65,437 trials
Spinal Cord Injuries
Primary: User Ability to Operate the APEX Device — 4; 4 Participants
Atopic Dermatitis
Primary: Change From Baseline in Eczema Area and Severity Index (EASI) at Week 12 — -15.8; -15.8; -17.5; -13.1 score on a scale
Lymphoma
Primary: Phase Ib: Percentage of Participants With Adverse Events (AEs) — 100; 100; 100; 100 percentage of participants
Acromegaly
Primary: Percent Change in Serum Insulin-like Growth Factor-1 (IGF-1) From Baseline to 28 Days After Last Dose — 8.9; -2.8; -7.5 percent change — p=0.306
Anxiety Disorders,Generalized Anxiety Disorder
Primary: Change in Pediatric Anxiety Rating Scale (PARS) Severity Score — -6.38; -7.81 score on a scale — p=0.0281
Visual Acuity
Primary: Overall Vision — 58.37; 53.53 Units on a Scale
Visual Acuity
Primary: Change From Baseline Ocular Comfort (30-Day) — 21.4; 10.0 Units on a scale
Overweight and Obesity
Primary: Visits to Fast Food Restaurants
Recurrent Plasma Cell Myeloma
Primary: Overall Response Percentage — 0.077 percentage of responders
Leptomeningeal Carcinomatosis
Primary: Percentage of Participants With Overall Survival — 44 percentage of participants
Sensorineural Hearing Loss
Primary: Number of Participants With Treatment-emergent Adverse Event(s) (TEAEs) — 2; 3; 5; 6 Participants
Type 1 Diabetes Mellitus
Primary: Percentage of Time of Glucose Concentration Within the Target Range of Greater Than or Equal to (>=) 70 to Less Than or Equal to (<=) 180 Milligrams Per Deciliter…
Juvenile Idiopahtic Arthritis
Primary: Number of Participants With Malignancy: All Periods of Parent and Extension Study — 1 Participants
Surgical Site Infection
Primary: Occurrence of Superficial Surgical Site Infection — 11; 21; 107; 128 Participants
Multiple Sclerosis, Chronic Progressive
Primary: Number of Participants With Treatment-emergent Adverse Events — 18 Participants