17,261 trials
Prostate Cancer
Primary: To Evaluate the Efficacy of Bevacizumab Plus Erlotinib — 9; 1; 2; 7 participants
Chronic Obstructive Pulmonary Disease
Primary: Forced Expiratory Volume in One Second (FEV1) Area Under Curve (AUC) 0-24 Hours on Day 14 — 1.827; 1.664 Liters
Estrogen Receptor-positive Breast Cancer · Progesterone Receptor-positive Breast Cancer · Recurrent Breast Cancer
Primary: Clinical Benefit Rate — 44; 41 percentage of participants
Rheumatoid Arthritis
Primary: Response to Intravenous Canakinumab and Oral Methotrexate (MTX) Compared to MTX Alone as Determined by 50% Improvement in Symptoms According to the American College of…
Carcinoid Tumors
Primary: Symptom Control (Diarrhea/Flushing) Using a Patient Symptom Diary — 3; 9; 32 participants
Gout
Primary: Core Study: Mean Number of Gout Flares Per Participant — 0.5; 0.4; 0.2; 0.4 Gout flares
Schizophrenia
Primary: Number of Subjects With an Adverse Events in a One Year Open Label Lurasidone Study — 59 participants
Leukemia · Myelofibrosis
Primary: Number of Participants With Objective Response — 0; 0; 6 Participants
Leukemia · Chronic Myelogenous Leukemia · Chronic Myeloid Leukemia
Primary: Number of Participants With Complete Response — 3 Participants
Macular Degeneration
Primary: Summary of Adverse Events — 57; 16; 47; 4 participants
Acute Ischemic Stroke
Primary: Number of Participants With Symptomatic Intracerebral Hemorrhage — 0 participants
Spinal Muscular Atrophy
Primary: Safety Labs
Epilepsy · Sleep Apnea · Obstructive Sleep Apnea
Primary: CPAP Adherence/Tolerance as Measured by Proportion of Nights Used — 0.74; 0.66 proportion of nights used (total nights — p=0.26
Sickle Cell Disease · Iron Overload · Hemolytic Anemia
Primary: The Number of Participants With Adverse Events (AEs) in the First 24 Weeks of Treatment — 30; 17; 30; 8 participants
Systemic Mastocytosis
Primary: Number of Participants With Objective Response — 0 Participants