50. Dermatomyositis Clinical trials / Disease details
Clinical trials : 194 / Drugs : 244 - (DrugBank : 89) / Drug target genes : 50 - Drug target pathways : 151
Showing 1 to 10 of 194 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 | NCT05669014 (ClinicalTrials.gov) | April 2023 | 20/12/2022 | A Phase 2 Proof of Concept Study to Evaluate the Efficacy and Safety of Daxdilimab in Participants With Dermatomyositis (DM) or Anti-synthetase Inflammatory Myositis (ASIM) A Phase 2 Proof of Concept Study to Evaluate the Efficacy and Safety of Daxdilimab in Participants W ... | A Phase 2, Randomized, Double-blind, Placebo-controlled, Efficacy and Safety Study of Daxdilimab Subcutaneous Injection in Adult Participants With Inadequately Controlled Dermatomyositis or Anti-synthetase Inflammatory Myositis. A Phase 2, Randomized, Double-blind, Placebo-controlled, Efficacy and Safety Study of Daxdilimab Sub ... | Idiopathic Inflammatory Myositis | Drug: Daxdilimab;Drug: Placebo | Horizon Therapeutics Ireland DAC | NULL | Not yet recruiting | 18 Years | 75 Years | All | 96 | Phase 2 | NULL |
2 | NCT05695950 (ClinicalTrials.gov) | February 27, 2023 | 13/1/2023 | A Study Evaluating the Effects of GLPG3667 Given as Oral Treatment for up to 24 Weeks in Adults With Dermatomyositis A Study Evaluating the Effects of GLPG3667 Given as Oral Treatment for up to 24 Weeks in Adults With ... | A Randomized, Double-blind, Placebo-controlled, Multi-center Study to Evaluate the Efficacy, Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Orally Administered GLPG3667 Once Daily for 24 Weeks in Adult Subjects With Dermatomyositis A Randomized, Double-blind, Placebo-controlled, Multi-center Study to Evaluate the Efficacy, Safety, ... | Dermatomyositis | Drug: GLPG3667;Drug: Placebo | Galapagos NV | NULL | Recruiting | 18 Years | 75 Years | All | 62 | Phase 2 | United States |
3 | EUCTR2018-003171-35-HU (EUCTR) | 13/02/2023 | 14/12/2022 | A study to evaluate the efficacy, safety, and pharmacokinetics of IgPro20 in adults with dermatomyositis (DM) A study to evaluate the efficacy, safety, and pharmacokinetics of IgPro20 in adults with dermatomyos ... | A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of IgPro20 (Subcutaneous Immunoglobulin, Hizentra®) in Adults with Dermatomyositis (DM) – The RECLAIIM Study A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of IgPro20 (Subcutaneous Immunoglobul ... | Dermatomyositis MedDRA version: 20.0;Level: LLT;Classification code 10001403;Term: Adult dermatomyositis;System Organ Class: 100000004858;Therapeutic area: Diseases [C] - Skin and Connective Tissue Diseases [C17] Dermatomyositis MedDRA version: 20.0;Level: LLT;Classification code 10001403;Term: Adult dermatomyos ... | Trade Name: Hizentra Product Name: human immunoglobulin G Product Code: IgPro20 INN or Proposed INN: human immunoglobulin G Other descriptive name: Hizentra Trade Name: Hizentra Product Name: human immunoglobulin G Product Code: IgPro20 INN or Proposed INN: hu ... | CSL Behring LLC | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 126 | Phase 3 | Argentina;Russian Federation;Hungary;United States;Japan;Ukraine;United Kingdom;Switzerland;Spain;Belgium;European Union;Mexico;Italy;Australia;France;Germany Argentina;Russian Federation;Hungary;United States;Japan;Ukraine;United Kingdom;Switzerland;Spain;Be ... | ||
4 | NCT05650567 (ClinicalTrials.gov) | January 19, 2023 | 6/12/2022 | Study of M5049 in DM and PM Participants (NEPTUNIA) | A Phase IIa, Randomized, Parallel, Double-Blind, Placebo Controlled Study to Evaluate the Efficacy and Safety of Enpatoran in Dermatomyositis and Polymyositis Participants Receiving Standard of Care (NEPTUNIA) A Phase IIa, Randomized, Parallel, Double-Blind, Placebo Controlled Study to Evaluate the Efficacy a ... | Dermatomyositis;Polymyositis | Drug: M5049 high dose;Drug: Placebo | EMD Serono Research & Development Institute, Inc. | Merck KGaA, Darmstadt, Germany | Recruiting | 18 Years | 75 Years | All | 40 | Phase 2 | United States;Germany |
