65,437 trials
Cancer
Primary: Number of Adverse Events From Escalating Doses of NGR-hTNF in Combination With a Fixed Dose of Doxorubicin — 59; 142; 67; 101 Adverse event
Infections, Streptococcal
Primary: Number of Subjects With Bacterial Aetiology, Assessed by Culture Growth, From Bronchoalveolar Lavage (BAL) Fluid Samples — 141; 49; 1; 58 Participants
Primary Immunodeficiency
Primary: AUC in the IV Phase and SC Phases: Steady-state AUC of Total IgG Over a Regular Dosing Interval — 207921.5; 213141.4 h*mg/dL
Coronary Disease
Primary: Proportion of Subjects With Device Related Adverse Events. — 0 Proportion of subjects
Contraception
Primary: The Number of On-treatment Pregnancies (With + 2-day Window) Per 100 Woman-years of Exposure (Pearl Index) in Subjects Aged 18 to 35 Years, Inclusive, at the Time of…
Respiratory Tract Infections · Urinary Tract Infections
Primary: Number of Participants With Adverse Events — 10; 4; 6; 10 Participants — p=0.05
Stable Angina
Primary: Percentage of Participants With Major Adverse Cardiac Events(MACE) — 1.72; 6.86 percentage of participants
Strabismus · Reflex, Oculocardiac · Hydroxyzine
Primary: Heart Rate-1 — 114.4; 125.8; 122.3 beats per minute
Actinic Keratoses
Primary: Change in Treatment Symptoms — 3.9; 0.5; 0.37 score on a scale
Cerumen Impaction of Both Ears
Primary: Percentage of Ears That Showed Change in Visualization of the Tympanic Membrane (Ear Drum) Following 15 or 30 Minutes of Using the Test Product — 53.3; 85.7 percentage…
Pharmacokinetic Bioequivalence Study in Human Healthy Volunteers
Primary: Pharmacokinetic (PK) Endpoints: Pegfilgrastim C[Max] — 474.269; 425.578 ng/mL
Irritable Bowel Syndrome With Diarrhea
Primary: Change in the Bowel Movements (Stool Frequency) Between the 'Intervention' Group and the 'Placebo' Group Over the Study Period. — .46; .21 bowel movements/day
Squamous Cell Carcinoma of the Head and Neck
Primary: Change From Baseline in 18F-EF5 Standardized Uptake Values (SUV) — 1.49 SUVmax
Small Cell Lung Cancer
Primary: Antitumour Activity Defined as Progression Free Survival (PFS) — 3.2 months
First Trimester Abortion · Virtual Reality
Primary: Number of Participants Able to Use VR Device Throughout the Entire Duration of First Trimester Surgical Abortion. — 6 participants