12,372 trials
Opioid-related Disorders
Primary: Drug's Breakpoint — 1200; 10; 1100; 1200 number of clicks on a mouse
Gaucher Disease
Primary: PAP: Percentage of Participants Who Remained Stable for 52 Weeks During the PAP — 80.4; 83.1 percentage of participants
Systemic Lupus Erythematosus
Primary: Percent of Participants Achieving Systemic Lupus Erythematosus (SLE) Responder Index (SRI) Response Rate at Week 52 for Double-blind Phase. — 40.1; 53.8 Percentage of…
Lung Diseases · Sleep Apnea Syndromes · Sleep
Primary: Effect of CPAP on Neurocognitive Function: E/F Function- SWMT-OMD — 0.035; -0.074; 0.072; 0.018 score on a scale — p=0.0074
Anemia
Primary: Mean Change in Hb Concentration g/dL Between Baseline and the Efficacy Evaluation Period — 1.75 g/dL
HIV-1 Infection
Primary: Percentage of Participants With HIV-1 RNA < 50 Copies/mL at Week 48 as Defined by the FDA Snapshot Analysis — 94.3; 93.0 percentage of participants — p=0.5
Japanese Encephalitis
Primary: Number of Participants With Solicited Injection Site Reactions and Systemic Events Following a Single Primary Dose of a Live Attenuated Japanese Encephalitis Chimeric…
Parkinson's Disease · Multiple Sclerosis
Primary: Maximum Expiratory Pressure (MEP) — 78.6; 75.56; 99.00; 99.38 cm H2O — p=0.899
Hypertension
Primary: Change From Baseline in Mean Seated DBP at Trough After 8 Weeks of the Double-blind Period. — -8.4; -4.5 mmHg — p=<0.0001
Diabetes Mellitus
Primary: Change From Baseline in Glycosylated Hemoglobin (HbA1c) at Week 26 (or Early Termination) — -0.32; -1.23; -1.06; -1.72 percentage of glycosylated hemoglobin — p=< 0.0001
Colorectal Cancer Metastatic
Primary: Percentage of Participants With Adverse Events (AEs) — 100.00; 40.6; 21.1; 9.1 Percentage of participants
Rheumatoid Arthritis
Primary: Percentage of Participants With Adverse Events (AEs) and Serious Adverse Events (SAEs) — 100; 18.2 Percentage of participants
Vitamin D Deficiency
Primary: Change in Serum 25-hydroxy Vitamin D3 — 6.0; -0.8; 10.4; 0.3 ng/ml
Peripheral Spondyloarthritis
Primary: Percentage of Responders According to the Composite Peripheral SpA Response Criteria (PSpARC 40) at Week 12 — 39.3; 19.8; 60.7; 80.2 percentage of participants — p=0.006
Epilepsy
Primary: Number of Participants With Treatment-emergent Serious Adverse Event (SAE) and Adverse Event (AE) — 48; 173 Participants