Search Results - "Neelakantham, Srikanth"
-
1
Abuse and dependence potential of sphingosine-1-phosphate (S1P) receptor modulators used in the treatment of multiple sclerosis: a review of literature and public data
Published in Psychopharmacology (01-01-2022)“…Abuse and misuse of prescription drugs remains an ongoing concern in the USA and worldwide; thus, all centrally active new drugs must be assessed for abuse and…”
Get full text
Journal Article -
2
Siponimod pharmacokinetics, safety, and tolerability in combination with the potent CYP3A4 inhibitor itraconazole in healthy subjects with different CYP2C9 genotypes
Published in European journal of clinical pharmacology (01-11-2019)“…Purpose To evaluate the PK and safety of siponimod, a substrate of CYP2C9/3A4, in the presence or absence of a CYP3A4 inhibitor, itraconazole. Methods This was…”
Get full text
Journal Article -
3
Safety, Tolerability, Pharmacodynamics and Pharmacokinetics of Intravenous Siponimod: A Randomized, Open-label Study in Healthy Subjects
Published in Clinical therapeutics (01-01-2020)“…The goal of this study was to assess the safety, tolerability, pharmacodynamics (PD) and pharmacokinetics (PK) of intravenous (IV) siponimod in healthy…”
Get full text
Journal Article -
4
Bimagrumab improves body composition and insulin sensitivity in insulin‐resistant individuals
Published in Diabetes, obesity & metabolism (01-01-2018)“…Aim To test the hypothesis that an improving body composition in insulin‐resistant individuals could enhance insulin sensitivity. Methods A total of 16 people…”
Get full text
Journal Article -
5
Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of the Novel Non–Bile Acid FXR Agonist Tropifexor (LJN452) in Healthy Volunteers
Published in Clinical pharmacology in drug development (01-04-2020)“…Tropifexor (LJN452) is a potent, orally available, non–bile acid farnesoid X receptor agonist under clinical development for chronic liver diseases. Here, we…”
Get full text
Journal Article -
6
Safety, Tolerability and Pharmacodynamics of Intravenous Siponimod in Healthy Subjects (P3.399)
Published in Neurology (10-04-2018)“…Abstract only…”
Get full text
Journal Article -
7
Absolute Bioavailability of Single, Oral Dose of Siponimod in Healthy Subjects (P3.402)
Published in Neurology (10-04-2018)“…Abstract only…”
Get full text
Journal Article -
8
Siponimod pharmacokinetics, safety, and tolerability in combination with rifampin, a CYP2C9/3A4 inducer, in healthy subjects
Published in European journal of clinical pharmacology (01-12-2018)“…Purpose To assess the potential pharmacokinetic (PK) interactions between siponimod and rifampin, a strong CYP3A4/moderate CYP2C9 inducer, in healthy subjects…”
Get full text
Journal Article -
9
Pharmacokinetics, safety, and tolerability of siponimod (BAF312) in subjects with severe renal impairment: A single-dose, open-label, parallel-group study
Published in International journal of clinical pharmacology and therapeutics (01-01-2017)“…To investigate the pharmacokinetics (PK), safety, and tolerability of siponimod and selected inactive metabolites (M3 and M5) in subjects with varying degrees…”
Get full text
Journal Article -
10
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…”
Get full text
Journal Article -
11
Pharmacokinetic and pharmacodynamic drug-drug interaction assessment between pradigastat and digoxin or warfarin
Published in Journal of clinical pharmacology (01-07-2014)“…Pradigastat, a novel diacylglycerol acyltransferase‐1 inhibitor, was evaluated for both pharmacokinetic (PK) and pharmacodynamic (PD) drug–drug interactions…”
Get full text
Journal Article -
12
Pharmacokinetics, Safety, and Tolerability of Fevipiprant (QAW039), a Novel CRTh2 Receptor Antagonist: Results From 2 Randomized, Phase 1, Placebo-Controlled Studies in Healthy Volunteers
Published in Clinical pharmacology in drug development (01-07-2016)“…We evaluated the pharmacokinetics (PK), safety, and tolerability of a novel oral CRTh2 antagonist, fevipiprant (QAW039), in healthy subjects. Peak…”
Get full text
Journal Article -
13
Effect of pradigastat, a diacylglycerol acyltransferase 1 inhibitor, on the pharmacokinetics of a combination oral contraceptive in healthy female subjects
Published in International journal of clinical pharmacology and therapeutics (01-04-2015)“…We evaluated the potential pharmacokinetic interaction between pradigastat, a potent and selective diacylglycerol acyltransferase 1 inhibitor, and Levora-28®,…”
Get full text
Journal Article -
14
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…”
Get full text
Journal Article -
15
Effect of mavoglurant (AFQ056), a selective mGluR5 antagonist, on the pharmacokinetics of a combined oral contraceptive containing ethinyl estradiol and levonorgestrel in healthy women
Published in International journal of clinical pharmacology and therapeutics (01-07-2015)“…To compare the pharmacokinetics (PKs) of a combination oral contraceptive (OC) when given alone or concomitantly with the selective metabotropic glutamate…”
Get full text
Journal Article -
16
Effect of Pradigastat, a Diacylglycerol Acyltransferase 1 Inhibitor, on the QTcF Interval in Humans
Published in Clinical pharmacology in drug development (01-11-2016)“…Pradigastat, a novel diacylglycerol acyltransferase 1 inhibitor, has been studied in familial chylomicronemia syndrome. To evaluate the effects of…”
Get full text
Journal Article -
17
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…”
Get full text
Journal Article