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Clinical Trial Summary

This is a comparative study to assess bioavailability of a proposed alternate dosage form against the current FDA-approved branded product.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Bio-availability Study, Intervention Model: Crossover Assignment, Masking: Open Label


Related Conditions & MeSH terms


NCT number NCT01448772
Study type Interventional
Source INSYS Therapeutics Inc
Contact
Status Completed
Phase Phase 1
Start date October 2011
Completion date December 2011

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