Publication:
Topical Tirbanibulin, a Dual Src Kinase and Tubulin Polymerization Inhibitor, for the Treatment of Plaque-Type Psoriasis: Phase I Results

cris.lastimport.scopus2025-05-07T21:55:30Z
cris.virtual.departmentDermatology-NTUHen_US
cris.virtual.departmentDermatologyen_US
cris.virtual.departmentDermatologyen_US
cris.virtual.departmentDermatology-NTUHen_US
cris.virtual.departmentInternal Medicine-NTUHen_US
cris.virtual.orcid0000-0001-9467-6463en_US
cris.virtual.orcid0000-0002-1498-1474en_US
cris.virtual.orcid0000-0002-5196-7030en_US
cris.virtualsource.department9f25d2c7-1f89-45a3-b730-7a574df8b0e6
cris.virtualsource.department9f25d2c7-1f89-45a3-b730-7a574df8b0e6
cris.virtualsource.departmentb8479706-979d-4714-b78c-cff2dd195c6b
cris.virtualsource.departmentb8479706-979d-4714-b78c-cff2dd195c6b
cris.virtualsource.department4428ecdb-62bd-45e8-bae8-0185d0dee498
cris.virtualsource.orcid9f25d2c7-1f89-45a3-b730-7a574df8b0e6
cris.virtualsource.orcidb8479706-979d-4714-b78c-cff2dd195c6b
cris.virtualsource.orcid4428ecdb-62bd-45e8-bae8-0185d0dee498
dc.contributor.authorJIN-BON HONGen_US
dc.contributor.authorWu, Po-Yuanen_US
dc.contributor.authorQin, Alberten_US
dc.contributor.authorYI-WEN HUANG
dc.contributor.authorTseng, Kuan-Chiaoen_US
dc.contributor.authorLai, Ching-Yuen_US
dc.contributor.authorChan, Wing-Kaien_US
dc.contributor.authorFang, Janeen_US
dc.contributor.authorCutler, David Len_US
dc.contributor.authorTSEN-FANG TSAIen_US
dc.date.accessioned2023-06-27T05:25:24Z
dc.date.available2023-06-27T05:25:24Z
dc.date.issued2022-10-11
dc.description.abstractPlaque-type psoriasis is a common skin disorder. Tirbanibulin (KX01) is a new Src kinase inhibitor with potent antiproliferative activity against keratinocytes and has been approved for treatment of actinic keratosis. This Phase I study investigates the safety and activity of KX01 ointment in patients with plaque-type psoriasis. We recruited 28 patients from two medical centers in Taiwan. This study was performed in four stages. Double-blind treatments were randomized in stages I (KX01 0.01% + placebo, two rounds of two-week treatment) and II (KX01 0.1% + placebo, four weeks) and open-labelled in stages III (KX01 1%, five days) and IV (KX01 1%, five days weekly for four weeks). The safety, tolerability, KX01 concentration, target area score, physician global assessment, and disease relapse were determined. Most treatment-emergent adverse events were mild-to-moderate application site reactions. Three (50.0%) subjects from the stage IV group showed ≥50% reduction in the target area score (TAS50), while two subjects (33.3%) showed a clinically meaningful improvement in the physician global assessment score. KX01 0.01%, 0.1%, and 1% were safe and well-tolerated. KX01 1% at four weeks showed a promising activity for the treatment of plaque-type psoriasis.en_US
dc.identifier.doi10.3390/pharmaceutics14102159
dc.identifier.issn1999-4923
dc.identifier.pmid36297594
dc.identifier.scopus2-s2.0-85140952384
dc.identifier.urihttps://scholars.lib.ntu.edu.tw/handle/123456789/633140
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85140952384
dc.language.isoenen_US
dc.relation.ispartofPharmaceuticsen_US
dc.relation.journalissue10en_US
dc.relation.journalvolume14en_US
dc.subjectKX01en_US
dc.subjectclinical trialen_US
dc.subjectpsoriasisen_US
dc.subjecttirbanibulinen_US
dc.titleTopical Tirbanibulin, a Dual Src Kinase and Tubulin Polymerization Inhibitor, for the Treatment of Plaque-Type Psoriasis: Phase I Resultsen_US
dc.typejournal articleen
dspace.entity.typePublication
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