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Clinical Trial Summary

The primary objective of this study is to assess the safety and tolerability of STMC-103H compared to placebo in allergic subjects who are otherwise healthy.


Clinical Trial Description

This is a first-in-human trial of this live biotherapeutic product. The primary objective is to assess safety and tolerability in allergic subjects who are otherwise healthy, with twice daily dosing in descending age groups. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03819881
Study type Interventional
Source Siolta Therapeutics, Inc.
Contact Elizabeth Chesnut
Phone 404-803-0358
Email echesnut@sioltatherapeutics.com
Status Recruiting
Phase Phase 1
Start date October 10, 2018
Completion date November 2019