Search Results - "Mendonza, Anisha"
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The effects of licogliflozin, a dual SGLT1/2 inhibitor, on body weight in obese patients with or without diabetes
Published in Diabetes, obesity & metabolism (01-06-2019)“…BACKGROUND There is an unmet need for a safer and more effective treatment for obesity. This study assessed the effects of licogliflozin, a dual inhibitor of…”
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Investigation and Management of Stool Frequency and Consistency Associated With SGLT1 Inhibition by Reducing Dietary Carbohydrate: A Randomized Trial
Published in Clinical pharmacology and therapeutics (01-11-2020)“…Treatment with licogliflozin, a dual sodium‐glucose co‐transporter (SGLT)1/2‐inhibitor, is associated with increased stool frequency and loose stools,…”
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Licogliflozin for nonalcoholic steatohepatitis: a randomized, double-blind, placebo-controlled, phase 2a study
Published in Nature medicine (01-07-2022)“…Nonalcoholic steatohepatitis (NASH) is a common chronic liver disease that may advance to fibrosis and lead to mortality; however, no pharmacotherapy is…”
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Pharmacokinetics, metabolism, and excretion of licogliflozin, a dual inhibitor of SGLT1/2, in rats, dogs, and humans
Published in Xenobiotica (03-04-2021)“…Absorption, metabolism, and excretion (AME) of licogliflozin, a sodium-glucose co-transporters (SGLTs) 1 and 2 inhibitor, were studied in male rats, dogs, and…”
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Glucosuric, renal and haemodynamic effects of licogliflozin, a dual inhibitor of sodium‐glucose co‐transporter‐1 and sodium‐glucose co‐transporter‐2, in patients with chronic kidney disease: A randomized trial
Published in Diabetes, obesity & metabolism (01-05-2021)“…Aim To investigate the glucosuric, renal and haemodynamic effects of licogliflozin, a dual sodium‐glucose co‐transporter‐1 and sodium‐glucose co‐transporter‐2…”
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Pharmacokinetics, pharmacodynamics, safety, and efficacy of crizanlizumab in patients with sickle cell disease: final results from the phase II SOLACE-adults study
Published in Therapeutic advances in hematology (01-01-2024)“…Background: Crizanlizumab is a novel inhibitor of P-selectin, a key player in multicellular adhesion and inflammatory signaling, that leads to vaso-occlusion…”
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Evaluation of safety and tolerability, pharmacokinetics, and pharmacodynamics of BMS-820836 in healthy subjects: a placebo-controlled, ascending single-dose study
Published in Psychopharmacology (01-06-2014)“…Rationale BMS-820836, a novel triple monoamine reuptake inhibitor, is an experimental monotherapy for sufferers of major depressive disorder who have had an…”
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Ocular Pharmacology and Toxicology of TRPV1 Antagonist SAF312 (Libvatrep)
Published in Translational vision science & technology (01-09-2023)“…PurposeTo evaluate the pharmacology and toxicology of SAF312, a transient receptor potential vanilloid 1 (TRPV1) antagonist. MethodsTRPV1 expression in human…”
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The Concentration of Cyclosporine Metabolites Is Significantly Lower in Kidney Transplant Recipients With Diabetes Mellitus
Published in Therapeutic drug monitoring (01-02-2012)“…Diabetes mellitus is prevalent among kidney transplant recipients. The activity of drug metabolizing enzymes or transporters may be altered by diabetes leading…”
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Blood and Plasma Pharmacokinetics of Ciclosporin in Diabetic Kidney Transplant Recipients
Published in Clinical pharmacokinetics (01-01-2008)“…Background and objectives: Long-term diabetes mellitus may affect the absorption, distribution and metabolism of immunosuppressive agents used after organ…”
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Analysis of mycophenolic acid in saliva using liquid chromatography tandem mass spectrometry
Published in Therapeutic drug monitoring (01-06-2006)“…Salivary levels of the immunosuppressive agent, mycophenolic acid (MPA), may provide a convenient and noninvasive method for drug monitoring. An analytical…”
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Determination of total mycophenolic acid and its glucuronide metabolite using liquid chromatography with ultraviolet detection and unbound mycophenolic acid using tandem mass spectrometry
Published in Journal of chromatography. B, Analytical technologies in the biomedical and life sciences (25-12-2004)“…Two simple, sensitive and reproducible methods for determination of total mycophenolic acid (MPA) and its glucuronide metabolite (MPAG) as well as unbound MPA…”
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Tacrolimus in diabetic kidney transplant recipients : Pharmacokinetics and application of a limited sampling strategy
Published in Therapeutic drug monitoring (01-08-2007)“…The effect of diabetes mellitus on the pharmacokinetics of tacrolimus is not well characterized. We have compared tacrolimus 12-hour steady-state…”
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Bioavailability of valsartan oral dosage forms
Published in Clinical pharmacology in drug development (01-03-2014)“…The oral bioavailability of valsartan from extemporaneous suspension and solution formulations were evaluated relative to tablet formulation in two separate…”
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Pharmacokinetics, Pharmacodynamics, Safety, and Efficacy of Crizanlizumab in Patients with Sickle Cell Disease: Final Interim Analysis Results from the Phase 2 Solace-Adults Study
Published in Blood (02-11-2023)“…Background: Acute painful vaso-occlusive crises (VOCs), the hallmark of sickle cell disease (SCD), are associated with chronic and potentially life-threatening…”
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Assessment of pharmacokinetic drug-drug interaction between pradigastat and atazanavir or probenecid
Published in Journal of clinical pharmacology (01-03-2016)“…Pradigastat, a novel diacylglycerol acyltransferase‐1 inhibitor, has activity in common metabolic diseases associated with abnormal accumulation of…”
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LIK066, a Dual SGLT1/2 Inhibitor, Reduces Weight and Improves Multiple Incretin Hormones in Clinical Proof-of-Concept Studies in Obese Patients With or Without Diabetes
Published in Diabetes (New York, N.Y.) (01-07-2018)“…Background: LIK066 is a potent dual inhibitor of SGLT1/2 (IC50: 20.6 and 0.58 nM for SGLT1 and SGLT2). We studied mechanistic effects of dual SGLT1/2…”
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Abstract 456: Assessment of Pharmacokinetic Drug Interaction between LCZ696 and Metformin
Published in Hypertension (Dallas, Tex. 1979) (01-09-2013)“…Abstract only Objective: LCZ696 is a first-in-class angiotensin receptor neprilysin inhibitor (ARNI) being developed for the treatment of cardiovascular…”
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Pharmacokinetic drug-drug interaction assessment of LCZ696 (an angiotensin receptor neprilysin inhibitor) with omeprazole, metformin or levonorgestrel-ethinyl estradiol in healthy subjects
Published in Clinical pharmacology in drug development (01-01-2016)“…LCZ696 is a novel angiotensin receptor neprilysin inhibitor in development for the treatment of cardiovascular diseases. Here, we assessed the potential for…”
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