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The Palmoplantar Keratoderma therapeutic pipeline features 3+ major pharmaceutical companies actively engaged in developing 3+ innovative treatment approaches for Palmoplantar Keratoderma management, according to DelveInsight's comprehensive analysis.
Palmoplantar keratoderma (PPK) encompasses a collection of dermatological conditions marked by excessive skin thickening on the hands' palms and feet's soles. This condition may be secondary (most prevalent) resulting from medical conditions or environmental exposures, or hereditary caused by genetic alterations affecting keratin, an essential skin structural protein.
Clinical manifestations of PPK include extensive hyperkeratosis across palms and soles, frequently accompanied by erythematous borders around affected areas. Secondary keratotic formations may appear on dorsal surfaces of hands and feet, knee areas, and elbow regions. Additional characteristic features encompass hyperhidrosis and nail dystrophy.
Management approaches typically utilize topical keratolytic agents, including salicylic acid preparations and benzoic acid derivatives, designed to diminish hyperkeratotic tissue.
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DelveInsight's "Palmoplantar Keratoderma Pipeline Analysis 2024" delivers an extensive examination of current clinical research activities and market expansion opportunities within the Palmoplantar Keratoderma treatment sector.
DelveInsight's comprehensive PPK pipeline assessment reveals a dynamic development environment featuring 3+ pharmaceutical companies actively pursuing 3+ therapeutic candidates for Palmoplantar Keratoderma intervention.
Leading PPK pharmaceutical companies including Sol-Gel Technologies Ltd., Krystal Biotech Inc., and additional industry players are investigating novel therapeutic agents for PPK to enhance current treatment options.
Notable PPK pipeline candidates across various developmental phases encompass SGT-210, among other promising compounds.
A Phase 1b clinical investigation assessed KM-001, an innovative TRPV3 antagonist, in PPK patients, encompassing Pachyonychia Congenita (PC) and Punctate Palmoplantar Keratoderma type 1 (PPPK1). Results indicated favorable safety profiles and promising effectiveness, with 86% of Israeli participants and 88% of UK participants demonstrating enhancement in one or more outcome measures, including disease severity, pain levels, or pruritus. Significantly, 47% of all subjects improved across multiple parameters, while six of ten PC patients experienced pain amelioration.
During 2024, Sol-Gel Technologies launched a Phase 1 proof-of-concept investigation for SGT-210, focusing on PPK treatment. This research seeks to evaluate the safety profile and therapeutic potential of this innovative agent, representing a crucial advancement in PPK therapeutic development.
A Phase 2 clinical investigation is actively enrolling participants to assess Tapinarof's safety and effectiveness, a naturally derived compound previously utilized for psoriasis treatment, in adult PPK patients. This research exemplifies efforts to repurpose established dermatological therapies for PPK treatment.
In August 2024, the European Medicines Agency (EMA) awarded orphan drug status to a novel therapeutic compound, designated as (R)-(3-(2'-cyclopropyl-3-(hydroxymethyl)-[1,1'-biphenyl]-4-yl)pyrrolidin-1-yl)(5-fluoropyridin-2-yl)methanone, for punctate palmoplantar keratoderma treatment. This designation supports therapeutic development for rare conditions such as PPK.
The analysis encompasses:
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SGT-210: Sol-Gel Technologies Ltd.
Approximately three or more pharmaceutical companies are currently developing PPK therapies. Sol-Gel Technologies Ltd. maintains the most advanced therapeutic candidate, currently undergoing Phase I clinical evaluation.
DelveInsight's analysis encompasses 3+ therapeutic products across multiple clinical developmental stages:
Therapeutic products are classified under various administration methods:
Therapeutic candidates are categorized by molecular structure:
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