5 | NCT05495321 (ClinicalTrials.gov) | December 1, 2022 | 17/11/2021 | Interleukin-2 on Active Dermatomyositis | Therapeutic Effect of Interleukin-2 on Active Dermatomyositis: A Multicenter, Randomised, Double-blind, Placebo-controlled Trial Therapeutic Effect of Interleukin-2 on Active Dermatomyositis: A Multicenter, Randomised, Double-bli ... | Dermatomyositis | Drug: Interleukin-2 | Peking University People's Hospital | NULL | Enrolling by invitation | 18 Years | 75 Years | All | 240 | Phase 3 | China |
6 | NCT05524311 (ClinicalTrials.gov) | November 10, 2022 | 5/7/2022 | Baricitinib in the Treatment of New-onset Juvenile Dermatomyositis (MYOCIT) | Baricitinib in the Treatment of New-onset Juvenile Dermatomyositis | Juvenile Dermatomyositis | Drug: Baricitinib;Biological: pharmacokinetics study;Biological: dosage of cytokines;Biological: transcriptomic analysis;Behavioral: Parent version of the Child Health Questionnaire (CHQ);Behavioral: Childhood Health Assessment Questionnaire;Biological: Pregnancy test Drug: Baricitinib;Biological: pharmacokinetics study;Biological: dosage of cytokines;Biological: tra ... | Assistance Publique - Hôpitaux de Paris | NULL | Recruiting | 3 Years | 18 Years | All | 16 | Phase 2 | France |
7 | NCT05437263 (ClinicalTrials.gov) | October 31, 2022 | 24/6/2022 | A Study to Investigate the Efficacy and Safety of Brepocitinib in Adults With Dermatomyositis | A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Investigate the Efficacy and Safety of Oral Brepocitinib in Adults With Dermatomyositis A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Investigate the Efficacy and Safety ... | Dermatomyositis | Drug: Brepocitinib;Drug: Placebo | Priovant Therapeutics, Inc. | NULL | Recruiting | 18 Years | 75 Years | All | 225 | Phase 3 | United States;Bulgaria;Czechia;Germany;Hungary;Israel;Italy;Poland;Romania;Slovakia;Spain |
8 | NCT04972760 (ClinicalTrials.gov) | August 31, 2022 | 14/6/2021 | Baricitinib in Patients With Relapsing or naïve Dermatomyositis | Baricitinib in Patients With Relapsing or naïve Dermatomyositis: a Multicenter Randomized Controlled Trial (BIRD) Baricitinib in Patients With Relapsing or naïve Dermatomyositis: a Multicenter Randomized Controlled ... | Dermatomyositis | Drug: Baricitinib;Drug: Placebo | Assistance Publique - Hôpitaux de Paris | NULL | Recruiting | 18 Years | 74 Years | All | 62 | Phase 3 | France |
9 | EUCTR2021-004787-10-ES (EUCTR) | 04/05/2022 | 08/02/2022 | An Extension Study for Participants Who Have Completed the Treatment Period of a Qualifying Parent Study An Extension Study for Participants Who Have Completed the Treatment Period of a Qualifying Parent S ... | AN OPEN LABEL, LONG-TERM EXTENSION STUDY TO INVESTIGATE THE SAFETY OF PF-06823859 ADMINISTERED TO ADULT PARTICIPANTS =18 AND =80 WITH ACTIVE DERMATOMYOSITIS. AN OPEN LABEL, LONG-TERM EXTENSION STUDY TO INVESTIGATE THE SAFETY OF PF-06823859 ADMINISTERED TO AD ... | Dermatomyositis MedDRA version: 20.0;Level: PT;Classification code 10012503;Term: Dermatomyositis;System Organ Class: 10040785 - Skin and subcutaneous tissue disorders;Therapeutic area: Diseases [C] - Immune System Diseases [C20] Dermatomyositis MedDRA version: 20.0;Level: PT;Classification code 10012503;Term: Dermatomyositis;Sy ... | Product Name: PF-06823859 Product Code: PF-06823859 INN or Proposed INN: PF-06823859 Other descriptive name: Humanised IgG1K monoclonal antibody against interferon beta Product Name: PF-06823859 Product Code: PF-06823859 INN or Proposed INN: PF-06823859 Other descriptive ... | Pfizer Inc. | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 20 | Phase 2 | United States;Hungary;Poland;Spain;Australia;Germany;Italy | ||
10 | NCT05361109 (ClinicalTrials.gov) | May 1, 2022 | 3/4/2022 | Baricitinib for Cutaneous Dermatomyositis | An Open-Label Pilot Study to Evaluate the Efficacy and Safety of Baricitinib in Subjects With Cutaneous Dermatomyositis An Open-Label Pilot Study to Evaluate the Efficacy and Safety of Baricitinib in Subjects With Cutane ... | Dermatomyositis | Drug: Baricitinib | University of Washington | NULL | Not yet recruiting | 18 Years | N/A | All | 10 | Phase 2 | United States |