GSK2315698 ( DrugBank: - )


1 disease
告示番号疾患名(ページ内リンク)臨床試験数
28全身性アミロイドーシス3

28. 全身性アミロイドーシス


臨床試験数 : 267 薬物数 : 241 - (DrugBank : 77) / 標的遺伝子数 : 68 - 標的パスウェイ数 : 180
No.TrialIDDate_
enrollment
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registration
Public_titleScientific_titleConditionInterventionPrimary_
sponsor
Secondary_
sponsor
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Inclusion_
agemin
Inclusion_
agemax
Inclusion_
gender
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size
PhaseCountries
1EUCTR2016-000276-23-GB
(EUCTR)
06/12/201611/07/2016Study to look at the affect of anti-SAP treatment in patients with cardiac amyloidosis A multiple treatment session, open label phase 2 clinical study of GSK2398852 administered following and together with GSK2315698 in cohorts of patients with cardiac amyloidosis Systemic amyloidosis
MedDRA version: 20.0;Level: SOC;Classification code 10021428;Term: Immune system disorders;System Organ Class: 10021428 - Immune system disorders
MedDRA version: 20.0;Level: PT;Classification code 10002022;Term: Amyloidosis;System Organ Class: 10021428 - Immune system disorders ;Therapeutic area: Diseases [C] - Nervous System Diseases [C10]
Product Name: GSK2315698
Product Code: GSK2315698
INN or Proposed INN: miridesap
Other descriptive name: CPHC (carboxy pyrrolidine hexanoyl pyrrolidone carboxylate)
Product Name: GSK2398852
Product Code: GSK2398852
INN or Proposed INN: dezamizumab
GlaxoSmithKline Research & Development LtdNULLNot Recruiting Female: yes
Male: yes
30 Human pharmacology (Phase 1): no Therapeutic exploratory (Phase 2): yes Therapeutic confirmatory - (Phase 3): no Therapeutic use (Phase 4): noUnited States;United Kingdom
2NCT01777243
(ClinicalTrials.gov)
May 13, 201324/1/2013A Study to Evaluate the Safety of GSK2398852 When Co-administered With GSK2315698 in Patients With Systemic AmyloidosisA Single Dose First in Human Study of GSK2398852 Co-Administered With GSK2315698 in Patients With Systemic AmyloidosisAmyloidosisDrug: GSK2398852;Drug: GSK2315698GlaxoSmithKlineImperial College London;Heart Hospital;Royal Free Hospital NHS Foundation Trust;Quintiles, Inc.Completed18 Years70 YearsAll25Phase 1United Kingdom
3NCT01406314
(ClinicalTrials.gov)
October 13, 201126/7/2011SAP Depleter Dose Assessment Study in PatientsA Phase 1, Open Label, Dose Characteristic Study to Investigate the Pharmacokinetics, Pharmacodynamics, Safety, and Tolerability of Intravenous and Subcutaneous Doses of GSK2315698A in Patients With Systemic AmyloidosisAmyloidosisDrug: GSK2315698GlaxoSmithKlineNULLCompleted18 Years80 YearsAll17Phase 1United Kingdom