drugset / Trial / NCT04290039
Sublingual vs IV Atropine Bioavailability Study
Phase 1
Completed
15 enrolled
Biomedical Advanced Research and Development Authority
Rho, Inc. · collab
RandomizedCrossoverOpen-labelTreatment
Summary
This randomized, three-sequence, three-period, phase 1 study is designed to assess the bioavailability and pharmacokinetics (PK) of sublingually administered atropine sulfate ophthalmic solution 1% USP (at 0.5 mg and 1.0 mg; test) compared to atropine sulfate injection administered IV (1.0 mg; reference).
Timeline
- Start
- 2020-01-04
- Primary completion
- 2020-02-02
- Completion
- 2020-02-08
Publications
- Background Rajpal S, Ali R, Bhatnagar A, Bhandari SK, Mittal G. Clinical and bioavailability studies of sublingually administered atropine sulfate. Am J Emerg Med. 2010 Feb;28(2):143-50. doi: 10.1016/j.ajem.2008.10.025.
- Background Pai S, Ghezzi EM, Ship JA. Development of a Visual Analogue Scale questionnaire for subjective assessment of salivary dysfunction. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2001 Mar;91(3):311-6. doi: 10.1067/moe.2001.111551.
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Atropine | Other / unclassified | 0.5 mg | Subcutaneous |
| Comparator | Atropine | Other / unclassified | 1 mg | Subcutaneous |