Outcomes Associated With Tirbanibulin for Large Field Application on the Face in the U.S (CLEAR)
ConditionActinic Keratosis (AK)
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorAvant Health LLC
About this trial
The goal of this observational study is to learn about the effectiveness of tirbanibulin among adult subjects with actinic keratosis (AK) lesions in the face. The main question it aim to answer is:
How does tirbanibulin improve subject's overall appearance of the skin, improve how patient's skin looks, and improve patient's skin texture, in a 57-day observation period.
Participants already taking tirbanibulin as part of their regular medical care for AK will answer online survey questions at the beginning of the study and at Day 57.
Eligibility criteria
Qualifiers
Diagnosed with AK on the face.
Has clinically typical, visible, and discrete 4-12 AK lesions on the face.
Considered as a potential candidate for tirbanibulin (Klisyri®) treatment to manage their AK lesions on the face.
Male or female, aged 18 years and above at the time of initiation of treatment with tirbanibulin.
Disqualifiers
Patients with any dermatological condition of the face that could interfere with clinical evaluations.
Hypertrophic AK lesions, open wounds, or suspected skin cancers within proximity of the treatment area.
Anticipated need for in-patient hospitalization or in-patient surgery within the next 2 months.
Patients unable to comply with the requirements of the study or patients who, in the opinion of the study physician should not participate in the study.
Trial design
Treatments tested in this trial
- Tirbanibulin
Treatment groups
30 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov