University of Houston
Houston, Texas, 77204, United States
NCT Number: NCT06030219
The goal of this study is to assess microbiome changes associated with omadacycline vs. comparators (moxifloxacin or oral vancomycin). Using a phase I study design, healthy volunteers aged 18-40 years will be given a 10-day course of either omadacycline 450 mg days 1 and 2 followed by 300 mg PO once daily, moxifloxacin 400 mg once daily, or oral vancomycin 125 mg given four times daily. Stool will be collected at baseline, daily during therapy, and at two follow-up time periods (days 13-14 and days 30-32). DNA will be extracted from stool and used for qPCR biomass and microbial metagenomic experiments. Results from the study will provide definitive data on the microbiome effects of omadacycline versus comparator antibiotics.
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Notify Me18 year–40 year
All sexes
Interventional
Phase 1
Houston, Texas, 77204, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion. All volunteers will be considered healthy based on medical history
Exclusion. Patients will be excluded if they report any of the following:
10-day course
10-day course
10-day course
Time frame: During dosing and 30 day follow up period
Metagenomic changes (16S rRNA) and qPCR for individual bacterial species
University of Houston
Other
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