Trials that use: Multiplicity adjustment
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20,317 results
- Study to Evaluate Efficacy and Safety of BGB-3111 in Participants With Relapsed or Refractory Mantle Cell Lymphoma (MCL): Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Efficacy and Safety of BGB-3111 in Participants With Relapsed or Refractory Mantle Cell Lymphoma (MCL): primary endpoint results, effect estimate with confidence interval, sample-size planning…
- Study to Evaluate Efficacy, Safety and Immunogenicity of GSK Biologicals’ Herpes Zoster (HZ) Vaccine GSK1437173A in Adults Aged 50 Years and Older: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Efficacy, Safety and Immunogenicity of GSK Biologicals' Herpes Zoster (HZ) Vaccine GSK1437173A in Adults Aged 50 Years and Older: primary endpoint results, effect estimate with…
- Study to Evaluate Efficacy, Safety, and Immunogenicity of GlaxoSmithKline (GSK) Biologicals’ Herpes Zoster Vaccine GSK1437173A: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Efficacy, Safety, and Immunogenicity of GlaxoSmithKline (GSK) Biologicals' Herpes Zoster Vaccine GSK1437173A: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety,…
- Study to Evaluate Efficacy, Safety, Tolerability, and Pharmacodynamics of Entospletinib in Adults With Relapsed or Refractory Hematologic Malignancies: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Efficacy, Safety, Tolerability, and Pharmacodynamics of Entospletinib in Adults With Relapsed or Refractory Hematologic Malignancies: primary endpoint results, effect estimate with confidence interval, sample-size planning…
- Study to Evaluate GSK Biologicals’ Herpes Zoster Vaccine GSK1437173A in Human Immunodeficiency Virus (HIV)-Infected Subjects: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate GSK Biologicals' Herpes Zoster Vaccine GSK1437173A in Human Immunodeficiency Virus (HIV)-Infected Subjects: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety,…
- Study to Evaluate Ibrutinib Combination Therapy in Patients With Selected Gastrointestinal and Genitourinary Tumors: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Ibrutinib Combination Therapy in Patients With Selected Gastrointestinal and Genitourinary Tumors: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based…
- Study to Evaluate Immunogenicity and Safety of GlaxoSmithKline (GSK) Biologicals’ Quadrivalent Influenza Vaccine GSK2282512A When Administered to Children From 6 to 35 Months of Age: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Immunogenicity and Safety of GlaxoSmithKline (GSK) Biologicals' Quadrivalent Influenza Vaccine GSK2282512A When Administered to Children From 6 to 35 Months of Age: primary endpoint results,…
- Study to Evaluate Immunogenicity and Safety of GSK Biologicals’ Herpes Zoster Subunit (HZ/su) Vaccine at 9 and 10 Years After Vaccine Administration and Assessment of Re-vaccination With 2 Additional Doses at 10 Years After Initial Vaccination, in Healthy Subjects Aged 60 Years of Age(YOA) and Older: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Immunogenicity and Safety of GSK Biologicals' Herpes Zoster Subunit (HZ/su) Vaccine at 9 and 10 Years After Vaccine Administration and Assessment of Re-vaccination With 2…
- Study to Evaluate Immunological Equivalence Between Two Investigational Influenza Vaccines in Adults (H1N1): Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Immunological Equivalence Between Two Investigational Influenza Vaccines in Adults (H1N1): primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on…
- Study to Evaluate Intravenous and Oral Steroids for Multiple Sclerosis Attacks: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Intravenous and Oral Steroids for Multiple Sclerosis Attacks: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov results…
- Study to Evaluate MK-6096 in the Treatment of Painful Diabetic Neuropathy (PDN) in Adults (MK-6096-021): Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate MK-6096 in the Treatment of Painful Diabetic Neuropathy (PDN) in Adults (MK-6096-021): primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety,…
- Study to Evaluate Palifermin in the Reduction of Dysphagia in Patients With Locally Advanced Non-Small Cell Lung Cancer (NSCLC): Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Palifermin in the Reduction of Dysphagia in Patients With Locally Advanced Non-Small Cell Lung Cancer (NSCLC): primary endpoint results, effect estimate with confidence interval, sample-size…
