Condition: Celiac Disease · Sponsor: Nielsen Fernandez-Becker
The goal of this clinical trial is to learn about the safety of a single dose of HB-2121 in adults with suspected celiac disease. It will also look at how the drug affects the small intestine. The main questions it aims to answer are: * What side effects do participants have after receiving HB-2121? * How does the drug interact with the small intestine in people with suspected celiac disease? 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 four hours before their standard-of-care esophagogastroduodenoscopy * 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
This description comes directly from the study's public registry record.
Joaquin Tabera · (650) 334-1308 · jtabera7@stanford.edu
Marissa Dobry · (313) 320-2240 · mdobry@stanford.edu
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| Stanford University | Stanford, California, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07377565