17,261 trials
Gastrointestinal Stromal Tumor
Primary: Progression-free Survival (PFS) — 3.9 months
Diabetic Neuropathy, Painful; Diabetic Neuropathies
Primary: Brief Pain Index - Item 5, Average Daily Pain Score (Range 0-10) Higher Values Indicate Worse Pain — 4.24; 4.41; 4.27 Average daily pain score — p=0.5695
Keratoconjunctivitis Sicca
Primary: Change of Corneal Fluorescein Staining of the Inferior Cornea Region. — -1.00; -0.78; -0.78 units on a scale (Likert)
Migraine
Primary: Percentage of Participants Reporting Pain Freedom (PF) at 2 Hours Post-Dose — 8.9; 5.6; 14.8; 21.4 percentage of participants
Migraine
Primary: The Number of Treated Subjects Who Became Pain-free (International Headache Society Grade of 0 = no Pain) by Observation Time Point. — 12; 7 participants
Asthma
Primary: Change in FEV1 — -0.40; 0.69; -0.59 percentage of change
Prostatic Neoplasms
Primary: Number of Participants With Treatment-emergent Adverse Events (AEs) — 41 Participants
Infections, Streptococcal
Primary: Number of Subjects With Any and Grade 3 Solicited General Symptoms and With Solicited General Symptoms Related to Vaccination - Primary Phase of the Study — 82; 76; 72…
Tuberculosis
Primary: Percentage of Participants With Negative Lowenstein Jensen Cultures at Week 8 — 85; 94; 96 percentage of participants w/LJ cx con
Rheumatoid Arthritis
Primary: Change From Baseline in Disease Activity Score of 28 Joints Using C-Reactive Protein (DAS28 [CRP]) Score at Day 85 — 5.78; 5.73; 5.91; 5.67 units on a scale — p=<0.001
Kaposi's Sarcoma
Primary: Localization — 5 participants
Epilepsy · Tuberous Sclerosis Complex
Primary: Reduction in Seizure Frequency — 60 percentage
Multiple Myeloma · Stage I Multiple Myeloma · Stage II Multiple Myeloma
Primary: Maximum Tolerated Dose (Phase I) — 0; 0; 0; 3 participants
Malignant Glioma · Recurrent Glioblastoma
Primary: Progression Free Survival (PFS) at 6 Months — 0.29; 0.23 Months — p=0.26
Extrahepatic Bile Duct Cancer · Gallbladder Cancer
Primary: Stratum-specific (R0 and R1) 2-year Overall Survival — 67; 60 percentage of participants