Also known as: Protein Transduction Domain - Dvl Binding Motif, CXXC5 / Dvl Inhibitor
Half-life: Variable; topical residence-time dependent
Last reviewed: · Published:
PTD-DBM is a synthetic peptide consisting of a protein transduction domain (PTD, a short cationic peptide that allows passage across cell membranes) fused to the Dvl-binding motif (DBM) of the CXXC5 protein. CXXC5 is a negative-feedback inhibitor of Wnt/β-catenin signaling in hair follicles that becomes upregulated during the catagen phase and contributes to hair-cycle slowdown. By introducing the CXXC5-mimetic DBM peptide into follicle cells (via the PTD-driven membrane crossing), PTD-DBM competitively displaces CXXC5 from Dishevelled (Dvl), restoring Wnt signaling and reactivating the anagen growth phase.
Preclinical work from Kang-Yell Choi's group at Yonsei University in South Korea — the same lab that originally characterized CXXC5's role in hair-cycle regulation — has shown that topical PTD-DBM in combination with valproic acid (another Wnt-pathway activator) produced substantial hair regrowth in mouse models. A Phase 1/2 clinical trial of a related Wnt-pathway combination has been conducted, though regulatory approval has not been achieved.
PTD-DBM is a topical investigational ingredient with a novel and well-characterized mechanism. Research-chemical vendors sell the peptide for cosmetic formulators interested in hair-loss applications. Clinical efficacy in human androgenetic alopecia outside of investigator-sponsored research is not established.
CXXC5 was identified as a negative regulator of Wnt-induced hair cycling by Kang-Yell Choi's group at Yonsei University in research published from 2014 onward. The PTD-DBM peptide therapeutic concept emerged from that same line of work, with the peptide being designed specifically to disrupt the CXXC5-Dvl interaction in hair follicles. The technology was spun out as the basis of a clinical development program by the Korean biotech CK Regeon.
Animal tolerability has been good in published mouse studies. Limited human safety data is available from early-stage trials. Because Wnt/β-catenin signaling is broadly relevant to cell proliferation, chronic systemic activation has theoretical concerns including the risk of stimulating dysplastic or neoplastic cells. Topical application limits systemic exposure but does not eliminate it entirely.
Dose Range
Variable per formulation
Frequency
Daily topical application to scalp
Duration
12-24 weeks minimum for visible results
Dosing information is for educational purposes only. Consult a healthcare professional before using any peptide.
Typical Vial Size
5 mg
Water Type
Not typically reconstituted as injectable — formulated as topical
Mixing Volume
N/A mL
Half-Life
Variable; topical residence-time dependent
Molecular Weight
~2,500 Da
PTD-DBM is incorporated into topical hair-loss formulations, often with co-actives like valproic acid. Not intended for injection. Store dry powder cool and dry.
FDA Status
Not FDA approved.
Legal Status
Unregulated research / cosmetic ingredient depending on formulation.
USA
Not approvedResearch-only
EU
Not approvedNot authorized as medicinal product
UK
Not approvedClassified as research chemical
South Korea
Not approvedClinical development program ongoing at CK Regeon
Australia
Not approvedTGA has not evaluated
Canada
Not approvedNot authorized for human use
Kim HY, Yoon JY, Yun JH, Cho KW, Lee SH, Rhee YM, Jung HS, Lim HJ, Lee H, Choi J, Heo JN, Lee W, No KT, Min D, Choi KY
Cell Death & Differentiation (2015)
Foundational identification of CXXC5 as a negative-feedback inhibitor of Wnt/β-catenin signaling, providing the molecular target for the PTD-DBM peptide therapeutic strategy.
View Study →Lee SH, Seo SH, Lee DH, Pi LQ, Lee WS, Choi KY
Journal of Investigative Dermatology (2016)
Demonstrated that disrupting the CXXC5-Dvl interaction (the strategy used by PTD-DBM peptide) produced hair regrowth in mouse models, validating the mechanism for therapeutic hair-loss application.
View Study →Ryu YC, Lee DH, Shim J, Park J, Kim YR, Choi S, Bak SS, Sung YK, Lee SH, Choi KY
Journal of Investigative Dermatology (2019)
Specific demonstration of PTD-DBM peptide efficacy combined with valproic acid in promoting hair regrowth in mice with an androgenetic alopecia-like phenotype, supporting clinical translation.
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