J Drugs Dermatol. 2020 Nov 1;19(11):1093-1100. doi: 10.36849/JDD.2020.5576.
Current field-directed treatments of actinic keratosis (AK), a pre-malignant condition, are often limited by severe local reactions and/or complex treatment. Tirbanibulin, a novel potent anti-proliferative synthetic agent that inhibits tubulin polymerization and Src kinase signalling, is being developed as a convenient, safe, and effective field treatment of actinic keratosis.
A short course of tirbanibulin ointment 1% safely reduces AK lesions.
In the Phase 1 study, 4 treatment cohorts with forearm lesions received tirbanibulin ointment 1% over 25 or 100 cm2 once daily for 3 or 5 days and were evaluated through day 45. In the Phase 2 study, 2 treatment cohorts with face or scalp lesions received tirbanibulin ointment 1% once daily for 3 or 5 days over 25 cm2 and were evaluated through day 57. Lesion reductions, clearance rates, safety, and pharmacokinetics were assessed.
Forearm AK lesions were reduced by day 45 in all Phase 1 cohorts (N=30). Complete AK clearance at day 57 for face/scalp AK lesions in Phase 2 cohorts (N=168) was demonstrated in 43% and 32% of participants of the 5-day and 3-day cohorts, respectively. Adverse reactions were mainly transient mild local erythema and flaking/scaling, pruritus, and pain. Tirbanibulin plasma concentrations were low or undetectable.
Tirbanibulin ointment 1% was well tolerated and active in AK reduction. Based on activity, the 5-day regimen was selected for Phase 3 development. Clinicaltrials.gov: NCT02337205; NCT02838628 J Drugs Dermatol. 2020;19(11):1093-1100. doi:10.36849/JDD.2020.5576THIS ARTICLE HAD BEEN MADE AVAILABLE FREE OF CHARGE. PLEASE SCROLL DOWN TO ACCESS THE FULL TEXT OF THIS ARTICLE WITHOUT LOGGING IN. NO PURCHASE NECESSARY. PLEASE CONTACT THE PUBLISHER WITH ANY QUESTIONS.
光化性角化病(AK)是一种癌前病变,目前的病灶定向治疗常常受到严重的局部反应和/或复杂治疗的限制。替比嘧啶是一种新型强效抗增殖合成剂,可抑制微管聚合和Src 激酶信号传导,作为 AK 的一种方便、安全、有效的病灶治疗方法正在开发中。
短期使用 1%替比嘧啶软膏可安全减少 AK 病变。
在 1 期研究中,4 个前臂病变治疗组每天一次接受 1%替比嘧啶软膏 1%,面积为 25 或 100cm2,持续 3 或 5 天,并在第 45 天进行评估。在 2 期研究中,2 个面或头皮病变治疗组每天一次接受 1%替比嘧啶软膏 1%,面积为 25cm2,持续 3 或 5 天,并在第 57 天进行评估。评估病变减少、清除率、安全性和药代动力学。
所有 1 期研究组的前臂 AK 病变在第 45 天均有减少(N=30)。2 期研究中,面/头皮 AK 病变的第 5 天和第 3 天治疗组分别有 43%和 32%的患者在第 57 天达到 AK 完全清除(N=168)。不良反应主要为短暂的轻度局部红斑和脱屑/鳞屑、瘙痒和疼痛。替比嘧啶的血浆浓度较低或无法检测到。
1%替比嘧啶软膏耐受性良好,对 AK 有活性。基于活性,选择 5 天疗程进行 3 期开发。Clinicaltrials.gov:NCT02337205;NCT02838628 J 皮肤病学杂志。2020;19(11):1093-1100。doi:10.36849/JDD.2020.5576 本文已免费提供。请向下滚动访问本文的全文,无需登录。无需购买。如有任何问题,请与出版商联系。