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Pharmacokinetics and safety of bilastine in children aged 6 to 11 years with allergic rhinoconjunctivitis or chronic urticaria

European journal of pediatrics, 2020-05, Vol.179 (5), p.801-805

2020

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Bilastine vs. hydroxyzine: occupation of brain histamine H1‐receptors evaluated by positron emission tomography in healthy volunteers

British journal of clinical pharmacology, 2014-11, Vol.78 (5), p.970-980

2014

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Synthesis, biological evaluation, and docking studies of novel heterocyclic diaryl compounds as selective COX-2 inhibitors

Bioorganic & medicinal chemistry, 2010-09, Vol.18 (17), p.6367-6376

2010

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Bilastine in allergic rhinoconjunctivitis and urticaria: a practical approach to treatment decisions based on queries received by the medical information department

Drugs in Context, 2017, Vol.6, p.212500-13

2017

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The long duration of action of the second generation antihistamine bilastine coincides with its long residence time at the histamine H 1 receptor

European journal of pharmacology, 2018-11, Vol.838, p.107

2018

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The long duration of action of the second generation antihistamine bilastine coincides with its long residence time at the histamine H1 receptor

European journal of pharmacology, 2018-11, Vol.838, p.107-111

2018

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Lack of Clinical Relevance of Bilastine-Food Interaction in Healthy Volunteers: A Wheal and Flare Study

International archives of allergy and immunology, 2022-12, Vol.183 (12), p.1241-1250

2022

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Model-informed pediatric development applied to bilastine: Analysis of the clinical PK data and confirmation of the dose selected for the target population

European journal of pharmaceutical sciences, 2019-02, Vol.128, p.180-192

2019

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Efficacy and safety of bilastine in reducing pruritus in patients with chronic spontaneous urticaria and other skin diseases: an exploratory study

The Journal of dermatological treatment, 2020-04, Vol.31 (3), p.270-278

2020

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Comparative efficacy of bilastine, desloratadine and rupatadine in the suppression of wheal and flare response induced by intradermal histamine in healthy volunteers

Current medical research and opinion, 2017-01, Vol.33 (1), p.129-136

2017

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Bilastine vs. hydroxyzine: occupation of brain histamine H 1 ‐receptors evaluated by positron emission tomography in healthy volunteers

British journal of clinical pharmacology, 2014-11, Vol.78 (5), p.970-980

2014

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Bioequivalence Evaluation of Three Pediatric Oral Formulations of Bilastine in Healthy Subjects: Results from a Randomized, Open Label, Crossover Study

European journal of drug metabolism and pharmacokinetics, 2020-04, Vol.45 (2), p.265-272

2020

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Bilastine: a new antihistamine with an optimal benefit-to-risk ratio for safety during driving

Expert opinion on drug safety, 2016-01, Vol.15 (1), p.89-98

2016

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Cognitive Performance Effects of Bilastine 20 mg During 6 Hours at 8000 ft Cabin Altitude

Aerospace medicine and human performance, 2016-07, Vol.87 (7), p.622-627

2016

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Open-label safety assessment of bilastine in elderly patients with allergic rhinoconjunctivitis and/or urticaria

Allergy and asthma proceedings, 2018-07, Vol.39 (4), p.299-304

2018

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Novel 2-(4-methylsulfonylphenyl)pyrimidine derivatives as highly potent and specific COX-2 inhibitors

Bioorganic & medicinal chemistry, 2008-03, Vol.16 (5), p.2183-2199

2008

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Synthesis and pharmacological characterization of a new benzoxazole derivative as a potent 5-HT 3 receptor agonist

Bioorganic & medicinal chemistry, 2003-07, Vol.11 (13), p.2709-2714

2003

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Reversal of learned helplessness by selective serotonin reuptake inhibitors in rats is not dependent on 5-HT availability

Neuropharmacology, 2007-03, Vol.52 (3), p.975-984

2007

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Synthesis and biological evaluation of 4,5-diphenyloxazolone derivatives on route towards selective COX-2 inhibitors

European journal of medicinal chemistry, 2009-05, Vol.44 (5), p.1830-1837

2009

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In vitro and in vivo characterization of F-97013-GD, a partial 5-HT1A agonist with antipsychotic- and antiparkinsonian-like properties

Neuropharmacology, 2006-07, Vol.51 (1), p.129-140

2006

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In vivo pharmacological characterisation of bilastine, a potent and selective histamine H1 receptor antagonist

