Expanding the Scope of PROTACs: Opportunities and Challenges in Topical Delivery

Proteolysis-targeting chimeras (PROTACs) have emerged as a novel therapeutic modality primarily through systemic administration. Recently, their topical use has drawn increasing attention, offering a promising strategy to achieve localized protein degradation while minimizing systemic toxicity. This miniperspective highlights key advances in the development of topical PROTACs, exemplified by <b>AH-001</b> and <b>GT20029</b>, androgen receptor degraders, both in clinical trials for androgenetic alopecia, with <b>GT20029</b> also evaluated for acne. We discuss emerging degraders that target clinically relevant proteins, including JAK kinases and BET family members, with applications extending beyond dermatology to pulmonary and ocular diseases and even cosmetic use. Innovative strategies, such as liposomes and microneedle systems, are also enabling effective local delivery. Despite this progress, topical PROTACs face some challenges, such as optimizing the stability, tissue penetration, and selective target engagement under physiological conditions. We conclude by outlining strategic directions that could accelerate the clinical translation of this emerging therapeutic modality.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2025-11-19
DOI
https://doi.org/10.1021/acs.jmedchem.5c01911
Citations
2
Primary Topic
Protein Degradation and Inhibitors
Type
article
Field-Weighted Citation Impact
1.61
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article

Expanding the Scope of PROTACs: Opportunities and Challenges in Topical Delivery

Tracey Pirali, Rita Maria Concetta Di Martino, Laura Gioiello
2 citations
Journal of Medicinal Chemistry
Protein Degradation and Inhibitors
1.61
article

Expanding the Scope of PROTACs: Opportunities and Challenges in Topical Delivery

Tracey Pirali, Rita Maria Concetta Di Martino, Laura Gioiello
article en
2 citations

Abstract

Proteolysis-targeting chimeras (PROTACs) have emerged as a novel therapeutic modality primarily through systemic administration. Recently, their topical use has drawn increasing attention, offering a promising strategy to achieve localized protein degradation while minimizing systemic toxicity. This miniperspective highlights key advances in the development of topical PROTACs, exemplified by <b>AH-001</b> and <b>GT20029</b>, androgen receptor degraders, both in clinical trials for androgenetic alopecia, with <b>GT20029</b> also evaluated for acne. We discuss emerging degraders that target clinically relevant proteins, including JAK kinases and BET family members, with applications extending beyond dermatology to pulmonary and ocular diseases and even cosmetic use. Innovative strategies, such as liposomes and microneedle systems, are also enabling effective local delivery. Despite this progress, topical PROTACs face some challenges, such as optimizing the stability, tissue penetration, and selective target engagement under physiological conditions. We conclude by outlining strategic directions that could accelerate the clinical translation of this emerging therapeutic modality.

Journal of Medicinal ChemistryVol. 68(22)
Università degli Studi del Piemonte Orientale “Amedeo Avogadro” (IT), Fondazione IRCCS Istituto Nazionale dei Tumori (IT)
Openalex Percentile: Top 14%
Protein Degradation and Inhibitors
1.61
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