65,437 trials
Major Depressive Disorder
Primary: Change in Hamilton Depression Rating Scale (HAM-D 17) Score — -11.7; -5.3; -15.7; -6.1 units on a scale — p=0.04
Encephalitis · Japanese Encephalitis
Primary: Percentage of Participants With Japanese Encephalitis Seroprotection Following a Single Dose of JE-CV — 2.6; 100.0; 88.2; 90.0 Percentage of participants
Alzheimer's Disease
Primary: Mean Change From Baseline in the 4-Item Agitation/Aggression Subscale of the Neuropsychiatric Inventory (NPI-4 A/A) at Week 12 — -5.4; -6.2 units on a scale
Osteoporosis · Prostate Cancer
Primary: Freedom From Any Bone Fracture (FABF) Rate at Three Years — 98.0; 97.4 percentage of participants — p=0.95
Tobacco Use Disorder
Primary: Abstinence — 10; 11 Participants
Chronic Idiopathic Constipation
Primary: Overall Responder 9/12 Weeks — 18.6; 16.8; 19.0; 10.7 % of Overall Responder 9/12 weeks
Iron Deficiency Anemia (IDA)
Primary: Maximum Serum Concentration (Cmax) — 157; 310 µg/mL
Asthma
Primary: Maximum Plasma Concentration (Cmax) of Mepolizumab for Part A — 12.8188; 16.3412; 10.1960 Microgram (ug) per mL
Wounds and Injuries
Primary: Number of Inpatient Operating Room Debridements — 9; 13; 52; 41 Participants — p=0.6770
Dysfunctional RVOT Conduits in Patients With Congenital Heart Defects
Primary: Number of Subjects With Acceptable TPV Hemodynamic Function At 6 Months — 25 Participants
Post Thrombotic Syndrome · Deep Vein Thrombosis · Venous Stasis Syndrome
Primary: Median Optimal Electrical Stimulation Intensity Level for Largest Benefit in Relief of Symptoms — 32 mirco coulombs (0 to 50)
Type2 Diabetes
Primary: [11C]5-hydroxy-tryptophan Uptake in the Pancreas — 0.17; 0.21; 0.20; 0.23 % of injected dose — p=0.5875
Smoking Cessation
Primary: Percentage of Participants With 30-day Abstinence — 18.0; 23.4; 22.1; 18.7 percentage of participants
Calcinosis
Primary: Change in Dermatomyositis-associated Calcinosis of a Single Lesion by Assessing Its Severity as Measured by a Difference in Physician Calcinosis Visual Analog Scales…
Smallpox
Primary: To Determine the Number of Participants With Adverse Events — 134; 30 Participants