17,261 trials
Candidiasis, Chronic Mucocutaneous
Primary: Clinical Response to Treatment of Mucocutaneous Candidiasis — 4 Participants
Metastatic Colon Cancer · Solid Tumor
Primary: Phase 1: Determine the Maximum Tolerated Dose of Poly-ICLC That Can be Combined With Pembrolizumab — 2 mg
COVID19
Primary: Number of Participants With Inflammatory Marker Reduction of at Least 50% at Any Efficacy Time Point — 5; 8 Participants — p=0.16
Pulmonary Hypertension Secondary · Heart Failure
Primary: Mean Pulmonary Artery Pressure (mPAP) During Submaximal Exercise as Compared Between Placebo and Nitrite — 48.75; 48.68; 56.81; 55.0 mmHg — p=0.20
Alcohol Use Disorder · Alcoholism · Alcohol Dependence
Primary: Alcohol Consumption as Measured by Phosphatidylethanol (PEth) in Blood — -0.406; -0.417; -0.315; 0.250 mikromol/litre
Abnormal Glucose Tolerance · Type 1 Diabetes
Primary: Time From Randomization to Confirmed Abnormal Glucose Tolerance Test — 89.2; 71.6 months
Pancreatic Ductal Adenocarcinoma
Primary: Objective Response Rate — 0 Participants
Non-small Cell Lung Cancer (NSCLC)
Primary: Progression-Free Survival — 14 Participants
Small Fiber Neuropathy
Primary: Denervation of Skin — 0.1; 0.1 percent change — p=0.33
Amyotrophic Lateral Sclerosis (ALS)
Primary: Number of Patients With at Least One Treatment Emergent Adverse Events — 36; 12 Participants
Acute Myeloid Leukaemia
Primary: Dose Limiting Toxicity (DLT) (Phase I - Dose Escalation) — 0; 1; 1 Participants
Systemic Lupus Erythematosus (SLE)
Primary: Percentage of Participants With SLE Responder Index (SRI)-4 Response Status at Week 29 With Reduced Steroid Dose Maintained Between Weeks 17 and 29 — 15; 3; 8; 6…
Hypothyroidism · Thyroid Disease · Euthyroid
Primary: Percentage of Participants With a Sustained TSH Response — 60.76; 75.92 percentage of participants
Alcohol Abstinence
Primary: Percentage of Days Abstinent — 74.7; 50.6 percentage of days abstinent — p=<0.03
Hemophilia A · Hemophilia B
Primary: Number of Participants With Treatment Emergent Adverse Events (TEAEs) and Treatment Emergent Serious Adverse Events (SAEs) — 33; 14; 13; 1 Participants