17,261 trials
Lymphoma
Primary: Progression Free Survival — 79 percentage of patients progression free
Pain · Bladder Cancer · Breast Cancer
Primary: Number Who Reached a Safe Dose — 8 participants
Multiple Myeloma and Plasma Cell Neoplasm
Primary: Hematologic and Organ Response — 11; 7; 18 participants
Diabetic Neuropathy, Painful
Primary: Time to Efficacy Failure (TTEF) - Primary Responders — NA; NA Days
MELAS Syndrome
Primary: Mean Change in Cerebral Lactate Concentration (as Measured by Magnetic Resonance Spectroscopy) — -0.09; 0.16; -0.49 IU
Bladder Cancer
Primary: Treatment Completion Rate — 67; 53 percentage of participants
Cancer of Head · Cancer of Head and Neck · Cancer of Neck
Primary: Probability of Progression-free Survival (PFS) at 2 Years — 70 percentage of participants
Pulmonary Arterial Hypertension
Primary: Plasma Estradiol (E2) Level — -40; -4 % change from baseline
Locally Recurrent · Metastatic Breast Cancer ( HER2 Negative)
Primary: Objective Response Rate (ORR) — 28.6 Percentage of participants
Lung Cancer
Primary: PERCIST Partial Metabolic Response — 6 participants
Head and Neck Cancer
Primary: Participants With Mucositis and Hematological Toxicities With the Addition of Radioprotector Amifostine — 16 participants
Prostate Cancer
Primary: Number of Participants Progression Free at 1 Year — 13 participants
Chronic Obstructive Pulmonary Disease (COPD)
Primary: Change From Baseline in Normalized Forced Expiratory Volume in One Second (FEV1) Area Under the Curve (AUC) for 0-12 hr — 0.170; 0.219; 0.230; 0.075 Liters — p=<0.0001
Major Depressive Disorder
Primary: Change in Montgomery-Asberg Depression Rating Scale (MADRS) Total Score From Baseline to Day 15 — 35.6; 33.3; 36.8; 35.4 Units on a scale — p=< 0.001
Hepatitis B, Chronic
Primary: Efficacy: Percent Change From Baseline in Serum Hepatitis B Surface Antigen (HBsAg) Titer at End of the Combination Treatment (Week 48) — 59.13 percent change