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Immunogenicity and Safety of an Inactivated Quadrivalent Influenza Vaccine Candidate: A Phase III Randomized Controlled Trial in Children

The Journal of infectious diseases, 2013-08, Vol.208 (4), p.544-553

2013

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Immunogenicity and safety of quadrivalent versus trivalent inactivated influenza vaccine: a randomized, controlled trial in adults

BMC infectious diseases, 2013-05, Vol.13 (1), p.224-224, Article 224

2013

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Effect on Cellular and Humoral Immune Responses of the AS03 Adjuvant System in an A/H1N1/2009 Influenza Virus Vaccine Administered to Adults during Two Randomized Controlled Trials

Clinical and Vaccine Immunology, 2011-05, Vol.18 (5), p.835-843

2011

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Long-Term Persistence of Cell-Mediated and Humoral Responses to A(H1N1)pdm09 Influenza Virus Vaccines and the Role of the AS03 Adjuvant System in Adults during Two Randomized Controlled Trials

Clinical and vaccine immunology, 2017-06, Vol.24 (6)

2017

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Hamster neogenin, a host-cell protein contained in a respiratory syncytial virus candidate vaccine, induces antibody responses in rabbits but not in clinical trial participants

Human vaccines & immunotherapeutics, 2020-06, Vol.16 (6), p.1327-1337

2020

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Evaluation of potential immunogenicity differences between Pandemrix™ and Arepanrix

Human vaccines & immunotherapeutics, 2016-09, Vol.12 (9), p.2289-2298

2016

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Immunogenicity, reactogenicity, and safety of inactivated quadrivalent influenza vaccine candidate versus inactivated trivalent influenza vaccine in healthy adults aged ≥18 years: A phase III, randomized trial

Vaccine, 2014-03, Vol.32 (13), p.1480-1487

2014

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Hemagglutination Inhibition Antibody Titers as a Correlate of Protection Against Seasonal A/H3N2 Influenza Disease

Open forum infectious diseases, 2015-04, Vol.2 (2), p.ofv067-ofv067

2015

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A multi-criteria decision making approach to identify a vaccine formulation

Journal of biopharmaceutical statistics, 2016-03, Vol.26 (2), p.352-364

2016

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Using tolerance intervals in pre-study validation of analytical methods to predict in-study results. The fit-for-future-purpose concept

Journal of chromatography. A, 2007-07, Vol.1158 (1-2), p.126-137

2007

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Risk management for analytical methods based on the total error concept: Conciliating the objectives of the pre-study and in-study validation phases

Chemometrics and intelligent laboratory systems, 2007-04, Vol.86 (2), p.198-207

2007

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Pre-study analytical method validation: comparison of four alternative approaches based on quality-level estimation and tolerance intervals

Quality and reliability engineering international, 2008-10, Vol.24 (6), p.667-680

2008

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Tumor Necrosis Factor α Decreases, and Interleukin-10 Increases, the Sensitivity of Human Monocytes to Dexamethasone: Potential Regulation of the Glucocorticoid Receptor

The journal of clinical endocrinology and metabolism, 1999-08, Vol.84 (8), p.2834-2839

1999

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A Randomized, Controlled, Observer-Blinded Phase 1 Study of the Safety and Immunogenicity of a Respiratory Syncytial Virus Vaccine With or Without Alum Adjuvant

The Journal of infectious diseases, 2017-01, Vol.215 (1), p.24-33

2017

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Long‐term Results of Polyglactin Mesh for the Prevention of Incisional Hernias in Obese Patients

World journal of surgery, 1998-05, Vol.22 (5), p.479-483

1998

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Influenza vaccine efficacy trials: a simulation approach to understand failures from the past

Pharmaceutical statistics : the journal of the pharmaceutical industry, 2015-07, Vol.14 (4), p.294-301

2015

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Exploring drug solubility in fasted human intestinal fluid aspirates: Impact of inter-individual variability, sampling site and dilution

International journal of pharmaceutics, 2017-08, Vol.528 (1-2), p.471-484

2017

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Influence of the nature of the electrolyte on the chiral separation of basic compounds in nonaqueous capillary electrophoresis using heptakis(2,3-di- O-methyl-6- O-sulfo)-β-cyclodextrin

Journal of Chromatography A, 2005-03, Vol.1068 (1), p.143-150

2005

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Harmonization of strategies for the validation of quantitative analytical procedures A SFSTP proposal. Part II

Journal of pharmaceutical and biomedical analysis, 2007-09, Vol.45 (1), p.70-81

2007

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A Phase III Evaluation of Immunogenicity and Safety of Two Trivalent Inactivated Seasonal Influenza Vaccines in US Children

