65,437 trials
Influenza
Primary: Number of Participants With Solicited Injection Site and Systemic Adverse Events — 1; 2; 1; 3 participants
Psoriasis
Primary: Duration of Drug-Free Interval Prior to Treatment Cycle 2 — 12.6 weeks
Methamphetamine or Cocaine Dependence
Primary: Change in Psychostimulant-positive Urines Over Time — .6; .41; .79; .25 proportion of psychostimulant-pos urines — p=0.05
Diabetes · Hypertension · Obesity
Primary: Change in Flow-mediated Dilation From Baseline to 4 Hours — 0.16; -3.2; -0.9; -2.4 percent change in diameter
Ascites · Cirrhosis
Primary: Number of Participants With Worsening Ascites (Increase in Number of Paracentesis Procedures to Remove 2 Liters of Ascites Fluid) — 0 participants
Healthy
Primary: AUC0-∞ for Empagliflozin — 2780; 2870; 1110; 1070 nmol*h/L — p=0.0000
Composite Restorations · Tooth Lesions
Primary: Retention — 100; 100; 100; 97 percentage of restorations
Kaposi´s Sarcoma
Primary: Number of Participants With Complete Response — 1; 3 participants
Healthy
Primary: Area Under the Concentration-time Curve of the Analyte in Plasma Over the Time Interval From 0 Extrapolated to Infinity, Empagliflozin — 2810; 2580; 2760; 2570 nmol*h/L…
Acute Myeloid Leukemia
Primary: Overall Response Rate of GTI-2040 Combined With HiDAC in Refractory or Relapsed AML — 3; 4 participants
Sarcoma · Gastrointestinal Stromal Tumors
Primary: 2-year Relapse Free Survival Rate — 93.6 percentage of participants
Adenocarcinoma of the Rectum · Mucinous Adenocarcinoma of the Colon · Recurrent Colon Cancer
Primary: Severe Adverse Event (SAE) Rate — 2; 2 participants
Fatigue Syndrome, Chronic
Primary: Change From Baseline in Multidimensional Fatigue Inventory (MFI)--General Fatigue Subscale Score — -3.3; -1.8 units on a scale — p=0.23
Headache · Migraine
Primary: Number of Participants Who Reported a 50% or Greater Reduction in Pain at 15 Minutes as Measured on the 100mm Visual Analog Scale — 48.8; 41.3 percentage of participants
Diffuse Large B-cell Lymphoma
Primary: Overall Objective Response Rate During Treatment Cycle 1 — 57.1; 100.0; 30.8 percentage of participants