222. 一次性ネフローゼ症候群 Primary nephrotic syndrome Clinical trials / Disease details
臨床試験数 : 310 / 薬物数 : 295 - (DrugBank : 117) / 標的遺伝子数 : 63 - 標的パスウェイ数 : 194
| 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 | EUCTR2020-000384-23-DE (EUCTR) | 19/12/2022 | 17/05/2022 | A study to test BI 764198 in people with a type of kidney disease calledfocal segmental glomerulosclerosis. | A multicenter, randomized, double-blind, parallel group, placebo controlled study to assess the efficacy, safety, tolerability, pharmacokinetics and pharmacodynamics profile of BI 764198 administered orally once daily for 12 weeks in patients with focal segmental glomerulosclerosis - PoCP study in FSGS | Focal segmental glomerulosclerosis MedDRA version: 21.1;Level: PT;Classification code 10067757;Term: Focal segmental glomerulosclerosis;System Organ Class: 10038359 - Renal and urinary disorders;Therapeutic area: Diseases [C] - Injuries, poisonings, and occupational diseases [C21] | Product Code: BI 764198 INN or Proposed INN: None yet Other descriptive name: BI 764198 Product Code: BI 764198 INN or Proposed INN: None yet Other descriptive name: BI 764198 Product Code: BI 764198 INN or Proposed INN: None yet Other descriptive name: BI 764198 | Boehringer Ingelheim Pharma GmbH & Co. KG | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 60 | Phase 2 | France;United States;Hungary;Belgium;Spain;Ireland;Australia;Germany;United Kingdom;Italy;China | ||
| 2 | EUCTR2020-000384-23-ES (EUCTR) | 17/05/2022 | 28/03/2022 | A study to test BI 764198 in people with a type of kidney disease called focal segmental glomerulosclerosis (FSGS). | A multicenter, randomized, double-blind, parallel group, placebo controlled study to assess safety, tolerability, pharmacokinetics and pharmacodynamics of BI 764198 administered orally once daily for 12 weeks in patients with focal segmental glomerulosclerosis - PoCP study in FSGS | Glomerulosclerosis MedDRA version: 21.1;Level: PT;Classification code 10067757;Term: Focal segmental glomerulosclerosis;System Organ Class: 10038359 - Renal and urinary disorders;Therapeutic area: Diseases [C] - Injuries, poisonings, and occupational diseases [C21] | Product Code: BI 764198 INN or Proposed INN: None yet Other descriptive name: BI 764198 Product Code: BI 764198 INN or Proposed INN: None yet Other descriptive name: BI 764198 Product Code: BI 764198 INN or Proposed INN: None yet Other descriptive name: BI 764198 | Boehringer Ingelheim España S.A. | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 60 | Phase 2 | United States;Hungary;Belgium;France;Spain;Ireland;Australia;Germany;United Kingdom;Italy | ||
| 3 | NCT05213624 (ClinicalTrials.gov) | March 10, 2022 | 27/1/2022 | A Study to Test BI 764198 in People With a Type of Kidney Disease Called Primary Focal Segmental Glomerulosclerosis | A Multicenter, Randomized, Double-blind, Parallel Group, Placebo Controlled Study to Assess the Efficacy, Safety, Tolerability, Pharmacokinetics and Pharmacodynamics Profile of BI 764198 Administered Orally Once Daily for 12 Weeks in Patients With Focal Segmental Glomerulosclerosis | Kidney Disease, Chronic | Drug: BI 764198;Drug: Placebo | Boehringer Ingelheim | NULL | Recruiting | 18 Years | 75 Years | All | 60 | Phase 2 | United States;Australia;Belgium;China;France;Germany;Ireland;Italy;New Zealand;Spain;United Kingdom |