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  1. Article ; Online: Using Mitra sampling to support first-in-human pharmacokinetic evaluations for PF-07059013.

    Lee, Kimberly C / Wan, Katty X / Barricklow, Jason / Lim, Chay Ngee / Clarke, Stephen / Potts, Daniel / Holmes, Kevin / Gonzalez, Pilar / Kavetska, Olga

    Bioanalysis

    2023  Volume 15, Issue 17, Page(s) 1083–1094

    Abstract: Aim: ...

    Abstract Aim:
    MeSH term(s) Humans ; Tandem Mass Spectrometry/methods ; Dried Blood Spot Testing/methods ; Specimen Handling ; Chromatography, High Pressure Liquid/methods ; Hematocrit
    Language English
    Publishing date 2023-08-16
    Publishing country England
    Document type Journal Article ; Review
    ISSN 1757-6199
    ISSN (online) 1757-6199
    DOI 10.4155/bio-2023-0066
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Effects of nirmatrelvir/ritonavir on midazolam and dabigatran pharmacokinetics in healthy participants.

    Cox, Donna S / Rehman, Muhammad / Khan, Tahira / Ginman, Katherine / Salageanu, Joanne / LaBadie, Robert R / Wan, Katty / Damle, Bharat

    British journal of clinical pharmacology

    2023  Volume 89, Issue 11, Page(s) 3352–3363

    Abstract: Aims: To evaluate pharmacokinetics (PK) and safety after coadministration of nirmatrelvir/ritonavir or ritonavir alone with midazolam (a cytochrome P450 3A4 substrate) and dabigatran (a P-glycoprotein substrate).: Methods: PK was studied in 2 phase 1, ...

    Abstract Aims: To evaluate pharmacokinetics (PK) and safety after coadministration of nirmatrelvir/ritonavir or ritonavir alone with midazolam (a cytochrome P450 3A4 substrate) and dabigatran (a P-glycoprotein substrate).
    Methods: PK was studied in 2 phase 1, open-label, fixed-sequence studies in healthy adults. Single oral doses of midazolam 2 mg (n = 12) or dabigatran 75 mg (n = 24) were administered alone and after steady state (i.e. ≥2 days) of nirmatrelvir/ritonavir 300 mg/100 mg and ritonavir 100 mg. Midazolam and dabigatran plasma concentrations and adverse events were analysed for each treatment.
    Results: After administration of midazolam with nirmatrelvir/ritonavir (test) or alone (reference), midazolam geometric mean area under the concentration-time curve extrapolated to infinity (AUC
    Conclusion: Coadministration of midazolam or dabigatran with nirmatrelvir/ritonavir increased systemic exposure of midazolam or dabigatran. Midazolam exposures were comparable when coadministered with nirmatrelvir/ritonavir or ritonavir alone, suggesting no incremental effect of nirmatrelvir. Dabigatran C
    MeSH term(s) Adult ; Humans ; Midazolam/pharmacokinetics ; Ritonavir ; Dabigatran/adverse effects ; Dabigatran/pharmacokinetics ; Healthy Volunteers ; Drug Interactions ; Area Under Curve ; Cytochrome P-450 CYP3A/metabolism
    Chemical Substances Midazolam (R60L0SM5BC) ; Ritonavir (O3J8G9O825) ; Dabigatran (I0VM4M70GC) ; Cytochrome P-450 CYP3A (EC 1.14.14.1)
    Language English
    Publishing date 2023-07-12
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 188974-6
    ISSN 1365-2125 ; 0306-5251 ; 0264-3774
    ISSN (online) 1365-2125
    ISSN 0306-5251 ; 0264-3774
    DOI 10.1111/bcp.15835
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Patient Centric Microsampling to Support Paxlovid Clinical Development: Bridging and Implementation.

    Wan, Katty / Kavetska, Olga / Damle, Bharat / Shi, Haihong / Cox, Donna S / Oladoyinbo, Olayide / Chan, Phylinda / Singh, Ravi Shankar P / Craft, Susan / Berthier, Erwin / Corrigan, Brian

    Clinical pharmacology and therapeutics

    2023  Volume 115, Issue 1, Page(s) 42–51

    Abstract: Nirmatrelvir is a potent and selective severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2) main protease inhibitor. Nirmatrelvir co-packaged with ritonavir (as PAXLOVID) received US Food and Drug Administration (FDA) Emergency Use Authorization ( ...

