This is a Phase 2 study evaluating the safety, tolerability, systemic exposure, and activity of topical ATx201 GEL (2% and 4%) treatment for 1, 2, or 5 days in outpatients with primary nonbullous or bullous impetigo.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
210
ATx201 GEL
Vehicle
AntibioTx Investigational Site
Bloemfontein, South Africa
AntibioTx Investigative Site
Boksburg, South Africa
AntibioTx Investigative Site
Incidences of Adverse Events and Laboratory Parameters
incidences of adverse events reports and changes in significant laboratory parameters
Time frame: 14 days
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Claremont, South Africa
AntibioTx Investigative Site
Durban, South Africa
AntibioTx Investigative Site
eMkhomazi, South Africa
AntibioTx Investigative Site
Germiston, South Africa
AntibioTx Investigative Site 2
Johannesburg, South Africa
AntibioTx Investigative Site
Johannesburg, South Africa
AntibioTx Investigative Site
Kraaifontein, South Africa
AntibioTx Investigative Site
Mpumalanga, South Africa
...and 6 more locations