Trials that use: Interim analysis / alpha spending
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11,819 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 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 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 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, 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 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 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 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…
- Study to Evaluate the Efficacy and Safety of APL-2 in Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH): Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Efficacy and Safety of APL-2 in Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH): primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and…
- Study to Evaluate the Efficacy and Safety of Aripiprazole Administered With Lithium or Valproate Over 12 Weeks in the Treatment of Mania in Bipolar I Disorder: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Efficacy and Safety of Aripiprazole Administered With Lithium or Valproate Over 12 Weeks in the Treatment of Mania in Bipolar I Disorder: primary endpoint…
- Study to Evaluate the Efficacy and Safety of Benralizumab in Adult Patients With Mild to Moderate Persistent Asthma: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Efficacy and Safety of Benralizumab in Adult Patients With Mild to Moderate Persistent Asthma: primary endpoint results, effect estimate with confidence interval, sample-size planning…
- Study to Evaluate the Efficacy and Safety of Camidanlumab Tesirine (ADCT-301) in Patients With Relapsed or Refractory Hodgkin Lymphoma: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Efficacy and Safety of Camidanlumab Tesirine (ADCT-301) in Patients With Relapsed or Refractory Hodgkin Lymphoma: primary endpoint results, effect estimate with confidence interval, sample-size…
- 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 Erenumab (AMG 334) in Migraine Prevention: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Efficacy and Safety of Erenumab (AMG 334) in Migraine Prevention: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based…
- Study to Evaluate the Efficacy and Safety of Eribulin Mesylate Administered Biweekly (Q2W) for Participants With Human Epidermal Growth Factor Receptor 2 (HER2)-Negative Metastatic Breast Cancer: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Efficacy and Safety of Eribulin Mesylate Administered Biweekly (Q2W) for Participants With Human Epidermal Growth Factor Receptor 2 (HER2)-Negative Metastatic Breast Cancer: primary endpoint…
- Study to Evaluate the Efficacy and Safety of FX006 in Patients With Hip Osteoarthritis: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Efficacy and Safety of FX006 in Patients With Hip Osteoarthritis: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based…
- Study to Evaluate the Efficacy and Safety of Hyoscine Butylbromide Tablets for the Treatment of Occasional or Recurrent Episodes of Gastric or Intestinal Spasm-like Pain or Discomfort: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Efficacy and Safety of Hyoscine Butylbromide Tablets for the Treatment of Occasional or Recurrent Episodes of Gastric or Intestinal Spasm-like Pain or Discomfort: primary…
- Study to Evaluate the Efficacy and Safety of Leronlimab for Mild to Moderate COVID-19: Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Efficacy and Safety of Leronlimab for Mild to Moderate COVID-19: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based…
- Study to Evaluate the Efficacy and Safety of RZ402 in Diabetic Macular Edema (DME): Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Efficacy and Safety of RZ402 in Diabetic Macular Edema (DME): primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based…
- 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 Of Tofacitinib In Patients With SJS/TEN: Complete Statistical AnalysisIndependent statistical analysis of Study To Evaluate The Efficacy Of Tofacitinib In Patients With SJS/TEN: primary endpoint results, effect estimate with confidence interval, sample-size planning illustration, and safety, based on ClinicalTrials.gov results…
- 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 Pharmacokinetics of PT001, PT003, and PT005 Following Chronic Dosing (7 Days) in Patients With Moderate to Very Severe Chronic Obstructive Pulmonary Disease (COPD): Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Efficacy, Safety and Pharmacokinetics of PT001, PT003, and PT005 Following Chronic Dosing (7 Days) in Patients With Moderate to Very Severe Chronic Obstructive Pulmonary…
- Study to Evaluate the Efficacy, Safety and Tolerability of an Oral Aripiprazole/Escitalopram Combination Therapy in Participants With Major Depressive Disorder (MDD): Complete Statistical AnalysisIndependent statistical analysis of Study to Evaluate the Efficacy, Safety and Tolerability of an Oral Aripiprazole/Escitalopram Combination Therapy in Participants With Major Depressive Disorder (MDD): primary endpoint results, effect estimate with confidence…