Maximal use of 0.05% topical isotretinoin in patients with congenital ichthyosis results in low systemic exposure

Congenital ichthyoses (CI) are rare, inherited skin disorders characterized by hyperkeratosis, scaling and fissuring that significantly impair patients' quality of life. Treatment options are limited, with systemic retinoids reserved for severe cases owing to their adverse effect profile. This open-label, single-arm, maximal-use trial investigated the systemic exposure and safety of a topically administered isotretinoin ointment (TMB-001 0.05%) in patients with moderate-to-severe CI. Thirty-four patients aged ≥6 years applied TMB-001 0.05% under maximal-use conditions (twice daily to 75%-90% of the body surface area) for 14 days, with continued application for another 10 weeks. Exposure levels for TMB-001 0.05% and its metabolites were < 1% of those observed after single oral administration of 80 mg isotretinoin to healthy adults. A majority of patients had local safety or tolerability issues, most of which were mild. Overall, the treatment was well tolerated with no evidence of systemic toxicity.

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Publication Details

Journal
British Journal of Clinical Pharmacology
Published
2025-12-17
DOI
https://doi.org/10.1002/bcp.70423
Primary Topic
Skin and Cellular Biology Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Maximal use of 0.05% topical isotretinoin in patients with congenital ichthyosis results in low systemic exposure

J. Stinson, Joyce Teng, Ulrike Blume‐Peytavi, Christopher G. Bunick et al.
British Journal of Clinical Pharmacology
Skin and Cellular Biology Research
article

Maximal use of 0.05% topical isotretinoin in patients with congenital ichthyosis results in low systemic exposure

J. Stinson, Joyce Teng, Ulrike Blume‐Peytavi, Christopher G. Bunick, Holm Schneider, Lara Wine Lee, Thy Huynh, Kathrin Hillmann, Nicolai Peschel, Alan M. Mendelsohn, Steven Kempers
article en

Abstract

Congenital ichthyoses (CI) are rare, inherited skin disorders characterized by hyperkeratosis, scaling and fissuring that significantly impair patients' quality of life. Treatment options are limited, with systemic retinoids reserved for severe cases owing to their adverse effect profile. This open-label, single-arm, maximal-use trial investigated the systemic exposure and safety of a topically administered isotretinoin ointment (TMB-001 0.05%) in patients with moderate-to-severe CI. Thirty-four patients aged ≥6 years applied TMB-001 0.05% under maximal-use conditions (twice daily to 75%-90% of the body surface area) for 14 days, with continued application for another 10 weeks. Exposure levels for TMB-001 0.05% and its metabolites were < 1% of those observed after single oral administration of 80 mg isotretinoin to healthy adults. A majority of patients had local safety or tolerability issues, most of which were mild. Overall, the treatment was well tolerated with no evidence of systemic toxicity.

British Journal of Clinical PharmacologyVol. 92(4)
Medical University of South Carolina (US), Yale University (US), University of Mississippi (US), Universitätsklinikum Erlangen (DE), Associated Skin Care Specialists (US), Leo Pharma (United States) (US), Leo Pharma (Denmark) (DK), Charité - Universitätsmedizin Berlin (DE), Stanford University (US)
LEO Pharma
Openalex Percentile: Top 57%
Skin and Cellular Biology Research
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