4,901 trials
Opioid-use Disorder
Primary: Median Cmax of Naltrexone (After 1st Dose) — 14.10 ng/mL
Human Cancers
Primary: Serious Adverse Events (SAEs) and Non-serious Adverse Events (AEs) Considered to be at Least Possibly Related to MOv18 IgE — 0; 5; 2; 0 Participants
Uterine Fibroids
Primary: Changes in Epigallocatechin Gallate (EGCG) — 5.8; 256.3; 86.4 nM — p=0.112
HIV Infections
Primary: Cohort 1: Area Under the Plasma Concentration-time Curve (AUC) From Time Zero Extrapolated to Infinity (AUC [0-inf]) of DTG, ABC and 3TC Following Administration of…
Healthy
Primary: Number of Participants With Treatment-related Adverse Events (AEs) Assessed by Physical Examinations — 0; 0 Participants
Pulmonary TB
Primary: Local Injection Site Reactogenicity — 22; 21 participants
Dementia · Healthy
Primary: Number of Participants Who Received a Cognitive Screening — 5; 11 Participants
Nicotine Dependence
Primary: Changes in Liking of E-cigarette Overall — 14.2; 5.3; 11.9; 2.2 score on a scale — p=0.01
Solid Tumor
Primary: Maximum Observed Concentration (Cmax) of Pamiparib in Plasma for Part A — 1970; 1820 ng/mL
Squamous Cell Carcinoma of the Head and Neck · Carcinoma of the Head and Neck
Primary: Detection of Tumor in Lymph Nodes by 18F-FDG and 89Zr-panitumumab Labeling — 0; 4; 0; 0 Lymph Nodes
HIV Infection
Primary: Number of Participants With Adverse Events — 1; 2; 3; 0 Participants
Facioscapulohumeral Muscular Dystrophy
Primary: Number of Participants Who Experienced an AE — 14 Participants
Chronic Kidney Disease
Primary: Maximum Plasma Concentration (Cmax) of Apraglutide — 39.5; 65.8 ng/mL
HIV-1 Infection
Primary: Number of Participants w/ at Least One ≥ Grade 3 Adverse Event That is Possibly or Definitely Related to Vorinostat (VOR) or HIV-specific T Cell (HXTC) — 0 Participants
Healthy
Primary: Pharmacokinetic Outcome Measures [AUC0-inf] for Part 2 — 910.9; 897.7; 926.3 day*μg/mL