Efficacy and Safety of Cryotherapy Followed by Tirbanibulin Ointment for Actinic Keratosis on the Scalp and Forehead

Trial statusNot yet recruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity Hospital, Lille

About this trial

The aim of the study is to evaluate the efficacy and safety of a combined approach of cryotherapy and tirbanibulin for the treatment of actinic keratosis of the scalp and forehead, repeated every 4 months. A higher rate of complete response is expected with this combination compared to cryotherapy alone, as well as a better response with repeated treatment cycles.

Eligibility criteria

Qualifiers

Subject over 18 years old presenting with ≥ 8 typical actinic keratoses (AK), clinically visible or palpable, grade I or II, with at least 4 AK per hemiscalp,

Participants who, in the investigator's judgment, are in good general condition (ECOG ≤ 2),

The AK must be distributed in 2 non-overlapping areas, and of similar grades,

Patient capable of understanding and adhering to the study visit schedule and other protocol requirements,

Disqualifiers

Clinically atypical and/or rapidly evolving actinic keratoses (AK) in the treatment area, and grade 3 AK according to Olsen classification,

Located somewhere other than the scalp and/or forehead,

Within 5 cm of a wound that is not fully healed or a lesion suspicious for carcinoma,

Prior treatment with tirbanibulin,

Trial design

Treatments tested in this trial

  • Cryotherapy + Tirbanibulin

Treatment groups

59 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators