drugset / Trial / NCT07063823
A First-in-human Study to Evaluate the Safety and Tolerability of HB-2121 as a Diagnostic for Celiac Disease
Phase 1
Completed
18 enrolled
Nielsen Fernandez-Becker
Stanford's Innovative Medicines Accelerator · collab
Non-randomizedSequentialOpen-labelDiagnostic
Summary
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
Timeline
- Start
- 2025-08-26
- Primary completion
- 2026-04-07
- Completion
- 2026-04-07
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | HB-2121 | Diagnostic / imaging agent | 50 mg | Oral |
| Subject | HB-2121 | Diagnostic / imaging agent | 150 mg | Oral |
| Subject | HB-2121 | Diagnostic / imaging agent | 250 mg | Oral |