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Clinical Trial Summary

The purpose of this study is to evaluate the potential for systemic exposure of aminolevulinic acid (ALA) when applied topically under occlusion, in a maximal use setting in patients with multiple actinic keratoses (AK) involving the upper extremities.


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Pharmacokinetics Study, Intervention Model: Single Group Assignment, Masking: Open Label


Related Conditions & MeSH terms


NCT number NCT02281136
Study type Interventional
Source DUSA Pharmaceuticals, Inc.
Contact
Status Completed
Phase Phase 2
Start date December 2014
Completion date April 2015

See also
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