65,437 trials
Attention-Deficit/Hyperactivity Disorder
Primary: Cmax — 8.07; 10.09; 15.45 ng/mL
Chemotherapy-induced Thrombocytopenia
Primary: Percentage of Subjects Who do Not Require Platelet Transfusion, Dose Reduction in Chemotherapy by 15%, or Chemotherapy Delay by >=4 Days — 57; 29 Participants — p=0.7186
Diabetic Retinopathy · Diabetic Macular Edema
Primary: Development of PDR and/or DME (Whichever Came First) — 27; 75 Eyes
Coronary Artery Disease (CAD)
Primary: Absolute Change From Baseline in Minimum FCT — 21.5; 42.7 µm — p=0.015
Lupus Nephritis
Primary: Change From Baseline in 24-hour Urine Protein to Creatinine Ratio (UPCR) — 0.326; 0.285; 0.305; 0.296 milligram/milligram (mg/mg) — p=0.9052
Fanconi Anemia
Primary: Number of Participant With Neutrophil Recovery — 78 Participants
Neoplasms, Brain
Primary: Incidence of Treatment Emergent Adverse Events (AEs) in Part 1 (Dose Escalation) — 0; 0; 0; 1 Participants
Coronary Artery Disease
Primary: Subjective Image Quality — 5; 5 Score on a Likert scale (0-5) 5=best
Post-Operative Atrial Fibrillation
Primary: Number of Perioperative Complications Associated With AtriClip Placement — 0 perioperative complications reported
Acute Ischemic Stroke
Primary: Functional Outcome as Defined by a mRS of 0-2 at 90 Days Post-procedure — 57 Participants
Overactive Bladder · Urinary Urge Incontinence · Urgency-frequency Syndrome
Primary: Motor or Sensory Response(s) During Lead Placement - by Subject — 107; 109; 3; 1 Participants
Infant, Newborn · Infant, Low Birth Weight · Infant, Small for Gestational Age
Primary: Death or Neurodevelopmental Impairment (NDI) — 44; 46; 27; 28 Participants — p=0.03
Advanced Solid Tumors & Metastatic Squamous Cell Carcinoma of the Head and Neck
Primary: Part A: Danvatirsen With Durvalumab MTDs (Maximum Tolerated Dose) or Recommended Doses for Dose-expansion — 2; 3; 3; 2 mg/kg
Obesity · Weight Loss · CHD - Coronary Heart Disease
Primary: Feasibility - Number of Enrolled Participants — 38 Participants
Refractory Diffuse Large B Cell Lymphoma (DLBCL) · Relapsed Diffuse Large B-Cell Lymphoma · Transformed Follicular Lymphoma (TFL)
Primary: Phase 1 Study: Number of Participants Experiencing Adverse Events (AEs) Defined as Dose Limiting Toxicities (DLTs) — 1 Participants