65,437 trials
Spinal Muscular Atrophy
Primary: Change From Baseline to Week 8 in Forced Vital Capacity (FVC) — -0.02; -0.03; -0.07 liters — p=0.9086
Pheochromocytoma · Paraganglioma
Primary: Number of Participants With Clinical Response (Partial Response + Complete Response) — 5; 0; 5; 2 Participants
Healthy Volunteers
Primary: Maximum Observed Concentration (Cmax) of GDC-0134. — 5.56; 4.45; 2.66; 2.68 uM
A/Vietnam/H5N1 Influenza Virus
Primary: Number of Occurences of Mild, Moderate, or Severe Solicited Local Symptoms During the 7 Days After Each Vaccination. — 34; 41; 34; 34 occurrences
Cocaine Dependence
Primary: Number of Participants Who Are Cocaine Abstinent During the Last 2 Weeks of Treatment (Weeks 8-9), as Assessed by Urine Test — 0; 4; 2 Participants
Hemorrhage · Soft Tissue Bleeding
Primary: Absolute Time to Haemostasis — 4.0; 4.0 Minutes
Treatment of Depression in Adults With Parkinson's Disease (PD)
Primary: Change From Baseline to Week 8 in HAMD-17 (Hamilton Depression Scale -17 Items) Total Score — 19.2; 8.1 score on a scale — p=<0.0001
Heart Failure
Primary: Distance Traveled in Six Minute Walk Test — 306; 296 meters
Non-Hodgkin's Lymphoma
Primary: Overall Survival — 91; 62 percentage of participants
Infection, Human Immunodeficiency Virus · HIV Infections
Primary: Percentage of Participants With Plasma Human Immunodeficiency Virus-1 (HIV-1) Ribonucleic Acid (RNA) Level Below 50 Copies/Milliliter (c/mL) at Week 32 — 95; 94; 91…
ALL · B Cell Lymphoma · Leukemia
Primary: Number of Participants Who Received Preparative Chemotherapy Followed by Cluster of Differentiation (CD)19-Chimeric Antigen Receptor (CAR): CD19 CAR T-cells With < Grade…
Alzheimer Disease
Primary: Acute Safety — 2 participants
Cystic Fibrosis
Primary: Safety and Tolerability as Assessed by Number of Participants With Treatment Emergent Adverse Events (AEs) and Serious Adverse Events (SAEs) — 9; 9; 9; 15 participants
Duchenne Muscular Dystrophy
Primary: Number of Participants With Treatment Emergent Adverse Events (TEAEs), TEAEs Leading to Discontinuation, and Serious Adverse Events (SAEs) — 14; 5; 8; 1 Participants
Esophageal Neoplasms
Primary: Accuracy — 89; 70 Percentage of accuracy