65,437 trials
Neoplasms
Primary: Maximum Tolerated Dose (MTD) of BAL101553 — 70 mg/m²
Fall · Risk Reduction
Primary: Number of Participants With Reported Falls — 37; 34; 29; 24 Participants
Type 2 Diabetes Mellitus
Primary: Mean ApoB Concentration Before and After Evolocumab — 75.9; 35.3 mg/dL — p=<0.001
Open Angle Glaucoma · Ocular Hypertension
Primary: Mean IOP — 21; 22.9; 20.2; 21.9 mmHg
Healthy Volunteers · Anti-Bacterial Agents · Methicillin-Resistant Staphylococcus Aureus
Primary: Safety and Tolerability Evaluation — 1; 6; 1; 3 Participants
Prostate Cancer · Bladder Cancer · Non-small Cell Lung Cancer
Primary: Number of Patients With Dose Limiting Toxicities (DLTs) and Number of Patients With Adverse Events — 0; 0; 0; 3 Participants
Respiratory Syncytial Virus Prophylaxis
Primary: Number of Subjects Reporting Adverse Events Through 30 Days After Dosing — 3; 5; 3; 6 Participants
Sleep Disturbance · Sleep Deprivation · Sleep
Primary: Number of Caregiver-child Participants Who Complete All Intervention Procedures Following Enrollment (Retention Rate) — 13; 2 Participants
Glaucoma · Glaucoma, Open-Angle · Glaucoma, Neovascular
Primary: Intraocular Pressure (IOP) — 15.2 millimeters of mercury (mm Hg)
Meibomian Gland Dysfunction · Evaporative Dry Eye Disease
Primary: Least Squares Mean Change From Baseline in Meibomian Gland Score (MGS) at Month 12 — 17.4; 17.8 score on a scale
Schizophrenia · Alcohol Use Disorder
Primary: Number of Participants With Independent Adjudication Committee (IAC) Adjudicated Event of Exacerbation of Disease (EEDS) — 25; 29; 87; 88 Participants — p=0.746
Colorectal Cancer
Primary: Median Progression Free Survival (mPFS) — 8.8 months
Subarachnoid Hemorrhage
Primary: Tolerability as Assessed by the Number of Participants Who Stop Study Medication Due to Adverse Event Possibly Associated With Study Drug — 1; 1 Participants
Hemophilia A
Primary: Change of the Median Factor VIII (FVIII) Activity — 4.1 IU/dL
Linkage to Care · Homelessness · Substance Use Disorder
Primary: Substance Use Care — 37; 7 Participants