The aim of this study is to determine the efficacy, safety and tolerability of either a once or twice daily topical application of LAS41007 compared to a twice daily application of LAS106521 in the treatment of actinic keratosis.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
100
Once daily, topical application
Twice daily, topical application
Twice daily, topical application
Investigational Site
Hamburg, Germany
Histological clearance of one pre-selected target lesion
Time frame: Day 120
Complete clinical clearance of all target lesions in the treatment areas
Time frame: Day 120
Physician's Global Tolerability Assessment (PGT)
Time frame: Day 120
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