- Study to Evaluate PF-04965842 in Patients With Moderate to Severe Psoriasis: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate PF-04965842 in Patients With Moderate to Severe Psoriasis: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov results…
- Study to Evaluate Pharmacokinetic (PK), Safety and Tolerability of Cabotegravir (CAB) 400 Milligrams Per Milliliter (mg/mL) Formulation in Healthy Adult Participants: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Pharmacokinetic (PK), Safety and Tolerability of Cabotegravir (CAB) 400 Milligrams Per Milliliter (mg/mL) Formulation in Healthy Adult Participants: primary endpoint results, effect estimate with confidence…
- Study to Evaluate Pharmacokinetic Comparability Between AZD7442 Co-formulation (AZD8895 + AZD1061) vs AZD8895 and AZD1061 Individually in Adult Healthy Participants: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Pharmacokinetic Comparability Between AZD7442 Co-formulation (AZD8895 + AZD1061) vs AZD8895 and AZD1061 Individually in Adult Healthy Participants: primary endpoint results, effect estimate with confidence interval,…
- Study to Evaluate Potential Decrease in Hospitalization Events, Time Between Events, and Increasing Longevity in Patients With Symptomatic Heart Failure (0954-948): Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Potential Decrease in Hospitalization Events, Time Between Events, and Increasing Longevity in Patients With Symptomatic Heart Failure (0954-948): primary endpoint results, effect estimate with confidence…
- Study to Evaluate Product Duration of Use Experience With Alclometasone Dipropionate Cream: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Product Duration of Use Experience With Alclometasone Dipropionate Cream: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov…
- Study to Evaluate Romosozumab in Children and Adolescents With Osteogenesis Imperfecta: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Romosozumab in Children and Adolescents With Osteogenesis Imperfecta: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov results…
- Study to Evaluate Safety & Efficacy of d-Amphetamine Transdermal System vs Placebo in Children & Adolescents With ADHD: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Safety & Efficacy of d-Amphetamine Transdermal System vs Placebo in Children & Adolescents With ADHD: primary endpoint results, effect estimate with confidence interval, sample-size planning…
- Study to Evaluate Safety & Efficacy of Sarecycline in Treatment of Acne: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Safety & Efficacy of Sarecycline in Treatment of Acne: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov…
- Study to Evaluate Safety and Activity of TRL345 in Healthy Volunteers: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Safety and Activity of TRL345 in Healthy Volunteers: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov results…
- Study to Evaluate Safety and Antiviral Activity of Doses of JNJ-53718678 in Children (>=28 Days to <=3 Years) With Respiratory Syncytial Virus Infection: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Safety and Antiviral Activity of Doses of JNJ-53718678 in Children (>=28 Days to
- Study to Evaluate Safety and Immunogenicity of Sub-unit Adjuvanted Influenza Vaccine Administered to Elderly Subjects, Formulation 2011-2012: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Safety and Immunogenicity of Sub-unit Adjuvanted Influenza Vaccine Administered to Elderly Subjects, Formulation 2011-2012: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration,…
- Study to Evaluate Safety and Tolerability of a Single Dose of PF-06741086 in Chinese Adult Participants With Severe Hemophilia: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Safety and Tolerability of a Single Dose of PF-06741086 in Chinese Adult Participants With Severe Hemophilia: primary endpoint results, effect estimate with confidence interval, sample-size…
- Study to Evaluate Safety of Vitamin D Receptor Activators in Patients Ages 0 to 16 With Chronic Kidney Disease Stage 5 Receiving Peritoneal Dialysis Within Current Clinical Practice: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Safety of Vitamin D Receptor Activators in Patients Ages 0 to 16 With Chronic Kidney Disease Stage 5 Receiving Peritoneal Dialysis Within Current Clinical Practice:…
