65,437 trials
Coronary Artery Disease
Primary: Major Adverse Cardiac and Cerebrovascular Event (MACCE) — 23; 10; 3; 1 participants — p=0.80
Fecal Incontinence
Primary: Adverse Events — 223; 7 Number of events
Parkinson's Disease
Primary: Modified Fatigue Impact Scale (MFIS) — 12.92; 12.69 units on a scale — p=0.81
Chronic Obstructive Pulmonary Disease (COPD)
Primary: The SD1 Index, a Nonlinear Index of Heart Rate Variability (HRV)That Represents the Parassimpatetic Activity. — 3.7; 2.8; 7.1; 2.5 miliseconds
Functional Limitation
Primary: Knee Extension Strength — 20.4; 19.5 kg
Lubricating Agents
Primary: Number of Subjects With Irritation Score of "0" at Baseline and One Week — 35; 35; 35; 35 Participants
Breast Cancer
Primary: Number of Patients With Progression-free Survival (PFS) at 24 Weeks — 67; 68 Participants
Open-Angle Glaucoma · Ocular Hypertension · Pigment Dispersion Glaucoma
Primary: Mean Change From Baseline in IOP at Week 12 in Subjects Using Ganfort® at Baseline — 20.0; -3.8 millimeters mercury (mmHg)
Epilepsy
Primary: Seizure Frequency — 0.655; 0.435; 0.631 Seizures per Day
Adenocarcinoma of the Pancreas · Recurrent Pancreatic Cancer · Stage IV Pancreatic Cancer
Primary: Objective Response Rate as Measured by RECIST Criteria — 3; 6 participants
Prostate Cancer
Primary: All Cause Mortality — 171; 183 Participants
Sarcoma
Primary: Number of Patients With Complete or Partial Response Assessed by RECIST Criteria — 63 percentage of participants
Healthy
Primary: Mean Difference Changes From Baseline Versus Placebo in QTcNi Intervals From Time-Matched Analysis by Largest Time Point — 7.0; 13.0; 12.6 msec — p=<0.001
Schizophrenia
Primary: Mean Clinical Global Impression Severity Score (CGI-S) From Baseline Through End of Study- - Safety Population. — 2.6; 1.0; 2.3; 1.1 units on a scale
Ischemic Heart Disease
Primary: Short-term End Point — 61; 77 participants