12,372 trials
Multiple Sclerosis
Primary: Number of Participants Experiencing Adverse Events (AEs) — 668; 775; 776 Participants
Primary Myelofibrosis · Post-Polycythemia Vera · Myelofibrosis
Primary: Spleen Volume Response Rate (RR) — 35.8; 6.0 Percentage of Participants — p=<0.0001
Age-related Macular Degeneration
Primary: Distribution of the Last Interval With no Disease Activity up to Week 32 - Study Eye — 141; 73; 131; 147 Participants — p=<0.0001
Sexually Transmitted Diseases · Gonorrhea · Chlamydia
Primary: Percentage of Study Successes in the EVO100 and Placebo Treatment Groups — 684; 696 Participants
Progressive Keratoconus
Primary: Difference Between Treatment Groups in the Change From Baseline to Month 6 in Kmax — -0.3; 0.6 Diopters — p=0.0004
Pelvic Floor Disorders
Primary: Changes of Levator Hiatal Area During Valsava — 20.64; 20.35; 22.35; 21.41 Cm2 — p=0.086
Leber Hereditary Optic Neuropathy
Primary: Ocular Adverse Events (AEs) — 5; 1 eyes
Strongyloides Stercoralis Infection
Primary: Cure Rate Against Strongyloides Stercoralis — 94.8; 99.4 percentage of participants
Type 1 Diabetes Mellitus
Primary: Absolute Change After 12 Weeks From Baseline in Mean HbA1c With Addition of Dapagliflozin Compared to Placebo. — 0; -0.66 % HbA1c
Ankylosing Spondylitis
Primary: Percentage of Participants Who Achieved an ASAS40 (Assessment of SpondyloArthritis International Society Criteria) — 40.85; 22.94 percentage of participants — p=<0.0001
Neuroborreliosis, Borrelia Burgdorferi
Primary: Difference in Composite Clinical Score From Inclusion to Six Months After Ended Treatment — 6.4; 6.4 units on a scale
Keratosis, Actinic
Primary: Number of Participants Categorized by Local Tolerability Score by Visit for Each Individual Signs (Erythema, Flaking/Scaling, Crusting, Swelling…
Type 1 Diabetes
Primary: HbA1c (%) — 7.92; 7.48; 7.45; 7.58 Percent of Hemoglobin (%)
Nausea · Vomiting
Primary: Complete Response (CR) — 4; 11; 4 Participants
Carcinoma, Hepatocellular
Primary: Overall Survival — 8.7; 6.8 months