65,437 trials
Ischemic Stroke
Primary: Number of Participants With Adverse Events That Meet Dose-limiting Toxicity (DLT) Criteria Specified in Protocol — 0; 1; 0; 0 Participants
Migraine
Primary: Change From Baseline in the Monthly Average Number of Migraine Days During the 12-Week Period After the First Dose of Study Drug — -2.7; -4.0; -4.2 days — p=<0.0001
Postmenopausal Osteoporosis
Primary: Percentage of Participants With New Vertebral Fracture Through Month 12 — 1.8; 0.5 percentage of participants — p=< 0.001
Anemia in Chronic Kidney Disease Patients Not on Dialysis
Primary: Percentage of Participants in Receipt of 1 or More RBC Transfusions — 24.40; 24.14 Percentage of Participants
Contraception · Pain
Primary: Pain Control With IUD Insertion — 3.606; 3.088; 2.83; 3.382 units on a scale
Multiple Myeloma
Primary: Cmax: Maximum Observed Plasma Concentration for Ixazomib — 37.57 ng/mL
Acute Pain
Primary: Change in Pain Intensity, Baseline to 60 Minutes After Medication Infused — 5.8; 5.2 units on a scale
Glaucoma
Primary: Contrast Sensitivity, Another Means of Testing Vision — 59.4; 74.4; 53.9 units on a scale
Asthma (Part 1) · COPD (Part 2)
Primary: The Number of Participants With Mild Persistent Asthma (Part 1) and COPD (Part 2) With at Least 1 Treatment-emergent Adverse Event — 5; 5; 3; 3 Participants
Schizophrenia
Primary: Change From Baseline to Last Treatment Visit in Clinical Global Impressions-Severity (CGI-S) Scores — -0.2 units on a scale — p=0.078
Diabetes Mellitus Type 2
Primary: Comfortable Gait Speed — 1.2; 1.2 meters per second — p=0.16
Postmenopausal Osteoporosis
Primary: Percent Change From Baseline in Bone Mineral Density (BMD) at the Lumbar Spine — 0.8; 9.6; 9.2 percent change
Depression · Insulin Resistance · Metabolic Syndrome
Primary: Mu-opioid Receptor Binding Potential in Left Nucleus Accumbens, Resting State
Postmenopausal Osteoporosis
Primary: Percent Change From Baseline Through Month 12 in Total Hip Bone Mineral Density (BMD) — -0.6; 2.6 percent change — p=< 0.0001
Type 2 Diabetes Mellitus Who Have Been Examined at a Medical Institution
Primary: Number of Participants Who Experience at Least One Adverse Events — 151; 98; 139 Participants