    Abstract Nirmatrelvir is a potent and selective severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2) main protease inhibitor. Nirmatrelvir co-packaged with ritonavir (as PAXLOVID) received US Food and Drug Administration (FDA) Emergency Use Authorization (EUA) on December 22, 2021, as an oral treatment for coronavirus disease 2019 (COVID-19) and subsequent new drug application approval on May 25, 2023. Pharmacokinetic (PK) capillary blood sampling at-home using Tasso-M20 micro-volumetric sampling device was implemented in the program, including three phase II/III outpatient and several clinical pharmacology studies supporting the EUA. The at-home sampling complemented venous blood sampling procedures to enrich the PK dataset, to decrease the need for patients' site visit for PK sampling, and to allow different sampling approaches for flexibility and convenience. To demonstrate concordance/equivalence, bridging between venous plasma and Tasso dried blood results was conducted by comparing concentrations and derived PK parameters from both sampling approaches. In addition, a two-compartment population PK model was utilized to bridge the plasma and Tasso data by estimating the PK parameters using blood-to-plasma ratio as a slope parameter. Operational challenges were successfully managed to implement at-home PK sampling in global phase II/III trials. Sample quality was generally very good with less than 3% samples deemed as "not usable" from over 800 samples collected in all the studies. Experience gained from sites and patients will guide future broader implementations.
    MeSH term(s) United States ; Humans ; Lactams ; Leucine ; Ritonavir ; Patient-Centered Care
    Chemical Substances nirmatrelvir and ritonavir drug combination ; Lactams ; Leucine (GMW67QNF9C) ; Ritonavir (O3J8G9O825)
    Language English
    Publishing date 2023-09-05
    Publishing country United States
    Document type Journal Article
    ZDB-ID 123793-7
    ISSN 1532-6535 ; 0009-9236
    ISSN (online) 1532-6535
    ISSN 0009-9236
    DOI 10.1002/cpt.3025
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  4. Article: Quantitative Determination of ABT-925 in Human Plasma by On-Line SPE and LC-MS/MS: Validation and Sample Analysis in Phase II Studies.

    Wan, Katty / Rieser, Matthew / El-Shourbagy, Tawakol

    Pharmaceutics

    2010  Volume 2, Issue 2, Page(s) 171–181

    Abstract: A fully automated 96-well On-Line Solid Phase Extraction (SPE) followed by High Performance Liquid Chromatography (HPLC)-Tandem Mass Spectrometric (MS/MS) method for the determination of ABT-925 (2-{3-[4-(2-tert-Butyl-6-trifluoromethyl-pyrimidin-4-yl)- ... ...

    Abstract A fully automated 96-well On-Line Solid Phase Extraction (SPE) followed by High Performance Liquid Chromatography (HPLC)-Tandem Mass Spectrometric (MS/MS) method for the determination of ABT-925 (2-{3-[4-(2-tert-Butyl-6-trifluoromethyl-pyrimidin-4-yl)-piperazin-1-yl)-propyl-sulfanyl}-3H-pyrimidin-4-one fumarate) in human plasma was developed, validated and utilized in Phase II clinical studies. 50 µL of plasma sample was fortified with internal standard (IS, d8-ABT-925) and extracted on-line with Cohesive Turbo Flow Cyclone P HTLC column. The chromatographic separation was performed on Aquasil C18 (3 μm 50 × 3 mm) HPLC column with a mobile phase consisting of 50/50/0.1 (v/v/v) ACN/H₂O/formic acid. The mass spectrometric measurement was conducted under positive ion mode using multiple reaction monitoring (MRM) of
    Language English
    Publishing date 2010-05-04
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2527217-2
    ISSN 1999-4923
    ISSN 1999-4923
    DOI 10.3390/pharmaceutics2020171
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Metabolism and Disposition of a Novel B-Cell Lymphoma-2 Inhibitor Venetoclax in Humans and Characterization of Its Unusual Metabolites.

    Liu, Hong / Michmerhuizen, Melissa J / Lao, Yanbin / Wan, Katty / Salem, Ahmed Hamed / Sawicki, James / Serby, Michael / Vaidyanathan, Srirajan / Wong, Shekman L / Agarwal, Suresh / Dunbar, Martin / Sydor, Jens / de Morais, Sonia M / Lee, Anthony J

    Drug metabolism and disposition: the biological fate of chemicals

    2017  Volume 45, Issue 3, Page(s) 294–305

    Abstract: Venetoclax (ABT-199), a B-cell lymphoma-2 (Bcl-2) protein inhibitor, is currently in clinical development for the treatment of hematologic malignancies. We characterized the absorption, metabolism, and excretion of venetoclax in humans. After a single ... ...

