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Twenty-eight day safety, antiviral activity, and pharmacokinetics of tenofovir alafenamide for treatment of chronic hepatitis B infection

Journal of hepatology, 2015-03, Vol.62 (3), p.533-540

2015

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The bioequivalence of fixed‐dose combination tablets of bisoprolol and ramipril and its drug‐drug interaction potential

Clinical and translational science, 2022-01, Vol.15 (1), p.158-171

2022

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Next‐day residual effects of flibanserin on simulated driving performance in premenopausal women

Human psychopharmacology, 2017-07, Vol.32 (4), p.e2603-n/a

2017

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Safety and Pharmacokinetics of Chimeric Anti-Shiga Toxin 1 and Anti-Shiga Toxin 2 Monoclonal Antibodies in Healthy Volunteers

Antimicrobial Agents and Chemotherapy, 2009-07, Vol.53 (7), p.3081-3087

2009

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Effect of opicapone multiple‐dose regimens on levodopa pharmacokinetics

British journal of clinical pharmacology, 2017-03, Vol.83 (3), p.540-553

2017

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Effects of renal impairment on the pharmacokinetics of orally administered deferiprone

British journal of clinical pharmacology, 2016-10, Vol.82 (4), p.994-1001

2016

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The oral toll-like receptor-7 agonist GS-9620 in patients with chronic hepatitis B virus infection

Journal of hepatology, 2015-08, Vol.63 (2), p.320-328

2015

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The Oral β-Lactamase SYN-004 (Ribaxamase) Degrades Ceftriaxone Excreted into the Intestine in Phase 2a Clinical Studies

Antimicrobial agents and chemotherapy, 2017-03, Vol.61 (3)

2017

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The safety and acceptability of twice‐daily deferiprone for transfusional iron overload: A multicentre, open‐label, phase 2 study

British journal of haematology, 2022-04, Vol.197 (1), p.e12-e15

2022

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Single‐dose pharmacokinetics of co‐crystal of tramadol–celecoxib: Results of a four‐way randomized open‐label phase I clinical trial in healthy subjects

British journal of clinical pharmacology, 2017-12, Vol.83 (12), p.2718-2728

2017

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Effect of Alcohol Administered With Flibanserin on Dizziness, Syncope, and Hypotension in Healthy, Premenopausal Women

Journal of sexual medicine, 2017-05, Vol.14 (5), p.e331-e331

2017

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Pharmacokinetics of multiple doses of co‐crystal of tramadol–celecoxib: findings from a four‐way randomized open‐label phase I clinical trial

British journal of clinical pharmacology, 2018-01, Vol.84 (1), p.64-78

2018

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Effects of common cold and concomitant administration of nasal decongestant on the pharmacokinetics and pharmacodynamics of nasal glucagon in otherwise healthy participants: A randomized clinical trial

Diabetes, obesity & metabolism, 2018-03, Vol.20 (3), p.646-653

2018

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Pharmacokinetic bioequivalence, safety and acceptability of Ornibel®, a new polymer composition contraceptive vaginal ring (etonogestrel/ethinylestradiol 11.00/3.474 mg) compared with Nuvaring® (etonogestrel/ethinylestradiol 11.7/2.7 mg)

The European journal of contraception & reproductive health care, 2017-11, Vol.22 (6), p.429-438

2017

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A Phase I Assessment of the Safety and Tolerability Profile of Novel Treatments for Acute Allergic Reactions Administered by Intravenous and Intramuscular Injection Formulations

Journal of allergy and clinical immunology, 2013-02, Vol.131 (2), p.AB26-AB26

2013

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The Effect of Food on Tramadol and Celecoxib Bioavailability Following Oral Administration of Co-Crystal of Tramadol–Celecoxib (CTC): A Randomised, Open-Label, Single-Dose, Crossover Study in Healthy Volunteers

Clinical drug investigation, 2018-09, Vol.38 (9), p.819-827

2018

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Single-Dose, Randomized, Open-Label, Two-Way, Crossover Bioequivalence Study of Two Formulations of Pregabalin 300 mg Hard Capsules in Healthy Volunteers Under Fasting Conditions

Drugs in R&D, 2015-06, Vol.15 (2), p.195-201

2015

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Food Effects on the Pharmacokinetics of Doxylamine Hydrogen Succinate 25 mg Film-Coated Tablets: A Single-Dose, Randomized, Two-Period Crossover Study in Healthy Volunteers

Drugs in R&D, 2012-12, Vol.12 (4), p.217-225

2012

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Pharmacokinetic interaction study between eslicarbazepine acetate and topiramate in healthy subjects

Current medical research and opinion, 2010-06, Vol.26 (6), p.1355-1362

2010

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The Oral β-Lactamase SYN-004, Designed to Protect the Gut Microbiome from Biliary Excreted IV Antibiotics, Efficiently Degrades Intestinal Ceftriaxone in Two Phase 2a Clinical Trials

