This phase I/IIa study has an open-label, First-in-Human (FIH), single center design to assess the safety, pharmacokinetics (PK) and pharmacodynamics (PD) of multiple doses of topically applied CLS003 in healthy subjects with cutaneous warts.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
12
Centre for Human Drug Research
Zernikedreef 8, Netherlands
Area under the plasma concentration versus time curve (AUC) of CLS003
Time frame: 7 days
Number of participants with adverse events
Time frame: 7 days
Peak Plasma Concentration (Cmax) of CLS003
Time frame: 7 days
Time to reach Cmax (Tmax)
Time frame: 7 days
Pharmacodynamic effects of topically applied CLS003 on wart morphology and HPV viral load
Time frame: 7 days
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