65,437 trials
Healthy
Primary: Number of Participants With Adverse Event (AE) and Severe Adverse Event (SAE) — 0; 0; 4; 0 participants
Paroxysmal Supraventricular Tachycardia
Primary: Number of Participants With Adverse Events for Self-administered Etripamil NS Outside of the Clinical Setting. — 324 Participants
Coronavirus Disease-2019 (COVID-19) Prevention
Primary: Groups 1, 2, 3, 4, 5 and 6: Number of Participants With Solicited Local Adverse Events (AEs) at 7 Days Post-dose 1 — 13; 16; 17; 11 Participants
Duchenne Muscular Dystrophy
Primary: Number of Participants With Adverse Events (AEs) — 4 Participants
Alzheimer's Disease
Primary: Concentration of Angiotensin Converting Enzyme (ACE 1) — 4043.15; 4028.17; 3836.31; 3305.21 ng/mL
Prostate Cancer
Primary: Prostate Specific Antigen (PSA) Screening Rates — 77.8; 76.7 Percentage of participants
Opioid-use Disorder
Primary: Retention in Treatment on MAT for 6 Months After Enrolling in the Study — 34; 27 Participants
THROMBOLYSIS
Primary: Ordinal Modified Rankin Scale (mRS) Score at Day 90 — 35; 31; 38; 30 Count of participants
CVA (Cerebrovascular Accident)
Primary: Change in Gait Speed — 0.15; 0.075; 0.127 meters/second
Primary Hyperoxaluria Type 1 (PH1) · Primary Hyperoxaluria Type 2 (PH2) · Kidney Diseases
Primary: AUC From Day 90 To Day 180, Based on Percent Change From Baseline in 24-Hour Uox — 3507.4; -1664.4 Percent change in 24-hour Uox AUC — p=<0.0001
Diabetic Retinopathy
Primary: Single-rising Dose (SRD) Part - The Number of Patients With Dose Limiting Events (DLEs) From Drug Administration Until Day 8 — 0; 0; 0 Participants
Hypertension
Primary: Time From Randomization to Composite Primary Outcome — 1.5; 1.5 Years — p=0.45
Sars-CoV-2 Infection · COVID-19
Primary: Standard Diagnostic Test Outcomes for BinaxNOW at Home Testing as Compared to Nasal Swab PCR — 100; 99; 75; 100 kappa value in percentage — p=0.0015
Cervical Cancer
Primary: Cervical Cancer Screening — 198; 289 individuals screened — p=<0.001
Atrial Fibrillation · Aortic Valve Stenosis
Primary: Composite of All-cause Mortality, Stroke and Bleeding — 60; 64 Participants