drugset / Trial / NCT04534153
Excipient Effect on Drug Absorption in Humans
Phase 0
Completed
12 enrolled
University of California, San Francisco
Food and Drug Administration (FDA) · collab
RandomizedCrossoverDouble-blindBasic science
Summary
The purpose of this study is to determine if sodium lauryl sulfate (SLS), a non-drug ingredient commonly added in drug products, affect absorption of drugs that are given together with the ingredient. Investigators want to find out if drug absorption is different in people taking the drug alone compared to people taking the drug with low and high amounts of sodium lauryl sulfate at the same time.
Timeline
- Start
- 2023-01-31
- Primary completion
- 2025-06-18
- Completion
- 2025-08-18
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Fexofenadine | Unknown | 120 mg | Oral |
Indications
No indication recorded.