12,372 trials
Burns
Primary: Temperature — 18.29; 12.21 Degree Celcius times hours (AUC-T)
Liver Iron Overload
Primary: The Relative Change From Baseline in Liver Iron Content (LIC) After Prolonged Use of Deferasirox — -21.9; -23.1 Percent change
Hepatitis C, Chronic
Primary: Number of Participants With Sustained Virologic Response (SVR) 24 Weeks After the Last Planned Dose of Study Medication - SVR24 Planned — 171; 175; 22 Participants…
Rheumatoid Arthritis
Primary: Change From Baseline in Modified Total Sharp Score (mTSS) From Screening at Week 52 — 1.079; 0.646; 0.359 Score on a scale — p=0.0016
Healthy Subjects
Primary: Percentage of Participants Achieving Predefined Serotype-specific Immunoglobulin G (IgG) Antibody Concentration Greater Than or Equal to (≥) 0.35 Micrograms Per…
Orthomyxoviridae Infection · Influenza · Myxovirus Infection
Primary: Geometric Mean Titers (GMTs) at Baseline and Post-vaccination With Either Fluzone Intradermal or Fluzone Intramuscular Vaccines — 23.50; 25.27; 25.29; 24.84 Titer
Migraine With Aura
Primary: Percentage of Participants Experiencing no Pain at Two Hours Post-treatment — 39; 22 percentage of participants
Fibromyalgia · Sleep Disorders
Primary: Wake After Sleep Onset (WASO) at Weeks 5 and 11 — 70.69; 51.54 Minutes — p=<0.0001
Back Pain
Primary: Pain on the Average, Mean Change From Baseline Days 21-84 (Last Observation Carried Forward [LOCF]) — -1.01; -1.82; -1.92 Units on a scale — p=0.0350
Ulcerative Colitis
Primary: The Number of Participants With Clinical Response at Week 8 — 44 Participants
Multiple Sclerosis
Primary: Percentage of Participants in the Main Subset With Overall Success Using the Avonex Single-Use Autoinjector — 89 percentage of participants
Cardiac Arrest
Primary: Survival to Hospital Discharge. — 8; 11 Participants
Chronic Plaque Psoriasis
Primary: Number of Participants With Relapse Rate (Success or Failure), as Assessed by Psoriasis Area and Severity Index (PASI) Score — 87; 36; 73; 43 Participants
Acquired Immunodeficiency Syndrome · HIV Infection
Primary: Number of Participants With Grade 3 and Grade 4 Adverse Events (AEs) and Serious Adverse Events (SAEs) — 40; 9; 34 Participants
Arthritis, Rheumatoid
Primary: Change From Baseline in Modified Total Sharp Score (mTSS) at Week 52 — 9.82; 5.19; 3.33 Scores on a scale — p=<0.0001