- Study to Evaluate Safety, Efficacy and Tolerability of Clobetasol Propionate for Chronic Hand Dermatitis: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Safety, Efficacy and Tolerability of Clobetasol Propionate for Chronic Hand Dermatitis: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based…
- Study to Evaluate Safety, Tolerability & Immunogenicity of BNT162b2 in Immunocompromised Participants ≥2 Years: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Safety, Tolerability & Immunogenicity of BNT162b2 in Immunocompromised Participants ≥2 Years: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based…
- Study to Evaluate Safety, Tolerability, and Immunogenicity of Candidate Human Cytomegalovirus Vaccine in Healthy Adults: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Safety, Tolerability, and Immunogenicity of Candidate Human Cytomegalovirus Vaccine in Healthy Adults: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety,…
- Study to Evaluate Safety, Tolerability, Pharmacokinetics & Pharmacodynamics of JTT-662 in Subjects With Type 2 Diabetes: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Safety, Tolerability, Pharmacokinetics & Pharmacodynamics of JTT-662 in Subjects With Type 2 Diabetes: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and…
- Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Antiviral Activity of Voxilaprevir in Adults With Chronic Hepatitis C Virus Infection: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Antiviral Activity of Voxilaprevir in Adults With Chronic Hepatitis C Virus Infection: primary endpoint results, effect estimate with confidence interval, sample-size…
- Study to Evaluate Subject Satisfaction With Facial Appearance and Impact of Combined Facial Treatment: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Subject Satisfaction With Facial Appearance and Impact of Combined Facial Treatment: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based…
- Study to Evaluate Switching From Regimens Consisting of a Ritonavir-boosted Protease Inhibitor (PI) and Two Nucleoside Reverse Transcriptase Inhibitors (NRTIs) to a Fixed-dose Tablet Containing Emtricitabine/Rilpivirine/Tenofovir DF: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Switching From Regimens Consisting of a Ritonavir-boosted Protease Inhibitor (PI) and Two Nucleoside Reverse Transcriptase Inhibitors (NRTIs) to a Fixed-dose Tablet Containing Emtricitabine/Rilpivirine/Tenofovir DF: primary…
- Study to Evaluate Switching to Elvitegravir/Cobicistat/Emtricitabine/Tenofovir Alafenamide (E/C/F/TAF) Fixed Dose Combination (FDC) in Virologically-Suppressed HIV-1 Infected Adults Harboring the Archived Isolated NRTI Resistance Mutation M184V/M184I: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Switching to Elvitegravir/Cobicistat/Emtricitabine/Tenofovir Alafenamide (E/C/F/TAF) Fixed Dose Combination (FDC) in Virologically-Suppressed HIV-1 Infected Adults Harboring the Archived Isolated NRTI Resistance Mutation M184V/M184I: primary endpoint results,…
- Study to Evaluate Symptoms in Patients Treated With Nebivolol or Metoprolol Extended-release (ER) for Hypertension: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Symptoms in Patients Treated With Nebivolol or Metoprolol Extended-release (ER) for Hypertension: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety,…
- Study to Evaluate the 24-Hour Pulmonary Function Profile of Fluticasone Furoate/Vilanterol (FF/VI) Inhalation Powder 100/25mcg Once Daily Compared With Tiotropium Bromide Inhalation Powder 18mcg Once Daily in Subjects With COPD Who Have or Are At Risk for Co-morbid Cardiovascular Disease: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the 24-Hour Pulmonary Function Profile of Fluticasone Furoate/Vilanterol (FF/VI) Inhalation Powder 100/25mcg Once Daily Compared With Tiotropium Bromide Inhalation Powder 18mcg Once Daily in Subjects…
- Study to Evaluate the Analgesic Efficacy of 28 Days’ Oral Administration of AZD2066 Compared With Placebo in Patients With Painful Diabetic Neuropathy: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Analgesic Efficacy of 28 Days' Oral Administration of AZD2066 Compared With Placebo in Patients With Painful Diabetic Neuropathy: primary endpoint results, effect estimate with…