Drugs in R&D, 2006, Vol.7 (4), p.219-231

2006

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Syntheses and Binding Studies of New [(Aryl)(aryloxy)methyl]piperidine Derivatives and Related Compounds as Potential Antidepressant Drugs with High Affinity for Serotonin (5-HT) and Norepinephrine (NE) Transporters

Journal of medicinal chemistry, 2003-12, Vol.46 (25), p.5512-5532

2003

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New 2-Piperazinylbenzimidazole Derivatives as 5-HT3 Antagonists. Synthesis and Pharmacological Evaluation

Journal of medicinal chemistry, 1997-02, Vol.40 (4), p.586-593

1997

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Preclinical pharmacology of F-98214-TA, a novel potent serotonin and norepinephrine uptake inhibitor with antidepressant and anxiolytic properties

Psychopharmacologia, 2005-11, Vol.182 (3), p.400-413

2005

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Synthesis and pharmacological characterization of a new benzoxazole derivative as a potent 5-HT3 receptor agonist

Bioorganic & medicinal chemistry, 2003-07, Vol.11 (13), p.2709-2714

2003

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Pharmacokinetics and safety of bilastine in children aged 6 to 11 years with allergic rhinoconjunctivitis or chronic urticaria

Bilastine vs. hydroxyzine: occupation of brain histamine H1‐receptors evaluated by positron emission tomography in healthy volunteers

Synthesis, biological evaluation, and docking studies of novel heterocyclic diaryl compounds as selective COX-2 inhibitors

Bilastine in allergic rhinoconjunctivitis and urticaria: a practical approach to treatment decisions based on queries received by the medical information department

The long duration of action of the second generation antihistamine bilastine coincides with its long residence time at the histamine H 1 receptor

The long duration of action of the second generation antihistamine bilastine coincides with its long residence time at the histamine H1 receptor

Lack of Clinical Relevance of Bilastine-Food Interaction in Healthy Volunteers: A Wheal and Flare Study

Model-informed pediatric development applied to bilastine: Analysis of the clinical PK data and confirmation of the dose selected for the target population

Efficacy and safety of bilastine in reducing pruritus in patients with chronic spontaneous urticaria and other skin diseases: an exploratory study

Comparative efficacy of bilastine, desloratadine and rupatadine in the suppression of wheal and flare response induced by intradermal histamine in healthy volunteers

Bilastine vs. hydroxyzine: occupation of brain histamine H 1 ‐receptors evaluated by positron emission tomography in healthy volunteers

Bioequivalence Evaluation of Three Pediatric Oral Formulations of Bilastine in Healthy Subjects: Results from a Randomized, Open Label, Crossover Study

Bilastine: a new antihistamine with an optimal benefit-to-risk ratio for safety during driving

Cognitive Performance Effects of Bilastine 20 mg During 6 Hours at 8000 ft Cabin Altitude

Open-label safety assessment of bilastine in elderly patients with allergic rhinoconjunctivitis and/or urticaria

Novel 2-(4-methylsulfonylphenyl)pyrimidine derivatives as highly potent and specific COX-2 inhibitors

Synthesis and pharmacological characterization of a new benzoxazole derivative as a potent 5-HT 3 receptor agonist

Reversal of learned helplessness by selective serotonin reuptake inhibitors in rats is not dependent on 5-HT availability

Synthesis and biological evaluation of 4,5-diphenyloxazolone derivatives on route towards selective COX-2 inhibitors

In vitro and in vivo characterization of F-97013-GD, a partial 5-HT1A agonist with antipsychotic- and antiparkinsonian-like properties

In vivo pharmacological characterisation of bilastine, a potent and selective histamine H1 receptor antagonist

Syntheses and Binding Studies of New [(Aryl)(aryloxy)methyl]piperidine Derivatives and Related Compounds as Potential Antidepressant Drugs with High Affinity for Serotonin (5-HT) and Norepinephrine (NE) Transporters

New 2-Piperazinylbenzimidazole Derivatives as 5-HT3 Antagonists. Synthesis and Pharmacological Evaluation

Preclinical pharmacology of F-98214-TA, a novel potent serotonin and norepinephrine uptake inhibitor with antidepressant and anxiolytic properties

Synthesis and pharmacological characterization of a new benzoxazole derivative as a potent 5-HT3 receptor agonist

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