JR-141 ( DrugBank: - )
1 disease
| 告示番号 | 疾患名（ページ内リンク） | 臨床試験数 |
|---|---|---|
| 19 | ライソゾーム病 | 10 |
19. ライソゾーム病
臨床試験数 : 899 / 薬物数 : 684 - (DrugBank : 99) / 標的遺伝子数 : 51 - 標的パスウェイ数 : 182
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1 | NCT05594992 (ClinicalTrials.gov) | February 22, 2023 | 6/10/2022 | An Extension Study of JR-141 to Evaluate the Long-term Safety and Efficacy in Mucopolysaccharidosis Type II (Hunter Syndrome) Male Subjects | An Extension Study of JR-141 to Evaluate the Long-term Safety and Efficacy in Mucopolysaccharidosis Type II (Hunter Syndrome) Male Subjects | Mucopolysaccharidosis II | Drug: JR-141 | JCR Pharmaceuticals Co., Ltd. | NULL | Enrolling by invitation | N/A | N/A | Male | 80 | Phase 3 | United States |
| 2 | EUCTR2020-003200-14-DE (EUCTR) | 16/05/2022 | 15/06/2021 | A Phase III study of JR-141 in Hunter Syndrome patients | A Phase III study of JR-141 in Mucopolysaccharidosis type II (Hunter Syndrome) patients. | Mucopolysaccharidosis type II MedDRA version: 20.1;Level: PT;Classification code 10056889;Term: Mucopolysaccharidosis II;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] | Product Name: Pabinafusp alfa Product Code: JR-141 INN or Proposed INN: Pabinafusp alfa Other descriptive name: JR-141 | JCR Pharmaceuticals Co., Ltd. | NULL | Authorised-recruitment may be ongoing or finished | Female: no Male: yes | 50 | Phase 3 | France;United States;Brazil;Germany;United Kingdom | ||
| 3 | EUCTR2020-003200-14-FR (EUCTR) | 04/05/2022 | 17/06/2021 | A Phase III study of JR-141 in Hunter Syndrome patients | A Phase III study of JR-141 in Mucopolysaccharidosis type II (Hunter Syndrome) patients. | Mucopolysaccharidosis type II MedDRA version: 20.1;Level: PT;Classification code 10056889;Term: Mucopolysaccharidosis II;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] | Product Name: Pabinafusp alfa Product Code: JR-141 INN or Proposed INN: Pabinafusp alfa Other descriptive name: JR-141 | JCR Pharmaceuticals Co., Ltd. | NULL | Authorised-recruitment may be ongoing or finished | Female: no Male: yes | 50 | Phase 3 | United States;France;Brazil;Germany;United Kingdom | ||
| 4 | NCT04573023 (ClinicalTrials.gov) | February 14, 2022 | 17/9/2020 | A Phase III Study of JR-141 in Patients With Mucopolysaccharidosis II | A Phase III Study of JR-141 in Patients With Mucopolysaccharidosis II | Mucopolysaccharidosis II | Drug: JR-141;Drug: Idursulfase;Drug: JR-141 or Idursulfase | JCR Pharmaceuticals Co., Ltd. | NULL | Recruiting | N/A | N/A | Male | 80 | Phase 3 | United States;Brazil;France;Germany;Spain |
| 5 | JPRN-jRCT2031210126 | 27/07/2021 | 31/05/2021 | Post-marketing Clinical Study of IZCARGO in Patients with Mucopolysaccharidosis Type II | Post-marketing Clinical Study of IZCARGO in Patients with Mucopolysaccharidosis Type II | mucopolysaccharidosis type II (MPS II) | [Post-marketing clinical study drug] Name - Post-marketing clinical study drug (code): IZCARGO for I.V. infusion 10 mg (test drug code: JR-141) - Nonproprietary name International nonproprietary name (INN): pabinafusp alfa (r-INN List 82, WHO Drug Information, Vol. 33. No. 3, 2019) Japanese accepted names for pharmaceuticals (JAN) Registered number: 301-4-B3 Japanese name: pabinafusp alfa (genetical recombination) English name: Pabinafusp Alfa (Genetical Recombination) Dose and regimen: Subjects will receive 2.0 mg of pabinafusp alfa (genetical recombination) per kilogram of body weight once a week as an intravenous infusion. | Yamamoto Tatsuyoshi | NULL | Recruiting | Not applicable | Not applicable | Both | 20 | Phase 4 | Japan |
| 6 | NCT04348136 (ClinicalTrials.gov) | September 1, 2019 | 18/12/2019 | An Extension Study of JR-141 in Patients With Mucopolysaccharidosis Type II | An Extension Study of JR-141 in Patients With Mucopolysaccharidosis Type II | Mucopolysaccharidosis II | Drug: JR-141 | JCR Pharmaceuticals Co., Ltd. | NULL | Active, not recruiting | N/A | N/A | Male | 27 | Phase 2/Phase 3 | Japan |
| 7 | NCT03708965 (ClinicalTrials.gov) | January 1, 2019 | 27/9/2018 | An Extension Study of JR-141-BR21 in Patients With Mucopolysaccharidosis II | An Extension Study of JR-141-BR21 in Patients With Mucopolysaccharidosis II | Mucopolysaccharidosis II | Drug: JR-141 | JCR Pharmaceuticals Co., Ltd. | NULL | Active, not recruiting | 0 Years | N/A | Male | 19 | Phase 2 | Brazil |
| 8 | NCT03568175 (ClinicalTrials.gov) | August 1, 2018 | 1/6/2018 | A Study of JR-141 in Patients With Mucopolysaccharidosis II | A Phase II/III Study of JR-141 in Patients With Mucopolysaccharidosis II | Mucopolysaccharidosis II | Drug: JR-141 | JCR Pharmaceuticals Co., Ltd. | NULL | Completed | N/A | N/A | Male | 28 | Phase 2/Phase 3 | Japan |
| 9 | NCT03359213 (ClinicalTrials.gov) | July 26, 2018 | 17/11/2017 | A Study of JR-141 in Patients With Mucopolysaccharidosis II | Phase II Study of JR-141 in Patients With Mucopolysaccharidosis II | Mucopolysaccharidosis II | Drug: JR-141 | JCR Pharmaceuticals Co., Ltd. | NULL | Completed | 0 Years | N/A | Male | 18 | Phase 2 | Brazil |
| 10 | NCT03128593 (ClinicalTrials.gov) | March 30, 2017 | 10/4/2017 | A Study of JR-141 in Patients With Mucopolysaccharidosis Type II | A Phase I/II Study of JR-141 in Patients With Mucopolysaccharidosis Type II | Mucopolysaccharidosis II | Drug: JR-141 | JCR Pharmaceuticals Co., Ltd. | NULL | Completed | 6 Years | N/A | Male | 14 | Phase 1/Phase 2 | Japan |