65,437 trials
Primary Open Angle Glaucoma
Primary: Change in Superior Retinal Capillary Blood Flow (% Zero Pixels) — -0.026; 0.011 % zero pixels — p=0.0016
Multiple Myeloma
Primary: Number of Participants With Adverse Events During NKAE Treatment — 2 participants
Partial Epilepsy
Primary: Change in Epworth Sleepiness Scale Score From Baseline to Visit 4 — -1.2; -1.1 Units on a scale — p=0.027
Cystic Fibrosis
Primary: Part A: Observed Plasma Concentration of Lumacaftor (LUM) and Ivacaftor (IVA) at Hour 4 Post-dose (C4h) on Day 1 — 15200; 1920 nanogram per milliliter (ng/mL)
Heart Failure
Primary: Lead Complication-free Rate at 6 Months — 96.04; 98.75; 96.21 Survival Probability (%)
Sleep Initiation and Maintenance Disorders · Depression
Primary: Percent of Participants With Depression Remission — 36.0; 43.8 percentage of participants in arm
Opioid-Related Disorders
Primary: Subjective Opioid Withdrawal Scale Score (SOWS) — 16; 4; 24 units on a scale
Scleroderma, Systemic · Scleroderma, Diffuse · Scleroderma, Limited
Primary: Digital Skin Microvascular Blood Flow Measured by Laser Doppler Imaging (LDI) Before Cold Stimulus — 260.0; 246.3 perfusion units
Non-small Cell Lung Cancer
Primary: Overall Response Rate (ORR) by Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST 1.1) in Strongly PD-L1 Positive Participants — 27.3 Percentage of…
Subjects Desiring Lip Augmentation
Primary: Change From Baseline in Evaluating Investigator's Assessment of Lip Fullness on a 5-Point Scale — 1.2; 1.1; 1.1; 1.0 Scores on a Scale
Epilepsy
Primary: Adverse Events — 126; 26 Number of adverse events
Heart Valve Diseases
Primary: Thromboembolism/Thrombosis — 0; 2.7; 2.4; 1.5 percentage of participants/patient-year
Hemophilia A
Primary: Number of Participants With Inhibitory Antibodies to Factor VIII (FVIII) — 0; 0; 0 participants
MDS
Primary: Percentage of Participants With at Least One Red Blood Cell (RBC) Transfusion During the Double-blind Treatment Period — 59.2; 36.1 percentage of participants — p=0.008
Recurrent Prostate Cancer
Primary: Patients With PSA <4 ng/mL at the End of the Study — 17 participants