65,437 trials
Epilepsy
Primary: Maximum Drug Concentration (Cmax) — 9469; 9867; 15067; 17309 ng/mL
Diseases, Metabolic · Insulin Sensitivity
Primary: Flow Mediated Dilation — 10.3; 8.9; 9.2; 9.1 percentage of brachial artery diameter
Epilepsy
Primary: Cmax - Peak Plasma Concentration — 14286.790; 18677.265; 15055.632; 14974.79 ng/mL
Breast Cancer
Primary: Time to Progression — 7.4 months
Cardiomyopathy
Primary: Sustained Ventricular Fibrillation — 38; 35 participants
Chronic Low Back Pain
Primary: Symptoms of Chronic Lower Back Pain as Measured With the Visual Analog Scale (VAS) — 26.32; 20.45 percentage of change from baseline to 5
Allergic Asthma · Atopic Dermatitis · Allergic Rhinitis
Primary: Number of Participants With Treatment-Emergent Adverse Events (TEAEs) and Treatment-Emergent Serious Adverse Events (TESAEs) — 8; 2; 2; 1 participants
Psoriatic Arthritis
Primary: Mean Change From Baseline in Disease Activity Score (DAS)28 — -1.7; -1.9; -1.9; -2.0 score on a scale
Melanoma
Primary: Determine Dose Limiting Toxicities (DLTs) of VELCADE When Administered in Combination With IFN-α-2b to Patients With Metastatic Malignant Melanoma. — 3; 1 toxicities
Post-anesthesia Recovery · Orientation
Primary: Re-orientation Time — 24.5; 19.5 minutes
Chronic Hepatitis C Virus
Primary: Percentage of Participants With Sustained Virologic Response 12 Weeks After Discontinuation of Therapy (SVR12) — 94.0; 93.1; 96.3 percentage of participants — p=<0.001
Type 2 Diabetes · Hypertension
Primary: Changes in Systolic Blood Pressure During Initial Intralipid Infusion — 23; 13 mmHg
Chronic Pain
Primary: Numeric Rating Scales of Pain Over Past Week (11 Point Likert Scale) — 4.66; 3.80; 4.92; 3.30 units on a scale
Epilepsy
Primary: Number of Adverse Events Reported — 10; 7; 7 Number of adverse events reported
Multiple Myeloma
Primary: Number of Participants With Adverse Events (AE) During the Treatment Phase — 327; 268; 256; 177 participants