Search Results - "JANSAT, Josep M"
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Pharmacokinetics, Safety, and Tolerability of a Single 5‐Day Treatment of Tirbanibulin Ointment 1% in 100 cm2: A Phase 1 Maximal‐Use Trial in Patients with Actinic Keratosis
Published in Clinical pharmacology in drug development (01-02-2024)“…Tirbanibulin ointment 1% is approved in the United States and Europe for the treatment of actinic keratosis with demonstrated efficacy, safety, and…”
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2
Pharmacokinetics and safety of aclidinium bromide, a muscarinic antagonist, in adults with normal or impaired renal function: A phase I, open-label, single-dose clinical trial
Published in Clinical therapeutics (01-09-2010)“…Abstract Background: Aclidinium bromide is an inhaled, long-acting muscarinic antagonist currently in development for the treatment of chronic obstructive…”
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3
Identification of the Human Liver Enzymes Involved in the Metabolism of the Antimigraine Agent Almotriptan
Published in Drug metabolism and disposition (01-04-2003)“…Almotriptan is a novel highly selective 5-hydroxytryptamine 1B/1D agonist developed for the acute oral treatment of migraine. The in vitro metabolism of…”
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4
Pharmacokinetics, Safety, and Tolerability of a Single 5-Day Treatment of Tirbanibulin Ointment 1% in 100 cm 2 : A Phase 1 Maximal-Use Trial in Patients with Actinic Keratosis
Published in Clinical pharmacology in drug development (01-02-2024)“…Tirbanibulin ointment 1% is approved in the United States and Europe for the treatment of actinic keratosis with demonstrated efficacy, safety, and…”
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5
Safety and Pharmacokinetics of Multiple Doses of Aclidinium Bromide, a Novel Long-Acting Muscarinic Antagonist for the Treatment of Chronic Obstructive Pulmonary Disease, in Healthy Participants
Published in Journal of clinical pharmacology (01-10-2009)“…Systemic exposure to anticholinergics used for chronic obstructive pulmonary disease (COPD) may lead to side effects. This study assessed safety, tolerability,…”
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6
Safety and Tolerability of Aclidinium Administered Intravenously and Absolute Bioavailability of Inhaled Aclidinium in Healthy Male Participants
Published in Journal of clinical pharmacology (01-06-2012)“…Aclidinium bromide is a long-acting muscarinic antagonist in development for chronic obstructive pulmonary disease treatment. This 2-part, phase I study…”
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7
Incurred sample reproducibility: views and recommendations by the European Bioanalysis Forum
Published in Bioanalysis (01-09-2009)“…Following intensive discussions, review, alignment of procedures and multiple surveys among their member companies, the European Bioanalysis Forum (EBF) is…”
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8
Mass balance and metabolism of aclidinium bromide following intravenous administration of [14C]-aclidinium bromide in healthy subjects
Published in Biopharmaceutics & drug disposition (01-01-2012)“…ABSTRACT Aclidinium bromide is a novel, inhaled long‐acting muscarinic antagonist with low systemic activity developed for the treatment of COPD. It is an…”
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Effect of MAO‐A inhibition on the pharmacokinetics of almotriptan, an antimigraine agent in humans
Published in British journal of clinical pharmacology (01-05-2001)“…Aims To assess the effect of a reversible MAO‐A inhibitor, moclobemide, on the single‐dose pharmacokinetics of almotriptan and assess the clinical…”
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Absolute Bioavailability, Pharmacokinetics, and Urinary Excretion of the Novel Antimigraine Agent Almotriptan in Healthy Male Volunteers
Published in Journal of clinical pharmacology (01-12-2002)“…Absolute bioavailability, pharmacokinetics, and urinary excretion of almotriptan, a novel 5‐HT1B/1D receptor agonist, were studied in 18 healthy males…”
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Pharmacokinetic and pharmacodynamic studies of the histamine H1-receptor antagonist ebastine in dogs
Published in Journal of pharmacy and pharmacology (01-07-1994)“…The pharmacokinetics and pharmacodynamics of ebastine at single oral doses of 10 and 20 mg were studied in six healthy beagle dogs. Plasma concentrations of…”
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Almotriptan, a New Anti‐Migraine Agent: A Review
Published in CNS drug reviews (01-09-2002)“…ABSTRACT Almotriptan is a new anti‐migraine agent with nanomolar affinity for human 5‐HT1B, 5‐HT1D, and 5‐HT1F receptors, weak affinity for 5‐HT1A and 5‐HT7…”
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