    Abstract Venetoclax (ABT-199), a B-cell lymphoma-2 (Bcl-2) protein inhibitor, is currently in clinical development for the treatment of hematologic malignancies. We characterized the absorption, metabolism, and excretion of venetoclax in humans. After a single oral dose of [
    Language English
    Publishing date 2017-03
    Publishing country United States
    Document type Journal Article
    ZDB-ID 186795-7
    ISSN 1521-009X ; 0090-9556
    ISSN (online) 1521-009X
    ISSN 0090-9556
    DOI 10.1124/dmd.116.071613
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Comparing similar spectra: from similarity index to spectral contrast angle.

    Wan, Katty X / Vidavsky, Ilan / Gross, Michael L

    Journal of the American Society for Mass Spectrometry

    2002  Volume 13, Issue 1, Page(s) 85–88

    Abstract: We investigated a spectral-contrast-angle (theta) method to determine whether mass spectra of structural isomers are the same or significantly different. This method represents collisionally activated dissociation (CAD) spectra as vectors in space. Mass ... ...

    Abstract We investigated a spectral-contrast-angle (theta) method to determine whether mass spectra of structural isomers are the same or significantly different. This method represents collisionally activated dissociation (CAD) spectra as vectors in space. Mass spectra of different isomers are represented as different vectors, having characteristic lengths and direction. The derived spectral contrast angle, which is a measure of the angle between two vectors corresponding to two closely related spectra, is a measure of whether the mass spectra are the same or significantly different. We compare this method with the similarity index (SI) method and show that the spectral contrast angle method is superior and can differentiate between very similar spectra in cases where the SI cannot. Both methods can be implemented simply in situations where the analyst is called on to decide, on the basis of mass or product-ion spectra, whether reference and unknown compounds are the same or to evaluate the reproducibility of spectra comprised of many peaks.
    MeSH term(s) Chemistry Techniques, Analytical/methods ; Oligodeoxyribonucleotides/chemistry ; Spectrometry, Mass, Electrospray Ionization/methods
    Chemical Substances Oligodeoxyribonucleotides
    Language English
    Publishing date 2002-01
    Publishing country United States
    Document type Comparative Study ; Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 1073671-2
    ISSN 1044-0305
    ISSN 1044-0305
    DOI 10.1016/S1044-0305(01)00327-0
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Toxicokinetic evaluation of atrasentan in mice utilizing serial microsampling: validation and sample analysis in GLP study.

    Wan, Katty X / Reimer, Michael T / Metchkarova, Maria P / Richter, Amy J / Paramadilok, Auratip / Kavetskaia, Olga / El-Shourbagy, Tawakol

    Bioanalysis

    2012  Volume 4, Issue 11, Page(s) 1351–1361

    Abstract: Background: A semi-automated 96-well protein precipitation followed by HPLC-MS/MS method for the determination of atrasentan (2R-[4-methoxyphenyl]-4S-[1,3-benzodioxol-5-yl]-1-[N,N-di-(N-butyl)-aminocarbonyl-methyl]-pyrrolidine-3R-carboxylic acid) in ... ...

