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Safety and tolerability of tirbanibulin ointment 1% treatment on 100 cm2 of the face or scalp in patients with actinic keratosis: A phase 3 study.
Bhatia, Neal; Lain, Edward; Jarell, Abel; DuBois, Janet; Tamarit, Maria Luisa; Falques, Meritxell; Kiyasova, Vera; Padullés, Laura; Otero, Raquel; Blauvelt, Andrew.
Afiliación
  • Bhatia N; Therapeutics Clinical Research, San Diego, California.
  • Lain E; Austin Institute for Clinical Research, Pflugerville, Texas.
  • Jarell A; Sanova Dermatology, Austin, Texas.
  • DuBois J; allCUTIS Research, Inc. Portsmouth, New Hampshire.
  • Tamarit ML; DermResearch, Inc., Austin, Texas.
  • Falques M; Almirall, Sant Feliu de Llobregat, Spain.
  • Kiyasova V; Almirall, Sant Feliu de Llobregat, Spain.
  • Padullés L; Almirall, Sant Feliu de Llobregat, Spain.
  • Otero R; Almirall, Barcelona, Spain.
  • Blauvelt A; Almirall, Sant Feliu de Llobregat, Spain.
JAAD Int ; 17: 6-14, 2024 Dec.
Article en En | MEDLINE | ID: mdl-39268198
ABSTRACT

Background:

Tirbanibulin is approved for actinic keratosis (AK) field treatment up to 25 cm2. However, AK often affects larger areas; thus, AK treatments for larger fields are needed.

Objective:

Evaluate the safety and tolerability of tirbanibulin when applied to a field of approximately 100 cm2.

Methods:

Phase 3, multicenter, open-label, single-arm study among adult patients having a treatment field on the face or balding scalp of approximately 100 cm2 with 4-12 AKs. Patients received tirbanibulin to cover the treatment field once daily (5 consecutive days). Safety was assessed by evaluating treatment emergent adverse events and tolerability by composite score of 6 local tolerability signs (LTS).

Results:

A total of 105 patients were included. The most common LTS were erythema (96.1%) and flaking/scaling (84.4%), being mostly mild-to-moderate severity, and resolved/returned to or close to baseline by Day 29. The only severe LTS were erythema (5.8%) and flaking/scaling (8.7%). Most frequent treatment emergent adverse events were application site pruritus (10.5%) and application site pain (8.6%). Mean total number of AKs decreased from 7.7 AKs at baseline to 1.8 AKs at Day 57. Mean percent of change (reduction) from baseline in lesion count was 77.8% at Day 57.

Limitations:

No control group. No long-term follow-up.

Conclusion:

Safety and tolerability profiles in patients treated with tirbanibulin up to 100 cm2 were consistent with those previously reported over smaller field. Tirbanibulin could be used on a larger field (>25 cm2).
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: JAAD Int Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: JAAD Int Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos