Trials that use: Odds ratio
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5,976 results
- Study to Evaluate the Efficacy and Safety of CC-90001 in Participants With Non-alcoholic Steatohepatitis (NASH) and Liver Fibrosis: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Efficacy and Safety of CC-90001 in Participants With Non-alcoholic Steatohepatitis (NASH) and Liver Fibrosis: primary endpoint results, effect estimate with confidence interval, sample-size planning…
- Study to Evaluate the Efficacy and Safety of PT20 in Subjects With Hyperphosphataemia and Dialysis Dependent Chronic Kidney Disease: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Efficacy and Safety of PT20 in Subjects With Hyperphosphataemia and Dialysis Dependent Chronic Kidney Disease: primary endpoint results, effect estimate with confidence interval, sample-size…
- Study to Evaluate the Efficacy and Safety of Suptavumab (REGN2222) for the Prevention of Medically Attended RSV (Respiratory Syncytial Virus) Infection in Preterm Infants: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Efficacy and Safety of Suptavumab (REGN2222) for the Prevention of Medically Attended RSV (Respiratory Syncytial Virus) Infection in Preterm Infants: primary endpoint results, effect…
- Study to Evaluate the Efficacy and Safety of Tamsulosin in Children With Neurogenic Bladder: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Efficacy and Safety of Tamsulosin in Children With Neurogenic Bladder: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based…
- Study to Evaluate the Efficacy and Safety of Treatment With Bendamustine in Combination With Ofatumumab in Previously Untreated Patients With Indolent B-Cell Non-Hodgkin’s Lymphoma (NHL): Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Efficacy and Safety of Treatment With Bendamustine in Combination With Ofatumumab in Previously Untreated Patients With Indolent B-Cell Non-Hodgkin's Lymphoma (NHL): primary endpoint results,…
- Study to Evaluate the Efficacy and Safety of Vibegron Administered Orally for 12 Weeks to Women With Irritable Bowel Syndrome: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Efficacy and Safety of Vibegron Administered Orally for 12 Weeks to Women With Irritable Bowel Syndrome: primary endpoint results, effect estimate with confidence interval,…
- Study to Evaluate the Efficacy of Etanercept Treatment in Adults Who Failed Therapy With Apremilast: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Efficacy of Etanercept Treatment in Adults Who Failed Therapy With Apremilast: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety,…
- Study to Evaluate the Efficacy, Safety and Immunogenicity of Influenza Vaccine in Healthy Subjects (Aged 6 to <72 Months) Versus Control Vaccines: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Efficacy, Safety and Immunogenicity of Influenza Vaccine in Healthy Subjects (Aged 6 to
- Study to Evaluate the Efficacy, Safety and Tolerability of Bupropion Hydrochloride Extended-release Tablet, and Escitalopram Oxalate Capsule in Subjects With Major Depressive Disorder: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Efficacy, Safety and Tolerability of Bupropion Hydrochloride Extended-release Tablet, and Escitalopram Oxalate Capsule in Subjects With Major Depressive Disorder: primary endpoint results, effect estimate…
- Study to Evaluate the Efficacy, Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Sapablursen (Formerly ISIS 702843, IONIS-TMPRSS6-LRx): Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Efficacy, Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Sapablursen (Formerly ISIS 702843, IONIS-TMPRSS6-LRx): primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and…
- Study to Evaluate the Immune Response After a Booster Dose of a Quadrivalent Meningococcal (MenACYW) Conjugate Vaccine When Administered Alone or Concomitantly With a Licensed Meningococcal Serogroup B Vaccine, in Participants Who Received Primary Quadrivalent Meningococcal Conjugate Vaccine (MCV4): Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Immune Response After a Booster Dose of a Quadrivalent Meningococcal (MenACYW) Conjugate Vaccine When Administered Alone or Concomitantly With a Licensed Meningococcal Serogroup B…
- Study to Evaluate the Immunogenicity and Safety of GlaxoSmithKline (GSK) Biologicals’ Herpes Zoster Vaccine GSK1437173A When Co-administered With GSK Biologicals’ Seasonal Influenza Vaccine GSK2321138A in Adults Aged 50 Years and Older: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Immunogenicity and Safety of GlaxoSmithKline (GSK) Biologicals' Herpes Zoster Vaccine GSK1437173A When Co-administered With GSK Biologicals' Seasonal Influenza Vaccine GSK2321138A in Adults Aged 50…
- Study to Evaluate the Pharmacokinetics and Pharmacodynamics of Dabigatran Etexilate in Patients With Stable Severe Renal Disease.: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Pharmacokinetics and Pharmacodynamics of Dabigatran Etexilate in Patients With Stable Severe Renal Disease.: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration,…
- Study to Evaluate the Safety and Antiviral Activity of Remdesivir (GS-5734™) in Participants With Severe Coronavirus Disease (COVID-19): Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Safety and Antiviral Activity of Remdesivir (GS-5734™) in Participants With Severe Coronavirus Disease (COVID-19): primary endpoint results, effect estimate with confidence interval, sample-size planning…
- Study to Evaluate the Safety and Efficacy of ATYR1923 (Efzofitimod) In Participants With Severe Pneumonia Related to COVID-19: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Safety and Efficacy of ATYR1923 (Efzofitimod) In Participants With Severe Pneumonia Related to COVID-19: primary endpoint results, effect estimate with confidence interval, sample-size planning…
- Study to Evaluate the Safety and Efficacy of CTP-543 in Adults With Moderate to Severe Alopecia Areata: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Safety and Efficacy of CTP-543 in Adults With Moderate to Severe Alopecia Areata: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration,…
- Study to Evaluate the Safety and Efficacy of Daclatasvir/Sofosbuvir/Ribavirin for 16 Versus 24 Weeks for HCV Genotype 3 Cirrhotics: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Safety and Efficacy of Daclatasvir/Sofosbuvir/Ribavirin for 16 Versus 24 Weeks for HCV Genotype 3 Cirrhotics: primary endpoint results, effect estimate with confidence interval, sample-size…
- Study to Evaluate the Safety and Efficacy of GSK1278863 in Recombinant Human Erythropoietin (rhEPO) Hyporesponsive Hemodialysis-dependent Chronic Kidney Disease Subjects With Anemia: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Safety and Efficacy of GSK1278863 in Recombinant Human Erythropoietin (rhEPO) Hyporesponsive Hemodialysis-dependent Chronic Kidney Disease Subjects With Anemia: primary endpoint results, effect estimate with…
- Study to Evaluate the Safety and Efficacy of High Dose Intravenous Immune Globulin (IVIG) Plus Standard Medical Treatment (SMT) Versus SMT Alone in Participants in Intensive Care Unit (ICU) With Coronavirus Disease (COVID-19): Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Safety and Efficacy of High Dose Intravenous Immune Globulin (IVIG) Plus Standard Medical Treatment (SMT) Versus SMT Alone in Participants in Intensive Care Unit…
- Study to Evaluate the Safety and Efficacy of Liquid Alpha1-Proteinase Inhibitor (Human) in Hospitalized Participants With Coronavirus Disease (COVID-19): Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Safety and Efficacy of Liquid Alpha1-Proteinase Inhibitor (Human) in Hospitalized Participants With Coronavirus Disease (COVID-19): primary endpoint results, effect estimate with confidence interval, sample-size…
- Study to Evaluate the Safety and Efficacy of SPR001 in Subjects With Classic Congenital Adrenal Hyperplasia: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Safety and Efficacy of SPR001 in Subjects With Classic Congenital Adrenal Hyperplasia: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and…
- Study to Evaluate the Safety and Efficacy of Stribild Versus Atripla in Human Immunodeficiency Virus, Type 1 (HIV-1) Infected, Antiretroviral Treatment-Naive Adults: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Safety and Efficacy of Stribild Versus Atripla in Human Immunodeficiency Virus, Type 1 (HIV-1) Infected, Antiretroviral Treatment-Naive Adults: primary endpoint results, effect estimate with…
- Study to Evaluate the Safety and Efficacy of Telavancin in the Treatment of Gram Positive Bloodstream Infections in Cancer Patients: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Safety and Efficacy of Telavancin in the Treatment of Gram Positive Bloodstream Infections in Cancer Patients: primary endpoint results, effect estimate with confidence interval,…
- Study to Evaluate the Safety and Efficacy of the Combination of Tirabrutinib and Idelalisib With and Without Obinutuzumab in Adults With Relapsed or Refractory Chronic Lymphocytic Leukemia (CLL): Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Safety and Efficacy of the Combination of Tirabrutinib and Idelalisib With and Without Obinutuzumab in Adults With Relapsed or Refractory Chronic Lymphocytic Leukemia (CLL):…
- Study to Evaluate the Safety of Novartis MenACWY Conjugate Vaccine When Administered With Routine Infant Vaccinations to Healthy Infants: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Safety of Novartis MenACWY Conjugate Vaccine When Administered With Routine Infant Vaccinations to Healthy Infants: primary endpoint results, effect estimate with confidence interval, sample-size…
- Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamics of BI 655075 (Idarucizumab) Administered Alone or With Dabigatran Etexilate in Japanese Healthy Subjects: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamics of BI 655075 (Idarucizumab) Administered Alone or With Dabigatran Etexilate in Japanese Healthy Subjects: primary endpoint results, effect estimate with…
- Study to Evaluate the Safety, PK, PD and Efficacy of AMG 827 in Adults With Rheumatoid Arthritis: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Safety, PK, PD and Efficacy of AMG 827 in Adults With Rheumatoid Arthritis: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration,…
- Study to Evaluate the Safety, Tolerability and Efficacy of BF-200 ALA (Ameluz®) in the Field-directed Treatment of Actinic Keratosis (AK) on the Extremities and Neck/Trunk With Photodynamic Therapy (PDT) Using a RhodoLED Lamp: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Safety, Tolerability and Efficacy of BF-200 ALA (Ameluz®) in the Field-directed Treatment of Actinic Keratosis (AK) on the Extremities and Neck/Trunk With Photodynamic Therapy…
- Study to Evaluate the Safety, Tolerability, and Immunogenicity of V114 in Healthy Japanese Infants (V114-033): Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Safety, Tolerability, and Immunogenicity of V114 in Healthy Japanese Infants (V114-033): primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety,…
- Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Antiviral Activity of Velpatasvir in Participants With Chronic HCV Infection: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Antiviral Activity of Velpatasvir in Participants With Chronic HCV Infection: primary endpoint results, effect estimate with confidence interval, sample-size planning…
- Study to Evaluate Using Nelfinavir With Chemoradiation for Non-small Cell Lung Cancer: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate Using Nelfinavir With Chemoradiation for Non-small Cell Lung Cancer: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov…
- Study to Explore the Safety, Tolerability and Efficacy of MK-3475 in Combination With INCB024360 in Participants With Selected Cancers: Complete Statistical AnalysisIndependent statistical analysis of Study to Explore the Safety, Tolerability and Efficacy of MK-3475 in Combination With INCB024360 in Participants With Selected Cancers: primary endpoint results, effect estimate with confidence interval, sample-size…
- Study to Find a Safe Dose and Show Early Clinical Activity of Weekly Nab-paclitaxel in Pediatric Patients With Recurrent/ Refractory Solid Tumors: Complete Statistical AnalysisIndependent statistical analysis of Study to Find a Safe Dose and Show Early Clinical Activity of Weekly Nab-paclitaxel in Pediatric Patients With Recurrent/ Refractory Solid Tumors: primary endpoint results, effect estimate with…
- Study to Gather Information on the Acceptability of a New Flavor System With Increasing Levels of 2, 4, 6 g or Higher of Mannitol for PEG 3350 in Subjects Having Infrequent Bowel Movements.: Complete Statistical AnalysisIndependent statistical analysis of Study to Gather Information on the Acceptability of a New Flavor System With Increasing Levels of 2, 4, 6 g or Higher of Mannitol for PEG 3350 in…
- Study to Image the Esophagus Using the OFDI Capsule: Complete Statistical AnalysisIndependent statistical analysis of Study to Image the Esophagus Using the OFDI Capsule: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov results (NCT02204150).
- Study to Investigate Etokimab (ANB020) Activity in Adult Participants With Peanut Allergy: Complete Statistical AnalysisIndependent statistical analysis of Study to Investigate Etokimab (ANB020) Activity in Adult Participants With Peanut Allergy: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov…
- Study to Investigate the Analgesic Efficacy of a Single Dose of AZD1386: Complete Statistical AnalysisIndependent statistical analysis of Study to Investigate the Analgesic Efficacy of a Single Dose of AZD1386: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov…
- Study to Investigate the Influence of Hepatic Insufficiency on the Pharmacokinetics of Grazoprevir (MK-5172-013): Complete Statistical AnalysisIndependent statistical analysis of Study to Investigate the Influence of Hepatic Insufficiency on the Pharmacokinetics of Grazoprevir (MK-5172-013): primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based…
- Study to Investigate the Long Term Survivorship of Coflex: Complete Statistical AnalysisIndependent statistical analysis of Study to Investigate the Long Term Survivorship of Coflex: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov results (NCT02918669).
- Study to Investigate the Long-term Efficacy and Safety of Human-cl rhFVIII in Previously Treated Patients (PTPs): Complete Statistical AnalysisIndependent statistical analysis of Study to Investigate the Long-term Efficacy and Safety of Human-cl rhFVIII in Previously Treated Patients (PTPs): primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and…
- Study to Investigate the Safety and Immunogenicity of a Tetravalent Chimeric Dengue Vaccine in Healthy Volunteers Between the Ages of 1.5 – 45 Years: Complete Statistical AnalysisIndependent statistical analysis of Study to Investigate the Safety and Immunogenicity of a Tetravalent Chimeric Dengue Vaccine in Healthy Volunteers Between the Ages of 1.5 - 45 Years: primary endpoint results, effect…
- Study to Test GSK256073 in Patients With Dyslipidemia: Complete Statistical AnalysisIndependent statistical analysis of Study to Test GSK256073 in Patients With Dyslipidemia: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov results (NCT00903617).
- Study to Test Rizatriptan in the Early Treatment of Acute Migraine (0462-081): Complete Statistical AnalysisIndependent statistical analysis of Study to Test Rizatriptan in the Early Treatment of Acute Migraine (0462-081): primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov…
- Study to Test Sensitivity and Specificity of Passive Wave Pressure Device in Determining Ischemic Stroke: Complete Statistical AnalysisIndependent statistical analysis of Study to Test Sensitivity and Specificity of Passive Wave Pressure Device in Determining Ischemic Stroke: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety,…
- Study to Test the Drug Darolutamide Along With the Drugs Leuprolide Acetate and Exemestane in Patients With Recurrent Ovarian Granulosa Cell Tumors: Complete Statistical AnalysisIndependent statistical analysis of Study to Test the Drug Darolutamide Along With the Drugs Leuprolide Acetate and Exemestane in Patients With Recurrent Ovarian Granulosa Cell Tumors: primary endpoint results, effect estimate with…
- Study to Test the Safety and Efficacy of Padsevonil as Adjunctive Treatment of Focal-onset Seizures in Adult Subjects With Drug-resistant Epilepsy: Complete Statistical AnalysisIndependent statistical analysis of Study to Test the Safety and Efficacy of Padsevonil as Adjunctive Treatment of Focal-onset Seizures in Adult Subjects With Drug-resistant Epilepsy: primary endpoint results, effect estimate with confidence…
- Study to Test the Safety and How Radium-223 Dichloride an Alpha Particle-emitting Radioactive Agent Works in Combination With Pembrolizumab an Immune Checkpoint Inhibitor in Patients With Stage IV Non-small Cell Lung Cancer With Bone Metastases: Complete Statistical AnalysisIndependent statistical analysis of Study to Test the Safety and How Radium-223 Dichloride an Alpha Particle-emitting Radioactive Agent Works in Combination With Pembrolizumab an Immune Checkpoint Inhibitor in Patients With Stage IV…
- Study to Test the Safety and Tolerability of PF-07062119 in Patients With Selected Advanced or Metastatic Gastrointestinal Tumors.: Complete Statistical AnalysisIndependent statistical analysis of Study to Test the Safety and Tolerability of PF-07062119 in Patients With Selected Advanced or Metastatic Gastrointestinal Tumors.: primary endpoint results, effect estimate with confidence interval, sample-size planning…
- Study to Validate the Instructions for Use of TOBI® Podhaler™ in Cystic Fibrosis Patients: Complete Statistical AnalysisIndependent statistical analysis of Study to Validate the Instructions for Use of TOBI® Podhaler™ in Cystic Fibrosis Patients: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based…
- Study Will Evaluate The Safety And Efficacy Of Anidulafungin In Patients With Candidemia Or Invasive Candidiasis: Complete Statistical AnalysisIndependent statistical analysis of Study Will Evaluate The Safety And Efficacy Of Anidulafungin In Patients With Candidemia Or Invasive Candidiasis: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and…