdafitinib
Prediction of the drug–drug interaction potential of the α1‐acid glycoprotein bound, CYP3A4/CYP2C9 metabolized oncology drug, erdafitinib
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Prediction of the drug–drug interaction potential of the α1‐acid glycoprotein bound, CYP3A4/CYP2C9 metabolized oncology drug, erdafitinib

De Zwart, Loeckie ; Snoeys, Jan ; Jacobs, Frank ; Li, Lilian Y. ; Poggesi, Italo ; Verboven, Peter ; Goris, Ivo ; Scheers, Ellen ; Wynant, Inneke ; Monshouwer, Mario ; Mamidi, Rao N. V. S.

CPT: Pharmacometrics & Systems Pharmacology, 2021-09, Vol.10 (9), p.1107-1118 [Periódico revisado por pares]

United States: John Wiley & Sons, Inc

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4
Absolute oral bioavailability and pharmacokinetics of canagliflozin: A microdose study in healthy participants
Absolute oral bioavailability and pharmacokinetics of canagliflozin: A microdose study in healthy participants
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Absolute oral bioavailability and pharmacokinetics of canagliflozin: A microdose study in healthy participants

Devineni, Damayanthi ; Murphy, Joseph ; Wang, Shean-Sheng ; Stieltjes, Hans ; Rothenberg, Paul ; Scheers, Ellen ; Mamidi, Rao N.V.S.

Clinical pharmacology in drug development, 2015-07, Vol.4 (4), p.295-304 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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5
Effect of canagliflozin on the pharmacokinetics of glyburide, metformin, and simvastatin in healthy participants
Effect of canagliflozin on the pharmacokinetics of glyburide, metformin, and simvastatin in healthy participants
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Effect of canagliflozin on the pharmacokinetics of glyburide, metformin, and simvastatin in healthy participants

Devineni, Damayanthi ; Manitpisitkul, Prasarn ; Murphy, Joseph ; Skee, Donna ; Wajs, Ewa ; Mamidi, Rao N. V. S. ; Tian, Hong ; Vandebosch, An ; Wang, Shean-Sheng ; Verhaeghe, Tom ; Stieltjes, Hans ; Usiskin, Keith

Clinical pharmacology in drug development, 2015-05, Vol.4 (3), p.226-236 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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6
Safety, Tolerability, and Pharmacokinetics of a Capsule Formulation of DRF-1042, a Novel Camptothecin Analog, in Refractory Cancer Patients in a Bridging Phase I Study
Safety, Tolerability, and Pharmacokinetics of a Capsule Formulation of DRF-1042, a Novel Camptothecin Analog, in Refractory Cancer Patients in a Bridging Phase I Study
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Safety, Tolerability, and Pharmacokinetics of a Capsule Formulation of DRF-1042, a Novel Camptothecin Analog, in Refractory Cancer Patients in a Bridging Phase I Study

Chatterjee, Arani ; Digumarti, Raghunadharao ; Katneni, Kasiram ; Upreti, Vijay V. ; Mamidi, Rao N. V. S. ; Mullangi, Ramesh ; Surath, Anjna ; Srinivas, Maddali L. ; Uppalapati, Srihari ; Jiwatani, Sangeeta ; Srinivas, Nuggehally R.

Journal of clinical pharmacology, 2005-04, Vol.45 (4), p.453-460 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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7
Determination of lipoic acid in rat plasma by LC-MS/MS with electrospray ionization: Assay development, validation and application to a pharamcokinetic study
Determination of lipoic acid in rat plasma by LC-MS/MS with electrospray ionization: Assay development, validation and application to a pharamcokinetic study
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Determination of lipoic acid in rat plasma by LC-MS/MS with electrospray ionization: Assay development, validation and application to a pharamcokinetic study

Trivedi, Ravi Kumar ; Kallem, Raja Reddy ; Mamidi, Rao N. V. S. ; Mullangi, Ramesh ; Srinivas, Nuggehally R.

Biomedical chromatography, 2004-11, Vol.18 (9), p.681-686 [Periódico revisado por pares]

Chichester, UK: John Wiley & Sons, Ltd

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8
Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of an Orally Active Novel Camptothecin Analog, DRF-1042, in Refractory Cancer Patients in a Phase I Dose Escalation Study
Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of an Orally Active Novel Camptothecin Analog, DRF-1042, in Refractory Cancer Patients in a Phase I Dose Escalation Study
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Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of an Orally Active Novel Camptothecin Analog, DRF-1042, in Refractory Cancer Patients in a Phase I Dose Escalation Study

Chatterjee, Arani ; Digumarti, Raghunadharao ; Mamidi, Rao N. V. S. ; Katneni, Kasiram ; Upreti, Vijay V. ; Surath, Anjna ; Srinivas, Maddali L. ; Uppalapati, Srihari ; Jiwatani, Sangeeta ; Subramaniam, Swaminathan ; Srinivas, Nuggehally R.

Journal of clinical pharmacology, 2004-07, Vol.44 (7), p.723-736 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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9
Bioanalytical considerations for compounds containing free sulfhydryl groups
Bioanalytical considerations for compounds containing free sulfhydryl groups
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Bioanalytical considerations for compounds containing free sulfhydryl groups

Srinivas, Nuggehally R. ; Mamidi, Rao N. V. S.

Biomedical chromatography, 2003-07, Vol.17 (5), p.285-291 [Periódico revisado por pares]

Chichester, UK: John Wiley & Sons, Ltd

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10
Assessing the issue of instability due to Michael adduct formation in novel chemical entities possessing a carbon-carbon double bond during early drug development- applicability of common laboratory analytical protocols
Assessing the issue of instability due to Michael adduct formation in novel chemical entities possessing a carbon-carbon double bond during early drug development- applicability of common laboratory analytical protocols
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Assessing the issue of instability due to Michael adduct formation in novel chemical entities possessing a carbon-carbon double bond during early drug development- applicability of common laboratory analytical protocols

Polepally, Akshanth Reddy ; Kumar, Venkata V. Pavan ; Bhamidipati, Ravikanth ; Kota, Jagannath ; Naveed, Shaik Abdul ; Reddy, Karnati Harinder ; Mamidi, Rao N.V.S. ; Selvakumar, N. ; Mullangi, Ramesh ; Srinivas, Nuggehally R.

Biomedical chromatography, 2008-09, Vol.22 (9), p.960-976 [Periódico revisado por pares]

Chichester, UK: John Wiley & Sons, Ltd

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