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Phase IIb randomized CONTROL study demonstrates a novel topical isotretinoin formulation, TMB-001, is safe and effective in participants with either recessive X-linked or autosomal recessive lamellar congenital ichthyosis.
Murrell, Dedee F; Teng, Joyce M C; Guenthner, Scott; Marathe, Kalyani; Kempers, Steven; Eads, Kimmie; Castelo-Soccio, Leslie; Mendelsohn, Alan M; Raiz, Jessica; Bunick, Christopher G.
Afiliação
  • Murrell DF; University of New South Wales, School of Medicine, Sydney, NSW, Australia.
  • Teng JMC; School of Medicine, Stanford University, Palo Alto, CA, USA.
  • Guenthner S; The Dermatology Center of Indiana, Plainfield, IN, USA.
  • Marathe K; The Indiana Clinical Trials Center, PC, Plainfield, IN, USA.
  • Kempers S; Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
  • Eads K; Associated Skin Care Specialists, New Brighton, MN, USA.
  • Castelo-Soccio L; The Indiana Clinical Trials Center, PC, Plainfield, IN, USA.
  • Mendelsohn AM; University of Pennsylvania, Perelman School of Medicine and Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Raiz J; Timber Pharmaceuticals, Basking Ridge, NJ, USA.
  • Bunick CG; Timber Pharmaceuticals, Basking Ridge, NJ, USA.
Clin Exp Dermatol ; 48(6): 623-630, 2023 Jun 05.
Article em En | MEDLINE | ID: mdl-36794376
ABSTRACT

BACKGROUND:

In two severe congenital ichthyosis subtypes, autosomal recessive lamellar ichthyosis (ARCI-LI) and X-linked recessive ichthyosis (XLRI), cutaneous manifestations include widespread scaling. Approved topical treatment options are limited to emollients and keratolytics.

AIM:

This analysis from the randomized phase IIb CONTROL study assessed whether the efficacy and safety of TMB-001, a novel topical isotretinoin ointment formulation, differed between ARCI-LI and XLRI subtypes.

METHODS:

Participants ≥ 9 years with genetically confirmed XLRI or ARCI-LI and ≥ 2 (of 4) Visual Index for Ichthyosis Severity (VIIS) assessment areas with ≥ 3 scaling score were randomized 1 1 1 to TMB-001 0.05%/TMB-001 0.1%/vehicle, twice daily for 12 weeks. The proportion of participants with ≥ 50% reduction vs. baseline in VIIS scaling (VIIS 50; primary endpoint) and ≥ 2-grade reduction in Investigator's Global Assessment (IGA)-scaling score vs. baseline (key secondary endpoint) were evaluated. Adverse events (AEs) were monitored.

RESULTS:

Among enrolled participants (TMB-001 0.05%, n = 11; 0.1%, n = 10; and vehicle, n = 12), 52% had ARCI-LI and 48% XLRI subtypes. Mean age was 33.6 and 35.4 years for participants with ARCI-LI and XLRI, respectively. Overall, 33%, 50% and 17% of participants with ARCI-LI and 100%, 33% and 75% of participants with XLRI achieved VIIS 50 in the TMB-001 0.05%, TMB-001 0.1% and vehicle groups, respectively (nominal P = 0.24 for 0.05% vs. vehicle, intent-to-treat population). Improvement of ≥ 2-grade IGA score was observed in 33%, 50% and 0% of participants with ARCI-LI and 83%, 33% and 25% of participants with XLRI in the TMB-001 0.05%, TMB-001 0.1% and vehicle groups, respectively (nominal P = 0.03 for 0.05% vs. vehicle, intention-to-treat population). Most AEs were application-site reactions.

CONCLUSION:

Regardless of congenital ichthyosis subtype, TMB-001 demonstrated greater proportions of participants achieving VIIS 50 and ≥ 2-grade IGA improvement vs. vehicle.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Eritrodermia Ictiosiforme Congênita / Ictiose Ligada ao Cromossomo X / Ictiose Lamelar / Ictiose Tipo de estudo: Clinical_trials Limite: Adult / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Eritrodermia Ictiosiforme Congênita / Ictiose Ligada ao Cromossomo X / Ictiose Lamelar / Ictiose Tipo de estudo: Clinical_trials Limite: Adult / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article