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Reply letter to "Vaccine effectiveness of recombinant and standard dose influenza vaccines against outpatient illness during 2018-2019 and 2019-2020 calculated using a retrospective test-negative design"

Human vaccines & immunotherapeutics, 2023-08, Vol.19 (2), p.2227034-2227034

2023

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Reply letter to "Immunogenicity and safety of a quadrivalent high-dose inactivated influenza vaccine compared with a standard-dose quadrivalent influenza vaccine in healthy people aged 60 years or older: a randomized Phase III trial"

Human vaccines & immunotherapeutics, 2022-11, Vol.18 (5), p.2085470-2085470

2022

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Selective Endothelin-A Receptor Antagonism Reduces Proteinuria, Blood Pressure, and Arterial Stiffness in Chronic Proteinuric Kidney Disease

Hypertension (Dallas, Tex. 1979), 2011-04, Vol.57 (4), p.772-779

2011

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Equivalent Systemic Exposure to Fluticasone Propionate/Salmeterol Following Single Inhaled Doses from Advair Diskus and Wixela Inhub: Results of Three Pharmacokinetic Bioequivalence Studies

Journal of aerosol medicine and pulmonary drug delivery, 2020-02, Vol.33 (1), p.34-42

2020

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Randomized, Multicenter Study to Assess the Effects of Different Doses of Sildenafil on Mortality in Adults With Pulmonary Arterial Hypertension

Circulation (New York, N.Y.), 2024-06, Vol.149 (25), p.1949-1959

2024

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A Dose-Response Study Examining the Use of Methacholine Challenge to Demonstrate Local Therapeutic Equivalence of the Salmeterol Component of Generic Inhaled Fluticasone Propionate/Salmeterol Combination Products

Journal of aerosol medicine and pulmonary drug delivery, 2019-12, Vol.32 (6), p.352-363

2019

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A Dose–Response Study to Examine the Methodology for Demonstrating the Local Therapeutic Equivalence of the Fluticasone Propionate Component of an Orally Inhaled Combination Therapy of Fluticasone Propionate/Salmeterol Dry Powder

Journal of aerosol medicine and pulmonary drug delivery, 2019-12, Vol.32 (6), p.364-373

2019

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Comment on: “Safety of Marketed Cancer Supportive Care Biosimilars in the U.S.: A Disproportionality Analysis Using the Food and Drug Administration Adverse Event Reporting System (FAERS) Database”

BioDrugs : clinical immunotherapeutics, biopharmaceuticals, and gene therapy, 2021-05, Vol.35 (3), p.373-374

2021

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Comment on: "Safety of Marketed Cancer Supportive Care Biosimilars in the U.S.: A Disproportionality Analysis Using the Food and Drug Administration Adverse Event Reporting System (FAERS) Database"/Reply

BioDrugs : clinical immunotherapeutics, biopharmaceuticals, and gene therapy, 2021-05, Vol.35 (3), p.373-377

2021

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Clinical Bioequivalence of Wixela Inhub and Advair Diskus in Adults With Asthma

Journal of aerosol medicine and pulmonary drug delivery, 2020-04, Vol.33 (2), p.99-107

2020

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Performance of Multiple-Batch Approaches to Pharmacokinetic Bioequivalence Testing for Orally Inhaled Drug Products with Batch-to-Batch Variability

AAPS PharmSciTech, 2021-08, Vol.22 (7), p.225-225, Article 225

2021

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Particle size and gastrointestinal absorption influence tiotropium pharmacokinetics: a pilot bioequivalence study of PUR0200 and Spiriva HandiHaler

British journal of clinical pharmacology, 2019-03, Vol.85 (3), p.580-589

2019

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Safety and Efficacy of Sildenafil Citrate for the Treatment of Female Sexual Arousal Disorder: A Double-Blind, Placebo Controlled Study

The Journal of urology, 2003-12, Vol.170 (6), p.2333-2338

2003

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62 CHRONIC ENDOTHELIN-A RECEPTOR ANTAGONISM MODIFIES NOVEL CARDIOVASCULAR RISK FACTORS IN CKD

Journal of hypertension, 2012-09, Vol.30 Suppl 1 (Supplement 1), p.e19-e19

2012

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The Use of the Sexual Function Questionnaire as a Screening Tool for Women with Sexual Dysfunction

Journal of sexual medicine, 2005-07, Vol.2 (4), p.469-477

2005

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Efficacy of Sildenafil Citrate (Viagra) in Men with Premature Ejaculation

Journal of sexual medicine, 2005-05, Vol.2 (3), p.368-375

2005

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A placebo‐controlled study investigating the efficacy and safety of the phosphodiesterase type 5 inhibitor UK‐369,003 for the treatment of men with lower urinary tract symptoms associated with clinical benign prostatic hyperplasia

BJU international, 2010-09, Vol.106 (5), p.674-680

2010

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Re: Randomized Controlled Trial to Evaluate Transdermal Testosterone in Female Cancer Survivors With Decreased Libido: North Central Cancer Treatment Group Protocol N02C3

JNCI : Journal of the National Cancer Institute, 2008-10, Vol.100 (20), p.1482-1482

2008

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A tool to assess the quality of a meta-analysis