    Abstract Background: A semi-automated 96-well protein precipitation followed by HPLC-MS/MS method for the determination of atrasentan (2R-[4-methoxyphenyl]-4S-[1,3-benzodioxol-5-yl]-1-[N,N-di-(N-butyl)-aminocarbonyl-methyl]-pyrrolidine-3R-carboxylic acid) in mouse whole blood was developed, validated and utilized in GLP toxicokinetic evaluations. Six 40-µl whole blood samples were collected from a single mouse over the course of a 12 h blood collection window. To avoid sample volume losses, whole blood was selected as the matrix in place of the more typically used plasma. A 10-µl assay volume was used to ensure sufficient volumes are available for dilutions, repeats and incurred sample reanalysis. The samples (10-µl aliquot) were fortified with stable-labeled internal standard (d18-atrasentan) and lysed thoroughly prior to protein precipitation. The chromatographic separation was performed on a Zorbax(®) SB-C18 (50 x 2.1 mm; 5 µm) HPLC column with a mobile phase consisting of 25 mM ammonium acetate and 0.25% (v/v) acetic acid in 50/50 (v/v) acetonitrile/water. The MS measurement was conducted under positive ion mode using multiple-reaction monitoring of m/z 511→354 for analyte and 529→354 for stable-labeled internal standard. The peak area ratio (analyte:stable-labeled internal standard) was used to quantitate atrasentan.
    Results: A dynamic range of 5-1400 ng/ml was established after validation. The challenges associated with a small-volume whole-blood assay involved anticoagulant overloading with commercial blood collection tubes, managing phospholipids to ensure a robust assay and automation. In-depth discussions are provided in this article. The validated method was then used for GLP toxicokinetic evaluations. To demonstrate the method reproducibility, approximately 10% of the incurred samples from the study were repeated in singlet. Excellent assay reproducibility was demonstrated where 100% of samples met incurred sample reanalysis acceptance criteria.
    Conclusion: Good quality exposure data were obtained from every serial sampled mouse in the study.
    MeSH term(s) Animals ; Chromatography, High Pressure Liquid/standards ; Male ; Mice ; Pharmacokinetics ; Phospholipids/chemistry ; Phospholipids/isolation & purification ; Pyrrolidines/blood ; Pyrrolidines/standards ; Quality Control ; Reference Standards ; Reproducibility of Results ; Tandem Mass Spectrometry/standards
    Chemical Substances Phospholipids ; Pyrrolidines ; atrasentan (V6D7VK2215)
    Language English
    Publishing date 2012-06
    Publishing country England
    Document type Evaluation Studies ; Journal Article ; Validation Studies
    ISSN 1757-6199
    ISSN (online) 1757-6199
    DOI 10.4155/bio.12.91
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  8. Article ; Online: 2022 White Paper on Recent Issues in Bioanalysis: ICH M10 BMV Guideline & Global Harmonization; Hybrid Assays; Oligonucleotides & ADC; Non-Liquid & Rare Matrices; Regulatory Inputs (

    Szapacs, Matt / Jian, Wenying / Spellman, Daniel / Cunliffe, Jennifer / Verburg, Elizabeth / Kaur, Surinder / Kellie, John / Li, Wenkui / Mehl, John / Qian, Mark / Qiu, Xiazi / Sirtori, Federico Riccardi / Rosenbaum, Anton I / Sikorski, Tim / Surapaneni, Sekhar / Wang, Jian / Wilson, Amanda / Zhang, Jinhui / Xue, Yongjun /
    Post, Noah / Huang, Yue / Goykhman, Dina / Yuan, Long / Fang, Kasie / Casavant, Ellen / Chen, Linzhi / Fu, Yunlin / Huang, Ming / Ji, Allena / Johnson, Jay / Lassman, Michael / Li, Jing / Saad, Ola / Sarvaiya, Hetal / Tao, Lin / Wang, Yuting / Zheng, Naiyu / Dasgupta, Arindam / Abhari, Mohsen Rajabi / Ishii-Watabe, Akiko / Saito, Yoshiro / Mendes Fernandes, Dulcyane Neiva / Bower, Joseph / Burns, Chris / Carleton, Kevin / Cho, Seongeun Julia / Du, Xiulian / Fjording, Marianne / Garofolo, Fabio / Kar, Sumit / Kavetska, Olga / Kossary, Elham / Lu, Yang / Mayer, Andrew / Palackal, Nisha / Salha, Danielle / Thomas, Eric / Verhaeghe, Tom / Vinter, Stephen / Wan, Katty / Wang, Yow-Ming / Williams, Kathi / Woolf, Eric / Yang, Li / Yang, Eric / Bandukwala, Abbas / Hopper, Shirley / Maher, Kevin / Xu, Joshua / Brodsky, Eric / Cludts, Isabelle / Irwin, Chad / Joseph, Julie / Kirshner, Susan / Manangeeswaran, Mohanraj / Maxfield, Kimberly / Pedras-Vasconcelos, Joao / Solstad, Therese / Thacker, Seth / Tounekti, Omar / Verthelyi, Daniela / Wadhwa, Meenu / Wagner, Leslie / Yamamoto, Takenori / Zhang, Lucia / Zhou, Lin

    Bioanalysis

    2023  Volume 15, Issue 16, Page(s) 955–1016

    Abstract: ... The ... ...

