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Pharmacokinetics and pharmacodynamics of single and multiple doses of the glucagon receptor antagonist LGD‐6972 in healthy subjects and subjects with type 2 diabetes mellitus

Diabetes, obesity & metabolism, 2017-01, Vol.19 (1), p.24-32

2017

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Phase IIa cross-over study of propylene glycol-free melphalan (LGD-353) and alkeran in multiple myeloma autologous transplantation

Bone marrow transplantation (Basingstoke), 2014-08, Vol.49 (8), p.1042-1045

2014

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Comment on the formulation of intravenous topiramate for the treatment of status epilepticus

Epilepsy & behavior, 2023-08, Vol.145, p.109314-109314, Article 109314

2023

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The Effects of Substituted Cyclodextrins on the Colloidal and Conformational Stability of Selected Proteins

Journal of pharmaceutical sciences, 2010-06, Vol.99 (6), p.2800-2818

2010

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Huge solubility increase of poorly water-soluble pharmaceuticals by sulfobutylether-β-cyclodextrin complexation in a low-melting mixture

Environmental chemistry letters, 2022-06, Vol.20 (3), p.1561-1568

2022

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Captisol®: an efficient carrier and solubilizing agent for essential oils and their components

Flavour and fragrance journal, 2017-09, Vol.32 (5), p.340-346

2017

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Evaluation of sustained/controlled-release dosage forms of 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors in dogs and humans

Pharmaceutical research, 1993-11, Vol.10 (11), p.1683-1687

1993

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Formation, isolation and identification of oligomers of aztreonam

European journal of pharmaceutical sciences, 1995-10, Vol.3 (5), p.281-291

1995

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A Phase IIa, Open-Label, Randomized, Pharmacokinetic Comparative, Cross-Over Studyof Melphalan HCl for Injection (propylene glycol-free) and Alkeran for Injection for Myeloablative Conditioning In Multiple Myeloma Patients Undergoing Autologous Transplantation

Blood, 2010-11, Vol.116 (21), p.4525-4525

2010

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Dissolution and Ionization of Warfarin

Journal of pharmaceutical sciences, 1984-07, Vol.73 (7), p.946-948

1984

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Enhanced bioavailability of cefoxitin using palmitoylcarnitine. II: Use of directly compressed tablet formulations in the rat and dog

Pharmaceutical research, 1993-10, Vol.10 (10), p.1516-1520

1993

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Tautomerism of phenindione, 2-phenyl-1,3-indandione, in dipolar aprotic/hydrocarbon solvent mixtures

Journal of the American Chemical Society, 1982-12, Vol.104 (24), p.6672-6680

1982

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Thiamine Whole Blood and Urinary Pharmacokinetics in Rats: Urethan-Induced Dose-Dependent Pharmacokinetics

Journal of pharmaceutical sciences, 1982-02, Vol.71 (2), p.169-172

1982

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Quality of Life (QOL) in Ragweed Allergic Patients Treated with Captisol-Enabled ® Budesonide Nasal Solution (32μg/spray) when Exposed to Ragweed Pollen in an Environmental Exposure Chamber (EEC) Using an EEC-Specific Rhinoconjunctivitis Quality of Life Questionnaire (EEC-RQOLQ)

Journal of allergy and clinical immunology, 2008-02, Vol.121 (2), p.S55-S55

2008

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The Combination Product Captisol-Enabled® Budesonide + Azelastine HCl Nasal Spray Provides Significant, Long-lasting Relief of Ocular Allergy Symptoms in Ragweed Allergic Patients Studied in an Environmental Exposure Chamber (EEC)

Journal of allergy and clinical immunology, 2009-02, Vol.123 (2), p.S130-S130

2009

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Phenylbutazone Ionization Kinetics

Journal of pharmaceutical sciences, 1976-08, Vol.65 (8), p.1161-1165

1976

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Application site dependent ocular absorption of timolol

Journal of ocular pharmacology, 1988, Vol.4 (4), p.335-343

1988

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Phenindione solubility in mixed organic solvents: analysis of the role of specific hydrogen and non-hydrogen bonding interactions

International journal of pharmaceutics, 1983-01, Vol.14 (2), p.263-277

1983

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Controlled drug delivery devices for experimental ocular studies with timolol 2. Ocular and systemic absorption in rabbits

International journal of pharmaceutics, 1990-06, Vol.61 (3), p.241-249

1990

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Controlled drug delivery devices for experimental ocular studies with timolol. I, In vitro release studies

