LEO SAFETY AND EFFICACY OF ESCALATING DOSES OF TWO LEO 43204 FORMULATIONS APPLIED ONCE DAILY FOR TWO CONSECUTIVE DAYS ON FULL FACE OR APPROXIMATELY 250 CM2 (40 IN2) ON THE CHEST IN SUBJECTS WITH ACTINIC KERATOSIS; PART 2: A PHASE 2, MULTICENTRE, RANDOMISED, DOUBLE-BLIND, PARALLEL GROUP, VEHICLE-CONTROLLED, 8-WEEK TRIAL OF LEO 43204 GEL IN SUBJECTS WITH AK (CANADA AND US)

Registry ID
LP0084-1013
Source registry
HEALTH_CANADA
Status
Ongoing
Phase
PHASE2
Study type
INTERVENTIONAL
Sponsor
LEO PHARMA AS
Start date
2014-05-28
Last update
2014-05-22

Conditions

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