65,437 trials
Burn Injury · Skin Graft
Primary: Part A: Number of Participants With Healing — 3; 21; 2; 22 Participants
Essential Hypertension Complicated by Type 2 Diabetes Mellitus
Primary: Change in Insulin Resistance Index (HOMA-R) From Baseline at the End of the Treatment Period (Week 12) — -0.23; 0.22 HOMA-R Score
Epilepsy
Primary: Incidence of Treatment Emergent Adverse Events (TEAEs) During Evaluation Period — 78.9; 71.4 percentage of subjects
Prostate Cancer · Bone Metastases
Primary: Number of Subjects With Dose Limiting Toxicity (DLT) — 0; 0; 0; 0 subjects
Cannabis Dependence · Alcohol Dependence · Cannabis Use Disorder
Primary: Change From Week 0 in Cannabis Use Using Urinary CN-THCCOOH Levels at Week 8 — 198.3; 55.9 ng/mg
Dermatomyositis · Polymyositis
Primary: Specific Aim 1: Number of Subjects Meeting IMACS Preliminary Definition of Improvement (DOI). — 7 Participants
Colorectal Cancer
Primary: Number of Dose-limiting Toxicities (DLTs) — 0; 1 DLT
Schizophrenia · Schizoaffective Disorder
Primary: PANSS Total — 77.9; 80 units on a scale — p=0.02
Lung Cancer
Primary: 8 Week Progression-Free Survival Rate (i.e. Disease Control Rate) — 20 Participants
Overweight · Obesity
Primary: Body Weight in Pounds — 207.4 pounds
Uveal Melanoma
Primary: Number of Participants With Complete Response (CR) — 13; 0 Participants
Osteosarcoma Metastatic
Primary: The Study Medication Was to be Considered Effective if the Population Response Rate Was Found to be Greater Than 20% and Individuals Who Demonstrated a CR or PR or Whose…
Alzheimer's Disease
Primary: One-card Learning (OCL) Measurement Over 12 Weeks of Treatment — 0.954; 0.942; 0.822; 0.969 Score on a scale
Chronic Hepatitis C Infection
Primary: Percentage of Participants With Sustained Virologic Response 12 Weeks Post-treatment (SVR12) — 96.4 percentage of participants
Diabetic Macular Edema
Primary: Number of Participants With Non-severe Ocular Adverse Events — 9; 5; 4; 3 Participants — p=<0.05