17,261 trials
Obesity, Morbid · Bariatric Surgery · Adolescent
Primary: Enrollment Rate — 19 percentage of participants
HIV Infections
Primary: Proportion of Participants Experiencing a Grade 3 or Higher Adverse Event (AE) or Premature Discontinuation Due to an AE (Regardless of Grade) That is Related To Step 2…
Multiple Myeloma
Primary: Overall Response Rate — 74.5 Percentage of Participants
Postural Orthostatic Tachycardia Syndrome
Primary: Change From Baseline to Week 24 in the COMPASS 31 (2-week Recall Version) — -14.369; -15.957 score on a scale
Lung Cancer, Nonsmall Cell · Lung Cancer · Lung Cancer, Small Cell
Primary: Number of Participants With Treatment Emergent Adverse Events — 18 Participants
Nicotine Addiction · E-Cig Use · Quitting Smoking
Primary: Biochemically Confirmed 7-day Point-prevalence Cigarette Abstinence — 16; 26; 16; 16 Participants
Oropharynx Cancer
Primary: The Percentage of Patients With Local Regional Recurrence (LRR) of Disease — 2; 3 percentage of participants
Spinal Cord Injuries · Tetraplegia · Paraplegia
Primary: Change in Muscle Mass Using Dual X-ray Absorptiometry (DXA) — -183.00; 1434.00 grams
Advanced Solid Tumors
Primary: Part A: Number of Participants With Dose-limiting Toxicities (DLTs) Based on Common Terminology Criteria for Adverse Events (CTCAE) — 0; 0; 0; 2 Participants
Eosinophilic Esophagitis
Primary: Change From Baseline in the Peak Esophageal Intraepithelial Eosinophil Count at Week 4 (Mean) — -9.2; -31.6; -7.8 eosinophil count per high power field
Uncontrolled Hypertension · Chronic Kidney Diseases
Primary: Change From Baseline in Mean Seated Systolic Blood Pressure (SBP) of Pooled CIN-107 and Placebo — -15.22; -7.15 Millimeters of mercury (mmHg) — p=0.003
Major Depressive Disorder
Primary: Number of Participants Who Dropped-out — 0 Participants
Dry Eye Disease · Dry Eye Syndrome
Primary: Stage 1: Number of Participants With Adverse Events — 5; 1; 4; 2 Participants
Discoid Lupus Erythematosus
Primary: Mean Severity of Disease as Measured by the Investigator's Global Assessment — 1.4 score on a scale
Prevention of COVID-19
Primary: Antibody Titre Increase 14 Days After Study Vaccination Dose. — 100; 100; 78.46; 87.22 percentage of participants