17,261 trials
Veisalgia
Primary: Efficacy of Side Effect Prevention Using the Acute Hangover Scale — 6.7; 4.7; 7.8; 6.8 score on a scale
Type 2 Diabetes Mellitus
Primary: Change From Baseline to 6 Weeks in Mean 24-Hour Systolic Blood Pressure — 2.79; 0.53 mmHg — p=<.001
Symptomatic Focal Vitreomacular Adhesion
Primary: Release of Vitreo Macular Adhesion (VMA) by Optical Coherence Tomography (OCT) — 4; 0 Participants
Prostate Cancer
Primary: (Phase I) Maximum Tolerated Dose — 4000 mg
Cancer
Primary: Number of Participants With Dose Limiting Toxicity (DLT) — 0; 0; 1; 2 Participants
Unresected Stage IIIb to IVM1c Melanoma
Primary: Odds Ratio of Baseline Intratumoral CD8+ Cell Density and Objective Response Rate — 1.11 ratio — p=0.387
Acute Myeloid Leukemia · Myelodysplastic Syndrome
Primary: Number of Subjects With Unacceptable Toxicity — 1 Participants
Esophageal Cancer
Primary: Determine Pathologic Complete Response — 9 Participants
Anovulation
Primary: Ovulation Rate in Cycle 1 — 64.9; 30.4; 36.8; 35.9 percentage of subjects
Advanced Melanoma · Cancer
Primary: Response Rate (ie, the Percentage of Subjects With a Confirmed Complete or Partial Response) — 0; 0; 0; 0 percentage of participants
Exudative Age-related Macular Degeneration
Primary: Percent of Eyes With Severe Ocular Adverse — 0; 0; 0 percentage of participants
Heart Failure
Primary: Skeletal Muscle Bioenergetics- Polymerase Chain Reaction (PCR) — 12.04; 11.91; 11.79; 11.76 Relative Expression
Prostate Cancer
Primary: Number of Participants With Immune Response Following Treatment — 6; 5 Participants
Ewing's Sarcoma /Peripheral Neuroectodermal Tumor (PNET) · Rhabdomyosarcoma · Leiomyosarcoma
Primary: Percentage of Participants With Progression-Free Survival (PFS) at 12 Weeks — 27.3; 12.5; 25.4; 50.0 percentage of participants
Breast Cancer
Primary: Percentage of Participants With an Objective Overall Response — 6.1 percentage of participants