drugset / Trial / NCT01527734

Comparison Study of Liquid and Lyophilized Formulations of Subcutaneous Tetrodotoxin (TTX) in Healthy Volunteers

NCT01527734 ↗

Phase 1 Completed 44 enrolled Wex Pharmaceuticals Inc.
RandomizedCrossoverQuadruple-blindScreening

Summary

The study design is a randomized, double-blind, placebo-controlled, parallel-group, dose comparison with a open-label, crossover, formulation comparison.

Timeline

Start
2011-12
Primary completion
2012-01
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject Tetrodotoxin Small molecule 15 ug Subcutaneous
Subject Tetrodotoxin Small molecule 30 ug Subcutaneous

Indications

No indication recorded.