17,261 trials
Prostate Cancer · Metastatic · Hormone Refractory
Primary: Prostate Specific Antigen (PSA) Response — 17; 29 Participants
Thyroid Cancer
Primary: Objective Response Rate — 6 Participants
Colorectal Cancer
Primary: Number of Patients With an Objective Disease Progression Event — 20; 24; 24 Participants
Advanced Breast Cancer
Primary: Number of Patients With a Disease Progression Event — 24; 18 Participants
Colorectal · Cancer
Primary: Number of Patients With an Objective Disease Progression Event — 23; 27; 24 Participants
Lung Cancer
Primary: Number of Participants Whose Response Allowed Them to Proceed to Chemoradiation — 38 participants
Neuralgia, Postherpetic
Primary: Change From Baseline in the Mean 24-hour Average Pain Intensity (API) Score at the Last Week of Each Treatment Period Using Last Observation Carried Forward (LOCF) Data…
Neuralgia, Postherpetic
Primary: Change From Baseline in the Mean 24-hour Average Pain Intensity (API) Score at the End of Maintenance Treatment (EOMT) Using Last Observation Carried Forward (LOCF) Data…
Breast Cancer
Primary: Tumor Response Rate — 26.6; 29.5; 0.0; 3.3 percentage of participants
Anxiety Disorders
Primary: Change From Baseline in the Hamilton Rating Scale for Anxiety (HAM-A) Total Score — -10.9; -11.1; -11.5; -10.9 Units on scale
Schizophrenia
Primary: Number of Participants With Adverse Events — 19; 22; 18 participants
Iron Overload · Hereditary Hemochromatosis
Primary: Absolute Change of Serum Ferritin From Baseline to the End of Extension, by Dose Cohort (Extension Per-protocol Population) — -389.1; -610.5; -571.6 µg/L
Diabetic Peripheral Neuropathy · Neuralgia
Primary: Placebo vs. Active Comparison of the Change From Average Pain at Baseline to Average Pain at 4 Weeks. — 1.64; 2.12 units on a scale — p=0.083
Attention Deficit Hyperactivity Disorder
Primary: The Number of Chromosomal Aberrations Per 100 Cells Excluding Gaps at Baseline and at the End of Treatment i.e Day 84 (Week 12) — 1.05; 0.75; 0.53; 0.41 number of…
Depressive Disorder, Major Depressive Disorder
Primary: Number of Participants With Adverse Events AEs) and Serious Adverse Events (SAEs) — 13; 15; 1; 0 participants