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Clinical Trial Summary

The objectives of this enabling study are to characterize the wheal and flare responses over time following skin challenges with ascending concentrations of Substance P. This will be a 2-part study: Part 1 will aid in the understanding of the wheal and flare responses following Substance P. Part 2 will investigate the variability of the responses. Participants may be enrolled into Part 1 or Part 2, not both.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04676763
Study type Interventional
Source GlaxoSmithKline
Contact
Status Completed
Phase N/A
Start date March 2, 2021
Completion date July 21, 2021

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