The goal of this clinical trial is to learn about the safety of a single dose of HB-2121 in adults. It will also look at how the body processes the drug. The main questions it aims to answer are: * What side effects do participants have after receiving HB-2121? * How much HB-2121 is in the blood over time? Researchers will follow participants for 30 days after receiving HB-2121 to understand how the drug behaves in the body and how safe it is. Participants will: * Receive one oral dose of HB-2121 * Attend 4 in-person clinic visits for checkups, lab tests, and monitoring * Complete 2 remote visits that include safety lab assessments * Fill out a short daily questionnaire for 7 days about symptoms and health status
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
18
HB-2121 taken once orally.
Stanford University
Stanford, California, United States
Frequency and severity of adverse events during the study window
Adverse events (AEs) will be recorded and assessed for severity using the Common Terminology Criteria for Adverse Events (CTCAE) v5.0.
Time frame: From dosing through 30 days post-dose
Peak Plasma Concentration (Cmax) of HB-2121
Blood samples will be collected at specified time points to determine the peak plasma concentration (Cmax) of HB-2121 following administration.
Time frame: Pre-dose, and at 15, 30, 60, 120, 180, 240, and 360 minutes, and 1 day after dosing.
Time to Peak Plasma Concentration (Tmax) of HB-2121
Time to reach the maximum plasma concentration (Tmax) of HB-2121 will be determined from blood sample data collected at specified time points.
Time frame: Pre-dose, and at 15, 30, 60, 120, 180, 240, and 360 minutes, and 1 day after dosing.
Area Under the Plasma Concentration-Time Curve (AUC) for HB-2121
The area under the plasma concentration versus time curve (AUC) for HB-2121 will be calculated using plasma concentration data from collected blood samples.
Time frame: Pre-dose, and at 15, 30, 60, 120, 180, 240, and 360 minutes, and 1 day after dosing.
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