The Pediatric infectious disease journal, 2010-10, Vol.29 (10), p.924-930

2010

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Harmonization of strategies for the validation of quantitative analytical procedures A SFSTP proposal. Part III

Journal of pharmaceutical and biomedical analysis, 2007-09, Vol.45 (1), p.82-96

2007

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Evaluation of a Diphenylphosphorylazide‐Crosslinked Collagen Membrane for Guided Bone Regeneration in Mandibular Defects in Rats

Journal of periodontology (1970), 1998-11, Vol.69 (11), p.1238-1246

1998

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What happens with adverse events during 6 months of treatment with selective serotonin reuptake inhibitors?

The journal of clinical psychiatry, 2005-07, Vol.66 (7), p.859

2005

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Harmonization of strategies for the validation of quantitative analytical procedures: A SFSTP proposal-part I

Journal of pharmaceutical and biomedical analysis, 2004-11, Vol.36 (3), p.579-586

2004

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LC method for the simultaneous determination of R-timolol and other closely related impurities in S-timolol maleate: Optimization by use of an experimental design

Journal of separation science, 2003-07, Vol.26 (9-10), p.809-817

2003

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Immunogenicity and Safety of an Inactivated Quadrivalent Influenza Vaccine Candidate: A Phase III Randomized Controlled Trial in Children

Immunogenicity and safety of quadrivalent versus trivalent inactivated influenza vaccine: a randomized, controlled trial in adults

Effect on Cellular and Humoral Immune Responses of the AS03 Adjuvant System in an A/H1N1/2009 Influenza Virus Vaccine Administered to Adults during Two Randomized Controlled Trials

Long-Term Persistence of Cell-Mediated and Humoral Responses to A(H1N1)pdm09 Influenza Virus Vaccines and the Role of the AS03 Adjuvant System in Adults during Two Randomized Controlled Trials

Hamster neogenin, a host-cell protein contained in a respiratory syncytial virus candidate vaccine, induces antibody responses in rabbits but not in clinical trial participants

Evaluation of potential immunogenicity differences between Pandemrix™ and Arepanrix

Immunogenicity, reactogenicity, and safety of inactivated quadrivalent influenza vaccine candidate versus inactivated trivalent influenza vaccine in healthy adults aged ≥18 years: A phase III, randomized trial

Hemagglutination Inhibition Antibody Titers as a Correlate of Protection Against Seasonal A/H3N2 Influenza Disease

A multi-criteria decision making approach to identify a vaccine formulation

Using tolerance intervals in pre-study validation of analytical methods to predict in-study results. The fit-for-future-purpose concept

Risk management for analytical methods based on the total error concept: Conciliating the objectives of the pre-study and in-study validation phases

Pre-study analytical method validation: comparison of four alternative approaches based on quality-level estimation and tolerance intervals

Tumor Necrosis Factor α Decreases, and Interleukin-10 Increases, the Sensitivity of Human Monocytes to Dexamethasone: Potential Regulation of the Glucocorticoid Receptor

A Randomized, Controlled, Observer-Blinded Phase 1 Study of the Safety and Immunogenicity of a Respiratory Syncytial Virus Vaccine With or Without Alum Adjuvant

Long‐term Results of Polyglactin Mesh for the Prevention of Incisional Hernias in Obese Patients

Influenza vaccine efficacy trials: a simulation approach to understand failures from the past

Exploring drug solubility in fasted human intestinal fluid aspirates: Impact of inter-individual variability, sampling site and dilution

Influence of the nature of the electrolyte on the chiral separation of basic compounds in nonaqueous capillary electrophoresis using heptakis(2,3-di- O-methyl-6- O-sulfo)-β-cyclodextrin

Harmonization of strategies for the validation of quantitative analytical procedures A SFSTP proposal. Part II

A Phase III Evaluation of Immunogenicity and Safety of Two Trivalent Inactivated Seasonal Influenza Vaccines in US Children

Harmonization of strategies for the validation of quantitative analytical procedures A SFSTP proposal. Part III

Evaluation of a Diphenylphosphorylazide‐Crosslinked Collagen Membrane for Guided Bone Regeneration in Mandibular Defects in Rats

What happens with adverse events during 6 months of treatment with selective serotonin reuptake inhibitors?

Harmonization of strategies for the validation of quantitative analytical procedures: A SFSTP proposal-part I

LC method for the simultaneous determination of R-timolol and other closely related impurities in S-timolol maleate: Optimization by use of an experimental design

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