160. 先天性魚鱗癬 Congenital ichthyosis Clinical trials / Disease details
臨床試験数 : 42 / 薬物数 : 71 - (DrugBank : 21) / 標的遺伝子数 : 18 - 標的パスウェイ数 : 112
Showing 1 to 10 of 42 diseases
No. | TrialID | Date_ enrollment | Date_ registration | Public_title | Scientific_title | Condition | Intervention | Primary_ sponsor | Secondary_ sponsor | Recruitment_ Status | Inclusion_ agemin | Inclusion_ agemax | Inclusion_ gender | Target_ size | Phase | Countries |
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1 | NCT05735158 (ClinicalTrials.gov) | March 2023 | 9/2/2023 | Topical KB105 for the Treatment of TGM1-deficient Autosomal Recessive Congenital Ichthyosis (ARCI) | A Phase 2, Randomized, Placebo-controlled Study of Topical KB105, a Replication-defective, Non-integrating HSV-1 Vector Expressing Human Transglutaminase 1 (TGM1) for the Treatment of TGM1-deficient Autosomal Recessive Congenital Ichthyosis (ARCI) A Phase 2, Randomized, Placebo-controlled Study of Topical KB105, a Replication-defective, Non-integ ... | Autosomal Recessive Ichthyosis | Biological: KB105;Other: Placebo | Krystal Biotech, Inc. | NULL | Not yet recruiting | 6 Months | N/A | All | 15 | Phase 2 | United States |
2 | NCT05443685 (ClinicalTrials.gov) | January 2, 2023 | 10/6/2022 | ADX-629 Therapy for Sjogren-Larsson Syndrome | An Open-Label, Phase 1/2, Single-Site Study of the Safety, Biochemical Efficacy, and Exploratory Clinical Effects of Oral ADX-629 in Subjects With Sjögren-Larsson Syndrome An Open-Label, Phase 1/2, Single-Site Study of the Safety, Biochemical Efficacy, and Exploratory Cli ... | Sjogren-Larsson Syndrome | Drug: ADX-629 | William Rizzo, MD | NULL | Recruiting | 18 Years | 50 Years | All | 10 | Phase 1/Phase 2 | United States |
3 | NCT05583669 (ClinicalTrials.gov) | November 8, 2022 | 13/10/2022 | A Study to Assess the Safety and Pharmacokinetics of Multiple Ascending Subcutaneous Doses of DS-2325a in Healthy Subjects A Study to Assess the Safety and Pharmacokinetics of Multiple Ascending Subcutaneous Doses of DS-232 ... | A Phase 1, Subject- and Investigator-Blinded, Sponsor-Unblinded, Placebo-Controlled, Randomized, Sequential Cohort Study to Assess the Safety and Pharmacokinetics of Multiple Ascending Subcutaneous Doses of DS-2325a in Healthy Subjects A Phase 1, Subject- and Investigator-Blinded, Sponsor-Unblinded, Placebo-Controlled, Randomized, Seq ... | Netherton Syndrome | Drug: DS-2325a;Drug: Placebo | Daiichi Sankyo, Inc. | NULL | Recruiting | 18 Years | 50 Years | All | 24 | Phase 1 | United States |
4 | NCT05388903 (ClinicalTrials.gov) | June 20, 2022 | 19/5/2022 | A Study to Assess the Safety and Pharmacokinetics of Single Ascending Subcutaneous and Intravenous Doses of DS-2325a in Healthy Subjects A Study to Assess the Safety and Pharmacokinetics of Single Ascending Subcutaneous and Intravenous D ... | A Phase 1, Subjects- and Investigator-Blinded, Sponsor-Unblinded, Placebo-Controlled, Randomized, Sequential Cohort Study to Assess the Safety and Pharmacokinetics of Single Ascending Subcutaneous and Intravenous Doses of DS-2325a in Healthy Subjects A Phase 1, Subjects- and Investigator-Blinded, Sponsor-Unblinded, Placebo-Controlled, Randomized, Se ... | Netherton Syndrome | Drug: DS-2325a;Drug: Placebo | Daiichi Sankyo, Inc. | NULL | Completed | 18 Years | 45 Years | All | 64 | Phase 1 | United States |
5 | ChiCTR2200059272 | 2022-06-01 | 2022-04-27 | A Basket Trial of the Safety and Efficacy of Ixekizumab in Participants with Autoimmune Inflammatory Skin Diseases A Basket Trial of the Safety and Efficacy of Ixekizumab in Participants with Autoimmune Inflammatory ... | A Basket Trial of the Safety and Efficacy of Ixekizumab in Participants with Autoimmune Inflammatory Skin Diseases A Basket Trial of the Safety and Efficacy of Ixekizumab in Participants with Autoimmune Inflammatory ... | pityriasis rubra pilaris, hidradenitis suppurativa, Netherton syndrome, erythrokeratodermia variabilis and erythrokeratoderma progressive symmetrica pityriasis rubra pilaris, hidradenitis suppurativa, Netherton syndrome, erythrokeratodermia variabil ... | pityriasis rubra pilaris, Netherton syndrome, erythrokeratodermia variabilis and erythrokeratoderma progressive symmetrica:Ixekizumab at different doses in adults and juveniles with different body weight;hidradenitis suppurativa:Ixekizumab at different doses in adults and juveniles with different body weight; pityriasis rubra pilaris, Netherton syndrome, erythrokeratodermia variabilis and erythrokeratoderma ... | Dermatology Hospital of Southern Medical University | NULL | Pending | Both | pityriasis rubra pilaris, Netherton syndrome, erythrokeratodermia variabilis and erythrokeratoderma progressive symmetrica:30;hidradenitis suppurativa:10; | Phase 2 | China | ||