    Abstract The 16
    MeSH term(s) Chromatography ; Vaccines ; Biomarkers ; Cell- and Tissue-Based Therapy ; Mass Spectrometry ; Oligonucleotides ; Technology
    Chemical Substances Vaccines ; Biomarkers ; Oligonucleotides
    Language English
    Publishing date 2023-08-31
    Publishing country England
    Document type Journal Article
    ISSN 1757-6199
    ISSN (online) 1757-6199
    DOI 10.4155/bio-2023-0167
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: 2021 White Paper on Recent Issues in Bioanalysis: Mass Spec of Proteins, Extracellular Vesicles, CRISPR, Chiral Assays, Oligos; Nanomedicines Bioanalysis; ICH M10 Section 7.1; Non-Liquid & Rare Matrices; Regulatory Inputs (

    Kaur, Surinder / Alley, Stephen C / Szapacs, Matt / Wilson, Amanda / Ciccimaro, Eugene / Su, Dian / Henderson, Neil / Chen, Linzhi / Garofolo, Fabio / Hengel, Shawna / Jian, Wenying / Kellie, John F / Lee, Anita / Mehl, John / Palandra, Joe / Qiu, Haibo / Savoie, Natasha / Shakleya, Diaa / Staelens, Ludovicus /
    Sugimoto, Hiroshi / Sumner, Giane / Welink, Jan / Wheller, Robert / Xue, Y-J / Zeng, Jianing / Zhang, Jinhui / Zhou, Huiyu / Wang, Jian / Summerfield, Scott / Kavetska, Olga / Dillen, Lieve / Ramanathan, Ragu / Baratta, Mike / Dasgupta, Arindam / Edmison, Anna / Ferrari, Luca / Fischer, Sally / Fraier, Daniela / Haidar, Sam / Heermeier, Kathrin / James, Christopher / Ji, Allena / Luo, Lina / Lima Santos, Gustavo Mendes / Post, Noah / Rosenbaum, Anton I / Sporring, Sune / Surapaneni, Sekhar / Vinter, Stephen / Wan, Katty / Woolf, Eric / Cho, Seongeun Julia / Kossary, Elham / Prior, Sandra / Abhari, Mohsen Rajabi / Soo, Catherine / Wang, Yow-Ming / Bandukwala, Abbas / Cherry, Elana / Cludts, Isabelle / Ghosh, Soma / Hopper, Shirley / Ishii-Watabe, Akiko / Kirshner, Susan / Maher, Kevin / Maxfield, Kimberly / Pedras-Vasconcelos, Joao / Saito, Yoshiro / Smith, Dean / Solstad, Therese / Verthelyi, Daniela / Wadhwa, Meenu / Wagner, Leslie / Waxenecker, Günter / Yan, Haoheng / Zhang, Lucia

    Bioanalysis

    2022  Volume 14, Issue 9, Page(s) 505–580

    Abstract: The 15th edition of the Workshop on Recent Issues in Bioanalysis (15th WRIB) was held on 27 September to 1 October 2021. Even with a last-minute move from in-person to virtual, an overwhelmingly high number of nearly 900 professionals representing pharma ...

    Abstract The 15th edition of the Workshop on Recent Issues in Bioanalysis (15th WRIB) was held on 27 September to 1 October 2021. Even with a last-minute move from in-person to virtual, an overwhelmingly high number of nearly 900 professionals representing pharma and biotech companies, contract research organizations (CROs), and multiple regulatory agencies still eagerly convened to actively discuss the most current topics of interest in bioanalysis. The 15th WRIB included 3 Main Workshops and 7 Specialized Workshops that together spanned 1 week in order to allow exhaustive and thorough coverage of all major issues in bioanalysis, biomarkers, immunogenicity, gene therapy, cell therapy and vaccines. Moreover, in-depth workshops on biomarker assay development and validation (BAV) (focused on clarifying the confusion created by the increased use of the term "Context of Use - COU"); mass spectrometry of proteins (therapeutic, biomarker and transgene); state-of-the-art cytometry innovation and validation; and, critical reagent and positive control generation were the special features of the 15th edition. This 2021 White Paper encompasses recommendations emerging from the extensive discussions held during the workshop, and is aimed to provide the bioanalytical community with key information and practical solutions on topics and issues addressed, in an effort to enable advances in scientific excellence, improved quality and better regulatory compliance. Due to its length, the 2021 edition of this comprehensive White Paper has been divided into three parts for editorial reasons. This publication (Part 1A) covers the recommendations on Endogenous Compounds, Small Molecules, Complex Methods, Regulated Mass Spec of Large Molecules, Small Molecule, PoC. Part 1B covers the Regulatory Agencies' Inputs on Bioanalysis, Biomarkers, Immunogenicity, Gene & Cell Therapy and Vaccine. Part 2 (ISR for Biomarkers, Liquid Biopsies, Spectral Cytometry, Inhalation/Oral & Multispecific Biotherapeutics, Accuracy/LLOQ for Flow Cytometry) and Part 3 (TAb/NAb, Viral Vector CDx, Shedding Assays; CRISPR/Cas9 & CAR-T Immunogenicity; PCR & Vaccine Assay Performance; ADA Assay Comparabil ity & Cut Point Appropriateness) are published in volume 14 of Bioanalysis, issues 10 and 11 (2022), respectively.
    MeSH term(s) Biomarkers/analysis ; Cell- and Tissue-Based Therapy ; Extracellular Vesicles/chemistry ; Humans ; Mass Spectrometry/methods ; Nanomedicine ; Vaccines
    Chemical Substances Biomarkers ; Vaccines
    Language English
    Publishing date 2022-05-17
    Publishing country England
    Document type Journal Article
    ISSN 1757-6199
    ISSN (online) 1757-6199
    DOI 10.4155/bio-2022-0078
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  10. Article: ABT-335, the choline salt of fenofibric acid, does not have a clinically significant pharmacokinetic interaction with rosuvastatin in humans.