Open forum infectious diseases, 2016-12, Vol.3 (suppl_1)

2016

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Pharmacokinetic Dose Proportionality Between Two Strengths (12.5 mg and 25 mg) of Doxylamine Hydrogen Succinate Film-Coated Tablets in Fasting State: A Single-Dose, Randomized, Two-Period Crossover Study in Healthy Volunteers

Drugs in R&D, 2013-06, Vol.13 (2), p.129-135

2013

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Study on the bioequivalence of two formulations of eplerenone in healthy volunteers under fasting conditions: data from a single-center, randomized, single-dose, open-label, 2-way crossover bioequivalence study

Arzneimittel-Forschung, 2011-01, Vol.61 (3), p.153

2011

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Modulations of collicular visual responses by acoustic stimuli in rabbits

Neuroscience research, 1987-06, Vol.4 (5), p.385-395

1987

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Modulations of collicular visual responses by acoustic stimuli in rabbits

Neuroscience research. Supplement, 1987-06, Vol.4 (5), p.385-395

1987

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Twenty-eight day safety, antiviral activity, and pharmacokinetics of tenofovir alafenamide for treatment of chronic hepatitis B infection

The bioequivalence of fixed‐dose combination tablets of bisoprolol and ramipril and its drug‐drug interaction potential

Next‐day residual effects of flibanserin on simulated driving performance in premenopausal women

Safety and Pharmacokinetics of Chimeric Anti-Shiga Toxin 1 and Anti-Shiga Toxin 2 Monoclonal Antibodies in Healthy Volunteers

Effect of opicapone multiple‐dose regimens on levodopa pharmacokinetics

Effects of renal impairment on the pharmacokinetics of orally administered deferiprone

The oral toll-like receptor-7 agonist GS-9620 in patients with chronic hepatitis B virus infection

The Oral β-Lactamase SYN-004 (Ribaxamase) Degrades Ceftriaxone Excreted into the Intestine in Phase 2a Clinical Studies

Licogliflozin for nonalcoholic steatohepatitis: a randomized, double-blind, placebo-controlled, phase 2a study

The safety and acceptability of twice‐daily deferiprone for transfusional iron overload: A multicentre, open‐label, phase 2 study

Single‐dose pharmacokinetics of co‐crystal of tramadol–celecoxib: Results of a four‐way randomized open‐label phase I clinical trial in healthy subjects

Effect of Alcohol Administered With Flibanserin on Dizziness, Syncope, and Hypotension in Healthy, Premenopausal Women

Pharmacokinetics of multiple doses of co‐crystal of tramadol–celecoxib: findings from a four‐way randomized open‐label phase I clinical trial

Effects of common cold and concomitant administration of nasal decongestant on the pharmacokinetics and pharmacodynamics of nasal glucagon in otherwise healthy participants: A randomized clinical trial

Pharmacokinetic bioequivalence, safety and acceptability of Ornibel®, a new polymer composition contraceptive vaginal ring (etonogestrel/ethinylestradiol 11.00/3.474 mg) compared with Nuvaring® (etonogestrel/ethinylestradiol 11.7/2.7 mg)

A Phase I Assessment of the Safety and Tolerability Profile of Novel Treatments for Acute Allergic Reactions Administered by Intravenous and Intramuscular Injection Formulations

The Effect of Food on Tramadol and Celecoxib Bioavailability Following Oral Administration of Co-Crystal of Tramadol–Celecoxib (CTC): A Randomised, Open-Label, Single-Dose, Crossover Study in Healthy Volunteers

Single-Dose, Randomized, Open-Label, Two-Way, Crossover Bioequivalence Study of Two Formulations of Pregabalin 300 mg Hard Capsules in Healthy Volunteers Under Fasting Conditions

Food Effects on the Pharmacokinetics of Doxylamine Hydrogen Succinate 25 mg Film-Coated Tablets: A Single-Dose, Randomized, Two-Period Crossover Study in Healthy Volunteers

Pharmacokinetic interaction study between eslicarbazepine acetate and topiramate in healthy subjects

The Oral β-Lactamase SYN-004, Designed to Protect the Gut Microbiome from Biliary Excreted IV Antibiotics, Efficiently Degrades Intestinal Ceftriaxone in Two Phase 2a Clinical Trials

Pharmacokinetic Dose Proportionality Between Two Strengths (12.5 mg and 25 mg) of Doxylamine Hydrogen Succinate Film-Coated Tablets in Fasting State: A Single-Dose, Randomized, Two-Period Crossover Study in Healthy Volunteers

Study on the bioequivalence of two formulations of eplerenone in healthy volunteers under fasting conditions: data from a single-center, randomized, single-dose, open-label, 2-way crossover bioequivalence study

Modulations of collicular visual responses by acoustic stimuli in rabbits

Modulations of collicular visual responses by acoustic stimuli in rabbits

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