17,261 trials
Respiratory Syncytial Virus Infections
Primary: Area Under the Viral Load-time Curve (VL-AUC) of RSV — 0.00; 96.65 h*log10 PFU/mL
Depression · Opioid-use Disorder · Opioid Abuse
Primary: Percentage of Individuals Completing Informed Consent — 34 Participants
Diabetes Mellitus, Type 2 · NASH - Nonalcoholic Steatohepatitis
Primary: Number of Treatment-Emergent Adverse Events — 0; 2 Adverse Events
Dry Eye Disease
Primary: Least Squares Mean Change From Baseline in Pre-CAE (Controlled Adverse Environment) Ocular Discomfort Score (ODS) on a Visual Analogue Scale at Day 28 — -15.3; -11.0…
Non-Small Cell Lung Cancer (NSCLC)
Primary: Objective Response Rate (ORR) in Cohort A — 33.3 percentage of participants
Gastroparesis
Primary: Change From Baseline in Average Nausea Severity — -1.25; -0.73 score on a scale (change from baseline) — p=.0099
Glioma, Malignant · Surgery · Seizures
Primary: Peritumoral HFO Rate — 2.5; 1.4 HFOs per minute
Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN) · Acute Myeloid Leukemia (AML)
Primary: MTD (Stage 1) — 12; 12; 16 µg/kg/day
Mantle Cell Lymphoma · Non-Hodgkin's Lymphoma
Primary: Progression-free Survival (PFS) — NA years
Head and Neck Squamous Cell Carcinoma
Primary: Progression-free Survival at ≤12 Months — 71; 83 percentage of patients
Anhedonia · Major Depressive Disorder
Primary: Change in Anhedonia Severity, as Measured by Change in DARS Score From Baseline to Day 57 — 17.4; 13.5 units on a scale — p=0.8663
Rheumatoid Arthritis
Primary: Change in Disease Activity Score — -0.95; -0.91; -1.06; -1.15 score on a scale
Alzheimer Disease
Primary: Safety: Treatment-emergent Adverse Events and Serious Adverse Events for All Randomized Subjects Who Received Any Study Medication — 15; 13; 4; 4 number of events
Hepatitis B, Chronic
Primary: Percentage of Participants With Hepatitis B Surface Antigen (HBsAg) Seroclearance at Week 72 Without Restarting NA Treatment — 0.0; 0.0 Percentage of participants
Melanoma
Primary: Number of Participants With Dose Limiting Toxicities (DLT) [Phase I] — 1 Participants