6 | EUCTR2021-003210-39-AT (EUCTR) | 01/02/2022 | 08/09/2021 | A phase I/II, multicenter, randomized, double-blind, placebo within-patient controlled study to evaluate the safety and efficacy SXR1096 skin cream in patients with Netherton syndrome (NS) A phase I/II, multicenter, randomized, double-blind, placebo within-patient controlled study to eval ... | A phase I/II, multicenter, randomized, double-blind, placebo within-patient controlled, first-time-in-man (FTIM) Proof of Concept (PoC) study to evaluate the safety and efficacy of topically applied SXR1096 skin cream in patients with Netherton syndrome (NS) A phase I/II, multicenter, randomized, double-blind, placebo within-patient controlled, first-time-i ... | Netherton syndrome MedDRA version: 20.0;Level: PT;Classification code 10062909;Term: Netherton's syndrome;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Skin and Connective Tissue Diseases [C17] Netherton syndrome MedDRA version: 20.0;Level: PT;Classification code 10062909;Term: Netherton's syn ... | Product Code: SXR1096 INN or Proposed INN: SXR1096 Other descriptive name: SXR1096 | Sixera Pharma | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 20 | Phase 1;Phase 2 | Finland;Austria | ||
7 | EUCTR2021-003210-39-FI (EUCTR) | 23/11/2021 | 20/08/2021 | A phase I/II, multicenter, randomized, double-blind, placebo within-patient controlled study to evaluate the safety and efficacy of SXR1096 skin cream in patients with Netherton syndrome (NS) A phase I/II, multicenter, randomized, double-blind, placebo within-patient controlled study to eval ... | A phase I/II, multicenter, randomized, double-blind, placebo within-patient controlled, first-time-in-man (FTIM) Proof of Concept (PoC) study to evaluate the safety and efficacy of topically applied SXR1096 skin cream in patients with Netherton syndrome (NS) A phase I/II, multicenter, randomized, double-blind, placebo within-patient controlled, first-time-i ... | Netherton-syndrome MedDRA version: 20.0;Level: PT;Classification code 10062909;Term: Netherton's syndrome;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Skin and Connective Tissue Diseases [C17] Netherton-syndrome MedDRA version: 20.0;Level: PT;Classification code 10062909;Term: Netherton's syn ... | Product Code: SXR1096 | Sixera Pharma | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 20 | Phase 1;Phase 2 | Finland | ||
8 | NCT04996485 (ClinicalTrials.gov) | March 1, 2021 | 21/7/2021 | Scientific Substantiation and Assessment of the Effectiveness of Pathogenetic Methods of Therapy for Congenital Ichthyosis in Children Scientific Substantiation and Assessment of the Effectiveness of Pathogenetic Methods of Therapy for ... | Scientific Substantiation and Assessment of the Effectiveness of Pathogenetic Methods of Therapy for Congenital Ichthyosis in Children Scientific Substantiation and Assessment of the Effectiveness of Pathogenetic Methods of Therapy for ... | Congenital Ichthyosis | Drug: Secukinumab Injection;Drug: Ustekinumab Injection;Drug: Dupilumab Injection;Other: Symptomatic therapy Drug: SecukinumabInjection;Drug: UstekinumabInjection;Drug: DupilumabInjection;Other: Symptomatic th ... | National Medical Research Center for Children's Health, Russian Federation | NULL | Recruiting | 6 Months | 18 Years | All | 50 | Phase 4 | Russian Federation |
9 | ChiCTR2000037278 | 2020-09-01 | 2020-08-27 | Effects and Safety of Simvastatin Ointment in the Treatment of Congenital Ichthyosis | Effects and Safety of Simvastatin Ointment in the Treatment of Congenital Ichthyosis | inherited ichthyosis | ARCI group:Concentration of simvastatin cream;XLI group:Concentration of simvastatin cream; | Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine | NULL | Recruiting | Both | ARCI group:45;XLI group:10; | China | |||
10 | NCT04244006 (ClinicalTrials.gov) | July 23, 2020 | 13/1/2020 | A Pilot Study of the Efficacy and Safety of Dupilumab Versus Placebo in Patients With Netherton Syndrome A Pilot Study of the Efficacy and Safety of Dupilumab Versus Placebo in Patients With Netherton Synd ... | A Randomized Double-blinded Pilot Study of the Efficacy and Safety of Dupilumab Versus Placebo in Patients With Netherton Syndrome A Randomized Double-blinded Pilot Study of the Efficacy and Safety of Dupilumab Versus Placebo in Pa ... | Netherton Syndrome | Drug: Dupilumab Prefilled Syringe;Other: Placebo Prefilled Syringe | University Hospital, Toulouse | MedSharing | Recruiting | 18 Years | N/A | All | 24 | Phase 2/Phase 3 | France |