The purpose of this study is to investigate the efficacy of LAS41005 in comparison to placebo and to LAS106521 in actinic keratosis (AK).
To investigate as primary objective: * Superiority to placebo and non-inferiority to LAS106521 measured by histological clearance of one predefined target lesion; To investigate as secondary objective: * Superiority to LAS106521 * Improvement of treated lesions (lesion response) * Assessment of tolerability and safety by physicians global assessment score (PGA, PGT) * Patient's assessment of tolerability and efficacy and patient's compliance
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
470
Histological status of AK target lesion
Time frame: Day 140
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Almirall Facility Site#37
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