International journal of pharmaceutics, 1990, Vol.61 (3), p.235-240

1990

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Controlled drug delivery devices for experimental ocular studies with timolol. II, Ocular and systemic absorption in rabbits

International journal of pharmaceutics, 1990, Vol.61 (3), p.241-249

1990

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Thiamine whole blood pharmackinetics in rats using both a specific S-thiamine liquid scintillation assay and the thiochrome fluorescence assay

Journal of pharmaceutical sciences, 1978-06, Vol.67 (6), p.818-821

1978

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Thiamine Whole Blood Pharmacokinetics in Rats Using Both a Specific 35S-Thiamine Liquid Scintillation Assay and the Thiochrome Fluorescence Assay

Journal of pharmaceutical sciences, 1978-06, Vol.67 (6), p.818-821

1978

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ChemInform Abstract: TAUTOMERISM OF PHENINDIONE, 2‐PHENYL‐1,3‐INDANDIONE, IN DIPOLAR APROTIC/HYDROCARBON SOLVENT MIXTURES

Chemischer Informationsdienst, 1983-03, Vol.14 (9)

1983

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The transcription factor NFAT promotes exhaustion of activated CD8⁺ T cells

Immunity (Cambridge, Mass.), 2015-02, Vol.42 (2), p.265-278

2015

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Pharmacokinetics and pharmacodynamics of single and multiple doses of the glucagon receptor antagonist LGD‐6972 in healthy subjects and subjects with type 2 diabetes mellitus

Phase IIa cross-over study of propylene glycol-free melphalan (LGD-353) and alkeran in multiple myeloma autologous transplantation

Comment on the formulation of intravenous topiramate for the treatment of status epilepticus

The Effects of Substituted Cyclodextrins on the Colloidal and Conformational Stability of Selected Proteins

Huge solubility increase of poorly water-soluble pharmaceuticals by sulfobutylether-β-cyclodextrin complexation in a low-melting mixture

Captisol®: an efficient carrier and solubilizing agent for essential oils and their components

Evaluation of sustained/controlled-release dosage forms of 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors in dogs and humans

Formation, isolation and identification of oligomers of aztreonam

A Phase IIa, Open-Label, Randomized, Pharmacokinetic Comparative, Cross-Over Studyof Melphalan HCl for Injection (propylene glycol-free) and Alkeran for Injection for Myeloablative Conditioning In Multiple Myeloma Patients Undergoing Autologous Transplantation

Dissolution and Ionization of Warfarin

Enhanced bioavailability of cefoxitin using palmitoylcarnitine. II: Use of directly compressed tablet formulations in the rat and dog

Tautomerism of phenindione, 2-phenyl-1,3-indandione, in dipolar aprotic/hydrocarbon solvent mixtures

Thiamine Whole Blood and Urinary Pharmacokinetics in Rats: Urethan-Induced Dose-Dependent Pharmacokinetics

Quality of Life (QOL) in Ragweed Allergic Patients Treated with Captisol-Enabled ® Budesonide Nasal Solution (32μg/spray) when Exposed to Ragweed Pollen in an Environmental Exposure Chamber (EEC) Using an EEC-Specific Rhinoconjunctivitis Quality of Life Questionnaire (EEC-RQOLQ)

The Combination Product Captisol-Enabled® Budesonide + Azelastine HCl Nasal Spray Provides Significant, Long-lasting Relief of Ocular Allergy Symptoms in Ragweed Allergic Patients Studied in an Environmental Exposure Chamber (EEC)

Phenylbutazone Ionization Kinetics

Application site dependent ocular absorption of timolol

Phenindione solubility in mixed organic solvents: analysis of the role of specific hydrogen and non-hydrogen bonding interactions

Controlled drug delivery devices for experimental ocular studies with timolol 2. Ocular and systemic absorption in rabbits

Controlled drug delivery devices for experimental ocular studies with timolol. I, In vitro release studies

Controlled drug delivery devices for experimental ocular studies with timolol. II, Ocular and systemic absorption in rabbits

Thiamine whole blood pharmackinetics in rats using both a specific S-thiamine liquid scintillation assay and the thiochrome fluorescence assay

Thiamine Whole Blood Pharmacokinetics in Rats Using Both a Specific 35S-Thiamine Liquid Scintillation Assay and the Thiochrome Fluorescence Assay

ChemInform Abstract: TAUTOMERISM OF PHENINDIONE, 2‐PHENYL‐1,3‐INDANDIONE, IN DIPOLAR APROTIC/HYDROCARBON SOLVENT MIXTURES

The transcription factor NFAT promotes exhaustion of activated CD8⁺ T cells

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