- Study to Evaluate the Antiviral Activity, Clinical Outcomes, Safety, Tolerability, and Pharmacokinetics of Orally Administered Lumicitabine Regimens in Adult Participants Hospitalized With Respiratory Syncytial Virus: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Antiviral Activity, Clinical Outcomes, Safety, Tolerability, and Pharmacokinetics of Orally Administered Lumicitabine Regimens in Adult Participants Hospitalized With Respiratory Syncytial Virus: primary endpoint results,…
- Study to Evaluate the Clinical Activity and Safety of Oral NX-13 in Moderate to Severe Ulcerative Colitis: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Clinical Activity and Safety of Oral NX-13 in Moderate to Severe Ulcerative Colitis: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration,…
- Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Contraceptive Efficacy/Safety of a Low Dose EE/LNG Transdermal Contraceptive Delivery System: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety,…
- Study to Evaluate the Effect of GWP42003 on Liver Fat Levels in Participants With Fatty Liver Disease: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Effect of GWP42003 on Liver Fat Levels in Participants With Fatty Liver Disease: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration,…
- Study to Evaluate the Effect of Nicotinamide Riboside on Immunity: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Effect of Nicotinamide Riboside on Immunity: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov results (NCT02812238).
- Study To Evaluate The Effect Of Two Steady State Doses of PF 06882961 On Rosuvastatin And Midazolam Pharmacokinetics In Otherwise Healthy Adult Participants With Obesity: Complete Statistical AnalysisIndependent statistical analysis of Study To Evaluate The Effect Of Two Steady State Doses of PF 06882961 On Rosuvastatin And Midazolam Pharmacokinetics In Otherwise Healthy Adult Participants With Obesity: primary endpoint results,…
- Study to Evaluate the Effect of XmAb®5871 on Disease Activity in Patients With IgG4-Related Disease (RD): Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Effect of XmAb®5871 on Disease Activity in Patients With IgG4-Related Disease (RD): primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and…
- Study to Evaluate the Effect on Parameters of Systemic Inflammation and Disease Outcomes and Safety of RPH-104 in Subjects With Acute ST-elevation Myocardial Infarction: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Effect on Parameters of Systemic Inflammation and Disease Outcomes and Safety of RPH-104 in Subjects With Acute ST-elevation Myocardial Infarction: primary endpoint results, effect…
- Study to Evaluate the Effectiveness and Safety of MK-1029 in the Treatment of Persistent Asthma That is Not Controlled With Montelukast (ML) in Adults (MK-1029-011): Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Effectiveness and Safety of MK-1029 in the Treatment of Persistent Asthma That is Not Controlled With Montelukast (ML) in Adults (MK-1029-011): primary endpoint results,…
- Study to Evaluate the Effectiveness of DRG Stimulation for Discogenic Low Back Pain: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Effectiveness of DRG Stimulation for Discogenic Low Back Pain: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on…
- Study to Evaluate the Effectiveness of Test Dentifrice in the Relief of Dentinal Hypersensitivity: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Effectiveness of Test Dentifrice in the Relief of Dentinal Hypersensitivity: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based…
- Study to Evaluate the Effects of a High-Fat Meal on Bexagliflozin in Healthy Subjects: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Effects of a High-Fat Meal on Bexagliflozin in Healthy Subjects: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based…
- Study to Evaluate the Effects of MEDI6012 on Apolipoprotein B100 Metabolism: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Effects of MEDI6012 on Apolipoprotein B100 Metabolism: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov results…
- Study to Evaluate the Efficacy and Safety of Aliskiren Alone and in Combination With Amlodipine in Essential Hypertension: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Efficacy and Safety of Aliskiren Alone and in Combination With Amlodipine in Essential Hypertension: primary endpoint results, effect estimate with confidence interval, sample-size planning…