Clinical Evaluation of Lyral® Dose Response Study

Status Completed

Clinical Trial Summary

The purpose of this study is to determine optimal allergen dose as the lowest concentration eliciting positive reactions in 70-90% of subjects. Frequency of positive, negative, doubtful and irritant reactions, and concordance with a corresponding reference allergens will be captured.

Clinical Trial Description

This is a single-center, randomized study to compare the diagnostic performance and safety of ascending doses (0.10 mg/cm², 0.20 mg/cm² and 0.40 mg/cm²) of hydroxyisohexyl 3-cyclohexene carboxaldehyde (Lyral®) in 20 adult subjects with a past positive patch test to Lyral® or Fragrance Mix 2. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02028182
Study type	Interventional
Source	Allerderm
Contact
Status	Completed
Phase	Phase 2
Start date	February 2013
Completion date	June 2013

View Details

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