65,437 trials
Psoriatic Arthritis
Primary: Percentage of Participants Achieving American College of Rheumatology 20 Index (ACR20) — 19.5; 53.3; 48.0 Percentage of Participants — p=<0.001
Huntington's Disease
Primary: Number of Participants With Treatment-Emergent Adverse Events (AEs) or Serious Adverse Events (SAEs) — 18; 14; 1; 1 participants
Hyperlipidemia
Primary: Percent Change From Baseline in Fasting Low Density Lipoprotein Cholesterol (LDL-C) at Week 12 — 2.4; -52.0; -32.6 percent (%) change — p=<0.001
Mild to Moderately Active Ulcerative Colitis
Primary: Number of Subjects With a Reduction in the Disease Activity Index of >3, or Clinical Remission. — 10; 0 Participants — p=0.03
Acute Pain
Primary: Part A: Weighted Mean Change From Baseline in Pain Intensity Over the First 8 Hours Post-Dose Using VAS — -3.8; -47.4; -12.7 mm
Phase 1 Sickle Cell
Primary: Number of Participants With Potentially Clinically Important (PCI) Change From Baseline in Vital Signs — 0; 0; 0; 2 participants
Snoring
Primary: Snoring Severity Scale — -4.1 units on a scale — p=< 0.0001
Hepatobiliary Disease
Primary: The Total Blood Loss — 376.73; 339.81 ml
Cerebral Palsy · Postural; Defect
Primary: Sitting Assessment Scale — 12.56; 15.06 units on a scale — p=0.001
Asthma
Primary: Salmeterol Protected Methacholine Challenge PC20 — 1.8; 1.7 mg/ml on log base 2 scale
Infections, Meningococcal
Primary: Percentage of Subjects With Human Serum Bactericidal Activity (hSBA)≥1:4 — 84; 84; 84; 7 Percentage of subjects
Japanese Encephalitis
Primary: Percentage of Participants With JE Seroprotection Before and Following a Booster Dose of IMOJEV Given One Year After Primary Immunization — 93.5; 100.0 Percentage of…
Tinnitus
Primary: Change From Baseline in Tinnitus Reaction on the Tinnitus Handicap Questionnaire Scores (0-100) at 4 Months — 22.03; 24.9; 23.7; 25.4 units on a scale — p=>0.05
Obesity · Type 2 Diabetes
Primary: Pancreatic Fat Content — 9.6; 13.0 Percentage of fat
Hepatitis C Infection · Hepatitis C Virus
Primary: Percentage of Participants Who Achieve Sustained Virologic Response 12 Weeks Post-treatment (SVR12) — 97.6 percentage of participants