    Zhu, Tong / Awni, Walid M / Hosmane, Balakrishna / Kelly, Maureen T / Sleep, Darryl J / Stolzenbach, James C / Wan, Katty / Chira, Titus O / Pradhan, Rajendra S

    Journal of clinical pharmacology

    2009  Volume 49, Issue 1, Page(s) 63–71

    Abstract: ABT-335 is the choline salt of fenofibric acid under clinical development as a combination therapy with rosuvastatin for the management of dyslipidemia. ABT-335 and rosuvastatin have different mechanisms of actions and exert complementary pharmacodynamic ...

    Abstract ABT-335 is the choline salt of fenofibric acid under clinical development as a combination therapy with rosuvastatin for the management of dyslipidemia. ABT-335 and rosuvastatin have different mechanisms of actions and exert complementary pharmacodynamic effects on lipids. The current study assessed the pharmacokinetic interaction between the 2 drugs following a multiple-dose, open-label, 3-period, randomized, crossover design. Eighteen healthy men and women received 40 mg rosuvastatin alone, 135 mg ABT-335 alone, and the 2 drugs in combination once daily for 10 days. Blood samples were collected prior to dosing on multiple days and up to 120 hours after day 10 dosing for the measurements of fenofibric acid and rosuvastatin plasma concentrations. Coadministering 40 mg rosuvastatin had no significant effect on the steady-state Cmax, Cmin, or AUC24 of fenofibric acid (P > .05). Coadministering ABT-335 had no significant effect on the steady-state Cmin or AUC24 of rosuvastatin (P > .05) but increased Cmax by 20% (90% confidence interval: 12%-28%). All 3 regimens were generally well tolerated with no clinically significant changes in clinical laboratory values, vital signs, or electrocardiograms during the study. Results from this study demonstrate no clinically significant pharmacokinetic interaction between ABT-335 at the full clinical dose and rosuvastatin at the highest approved dose.
    MeSH term(s) Adult ; Cross-Over Studies ; Drug Interactions ; Female ; Fenofibrate/adverse effects ; Fenofibrate/analogs & derivatives ; Fenofibrate/blood ; Fenofibrate/pharmacokinetics ; Fluorobenzenes/adverse effects ; Fluorobenzenes/blood ; Fluorobenzenes/pharmacokinetics ; Humans ; Hypolipidemic Agents/adverse effects ; Hypolipidemic Agents/blood ; Hypolipidemic Agents/pharmacokinetics ; Male ; Middle Aged ; Pyrimidines/adverse effects ; Pyrimidines/blood ; Pyrimidines/pharmacokinetics ; Rosuvastatin Calcium ; Sulfonamides/adverse effects ; Sulfonamides/blood ; Sulfonamides/pharmacokinetics ; Young Adult
    Chemical Substances 2-(4-(4-chlorobenzoyl)phenoxy)-2-methylpropanoic acid ; Fluorobenzenes ; Hypolipidemic Agents ; Pyrimidines ; Sulfonamides ; Rosuvastatin Calcium (83MVU38M7Q) ; fenofibric acid (BGF9MN2HU1) ; Fenofibrate (U202363UOS)
    Language English
    Publishing date 2009-01
    Publishing country England
    Document type Clinical Trial, Phase I ; Journal Article ; Randomized Controlled Trial
    ZDB-ID 188980-1
    ISSN 1552-4604 ; 0091-2700 ; 0021-9754
    ISSN (online) 1552-4604
    ISSN 0091-2700 ; 0021-9754
    DOI 10.1177/0091270008325671
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