Research synthesis methods, 2013-12, Vol.4 (4), p.351-366

2013

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Influence of Sildenafil on Genital Engorgement in Women with Female Sexual Arousal Disorder

Journal of sexual medicine, 2012-10, Vol.9 (10), p.2693-2697

2012

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Cross-over trials in practice: tales of the unexpected

Significance (Oxford, England), 2008-12, Vol.5 (4), p.183-184

2008

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Crossing over to cross-over trials

Significance (Oxford, England), 2009-06, Vol.6 (2), p.89-90

2009

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A placebo‐controlled exploratory study investigating the efficacy and safety of the phosphodiesterase type 5 inhibitor UK‐369,003 for the treatment of men with storage lower urinary tract symptoms associated with a clinical diagnosis of overactive bladder

BJU international, 2010-09, Vol.106 (5), p.666-673

2010

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Discovery of a Selective Small-Molecule Melanocortin-4 Receptor Agonist with Efficacy in a Pilot Study of Sexual Dysfunction in Humans

Journal of medicinal chemistry, 2010-04, Vol.53 (8), p.3183-3197

2010

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Modeling and simulation of sexual activity daily diary data of patients with female sexual arousal disorder treated with sildenafil citrate (Viagra®)

Pharmaceutical research, 2006-08, Vol.23 (8), p.1756-1764

2006

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Reply letter to "Vaccine effectiveness of recombinant and standard dose influenza vaccines against outpatient illness during 2018-2019 and 2019-2020 calculated using a retrospective test-negative design"

Reply letter to "Immunogenicity and safety of a quadrivalent high-dose inactivated influenza vaccine compared with a standard-dose quadrivalent influenza vaccine in healthy people aged 60 years or older: a randomized Phase III trial"

Selective Endothelin-A Receptor Antagonism Reduces Proteinuria, Blood Pressure, and Arterial Stiffness in Chronic Proteinuric Kidney Disease

Equivalent Systemic Exposure to Fluticasone Propionate/Salmeterol Following Single Inhaled Doses from Advair Diskus and Wixela Inhub: Results of Three Pharmacokinetic Bioequivalence Studies

Randomized, Multicenter Study to Assess the Effects of Different Doses of Sildenafil on Mortality in Adults With Pulmonary Arterial Hypertension

A Dose-Response Study Examining the Use of Methacholine Challenge to Demonstrate Local Therapeutic Equivalence of the Salmeterol Component of Generic Inhaled Fluticasone Propionate/Salmeterol Combination Products

A Dose–Response Study to Examine the Methodology for Demonstrating the Local Therapeutic Equivalence of the Fluticasone Propionate Component of an Orally Inhaled Combination Therapy of Fluticasone Propionate/Salmeterol Dry Powder

Comment on: “Safety of Marketed Cancer Supportive Care Biosimilars in the U.S.: A Disproportionality Analysis Using the Food and Drug Administration Adverse Event Reporting System (FAERS) Database”

Comment on: "Safety of Marketed Cancer Supportive Care Biosimilars in the U.S.: A Disproportionality Analysis Using the Food and Drug Administration Adverse Event Reporting System (FAERS) Database"/Reply

Clinical Bioequivalence of Wixela Inhub and Advair Diskus in Adults With Asthma

Performance of Multiple-Batch Approaches to Pharmacokinetic Bioequivalence Testing for Orally Inhaled Drug Products with Batch-to-Batch Variability

Particle size and gastrointestinal absorption influence tiotropium pharmacokinetics: a pilot bioequivalence study of PUR0200 and Spiriva HandiHaler

Safety and Efficacy of Sildenafil Citrate for the Treatment of Female Sexual Arousal Disorder: A Double-Blind, Placebo Controlled Study

62 CHRONIC ENDOTHELIN-A RECEPTOR ANTAGONISM MODIFIES NOVEL CARDIOVASCULAR RISK FACTORS IN CKD

The Use of the Sexual Function Questionnaire as a Screening Tool for Women with Sexual Dysfunction

Efficacy of Sildenafil Citrate (Viagra) in Men with Premature Ejaculation

A placebo‐controlled study investigating the efficacy and safety of the phosphodiesterase type 5 inhibitor UK‐369,003 for the treatment of men with lower urinary tract symptoms associated with clinical benign prostatic hyperplasia

Re: Randomized Controlled Trial to Evaluate Transdermal Testosterone in Female Cancer Survivors With Decreased Libido: North Central Cancer Treatment Group Protocol N02C3

A tool to assess the quality of a meta-analysis

Influence of Sildenafil on Genital Engorgement in Women with Female Sexual Arousal Disorder

Cross-over trials in practice: tales of the unexpected

Crossing over to cross-over trials

A placebo‐controlled exploratory study investigating the efficacy and safety of the phosphodiesterase type 5 inhibitor UK‐369,003 for the treatment of men with storage lower urinary tract symptoms associated with a clinical diagnosis of overactive bladder

Discovery of a Selective Small-Molecule Melanocortin-4 Receptor Agonist with Efficacy in a Pilot Study of Sexual Dysfunction in Humans

Modeling and simulation of sexual activity daily diary data of patients with female sexual arousal disorder treated with sildenafil citrate (Viagra®)

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