MAS-825(MAS-825) - 药物靶点：IL-18 x IL-1β_在研适应症：冠状动脉疾病，化脓性汗腺炎，婴幼儿小肠结肠炎自身炎症_专利_临床

概要

基本信息

药物类型

双特异性抗体

别名

靶点

IL-18 x IL-1β

作用机制

IL-18抑制剂(白细胞介素18抑制剂)、IL-1β抑制剂(白细胞介素-1β抑制剂)

治疗领域

免疫系统疾病感染心血管疾病+ [5]

在研适应症

冠状动脉疾病化脓性汗腺炎婴幼儿小肠结肠炎自身炎症+ [2]

非在研适应症

新型冠状病毒感染呼吸功能不全

原研机构

Novartis Pharmaceuticals Corp.

在研机构

Novartis Pharmaceuticals Corp.

Novartis AG

非在研机构-

最高研发阶段临床2期

首次获批日期-

最高研发阶段(中国)-

特殊审评-

登录后查看时间轴

关联

6

项与 MAS-825 相关的临床试验

NCT06097663

/ Completed临床2期

A Randomized, Placebo-controlled, Parallel-group, Investigator- and Participant-blinded Phase 2a Study to Investigate the Efficacy, Safety, and Tolerability of DFV890 and MAS825 for Inflammatory Marker Reduction in an Adult Population With Coronary Heart Disease and Clonal Hematopoiesis of Indeterminate Potential (CHIP)

This Phase 2a clinical trial will evaluate the effectiveness, safety, and tolerability of increasing dose strengths of an oral daily medication, DFV890, administered for 12 weeks, or a single s.c. dose of MAS825, to reduce key markers of inflammation related to CVD risk, such as IL-6 and IL-18, in approximately 28 people with known coronary heart disease and TET2 or DNMT3A CHIP (VAF ≥2%).

开始日期2024-02-15

申办/合作机构

Novartis Pharmaceuticals Corp.

NCT06309823

/ Completed临床3期IIT

A Single-patient Clinical Trial of MAS825 in a Patient With XIAP Deficiency

MAS825 is a bi-specific IgG1 monoclonal antibody that simultaneously targets IL-1 beta and IL-18, thereby neutralizing both cytokines that are thought to be integral to the pathogenesis of XLP-2. Clinical trials are currently examining its efficacy in other diseases associated with elevations of these cytokines, including NLRC4-associated disease and hidradenitis suppurativa. This study proposes to assess the effectiveness of MAS825 in a single patient with XLP-2, who has previously demonstrated response to blockade of IL-1 beta and IL-18. Given the lack of alternative pharmaceutical options for XLP-2, this represents the only known medication option that avoids the toxicity associated with high-dose corticosteroids and the morbidity associated with hematopoietic stem cell transplantation.

开始日期2023-02-08

申办/合作机构

The Hospital for Sick Children

NCT04641442

/ Active, not recruiting临床2期

A Three-period Multicenter Study, With a Randomized-withdrawal, Double-blind, Placebo-controlled Design to Evaluate the Clinical Efficacy, Safety and Tolerability of MAS825 in Patients With Monogenic IL-18 Driven Autoinflammatory Diseases, Including NLRC4-GOF, XIAP Deficiency, or CDC42 Mutations

This study is a Phase 2 trial designed to evaluate the clinical efficacy, safety, and tolerability of MAS825 in patients with NLRC4-GOF, XIAP deficiency, or CDC42 mutations.

开始日期2020-12-18

申办/合作机构

Novartis Pharmaceuticals Corp.

100 项与 MAS-825 相关的临床结果

登录后查看更多信息

100 项与 MAS-825 相关的转化医学

登录后查看更多信息

100 项与 MAS-825 相关的专利（医药）

登录后查看更多信息

4

项与 MAS-825 相关的文献（医药）

2024-04-02·Rheumatology

Experience of anti-IL-1β and anti-IL-18 combined therapy (MAS825) in recurrent and recalcitrant macrophage activation syndrome

Article

作者: Sözeri, Betül ; Ulu, Kadir ; Çağlayan, Şengül

2023-10-13·Clinical and experimental immunology

Efficacy and safety of MAS825 (anti-IL-1β/IL-18) in COVID-19 patients with pneumonia and impaired respiratory function.

Article

作者: O'Neal, Hollis R ; Hakim, Alex D ; Awili, Mustafa ; Yu, Lili ; Junge, Guido ; Overcash, Jeffrey S ; Jenkins, Janet ; Sengupta, Tirtha ; Watts, Jen ; Lee, Richard ; Bendrick-Peart, Jamie ; Stein, Richard R ; Rowlands, Marianna ; Chauffe, Ann ; Siddiqi, Omar ; Matthews, Jesse ; Patel, Bela ; Kiffe, Michael ; Koo, Philip ; Pachori, Alok ; Waters, Michael ; Hammond, Terese C ; Pinck, Anne ; Jaffrani, Naseem ; Levitch, Rafael ; Waldron-Lynch, Frank ; Criner, Gerard J

MAS825, a bispecific IL-1β/IL-18 monoclonal antibody, could improve clinical outcomes in COVID-19 pneumonia by reducing inflammasome-mediated inflammation. Hospitalized non-ventilated patients with COVID-19 pneumonia (n = 138) were randomized (1:1) to receive MAS825 (10 mg/kg single i.v.) or placebo in addition to standard of care (SoC). The primary endpoint was the composite Acute Physiology and Chronic Health Evaluation II (APACHE II) score on Day 15 or on the day of discharge (whichever was earlier) with worst-case imputation for death. Other study endpoints included safety, C-reactive protein (CRP), SARS-CoV-2 presence, and inflammatory markers. On Day 15, the APACHE II score was 14.5 ± 1.87 and 13.5 ± 1.8 in the MAS825 and placebo groups, respectively (P = 0.33). MAS825 + SoC led to 33% relative reduction in intensive care unit (ICU) admissions, ~1 day reduction in ICU stay, reduction in mean duration of oxygen support (13.5 versus 14.3 days), and earlier clearance of virus on Day 15 versus placebo + SoC group. On Day 15, compared with placebo group, patients treated with MAS825 + SoC showed a 51% decrease in CRP levels, 42% lower IL-6 levels, 19% decrease in neutrophil levels, and 16% lower interferon-γ levels, indicative of IL-1β and IL-18 pathway engagement. MAS825 + SoC did not improve APACHE II score in hospitalized patients with severe COVID-19 pneumonia; however, it inhibited relevant clinical and inflammatory pathway biomarkers and resulted in faster virus clearance versus placebo + SoC. MAS825 used in conjunction with SoC was well tolerated. None of the adverse events (AEs) or serious AEs were treatment-related.

2023-01-01·Journal of Clinical Immunology

Improvement of Refractory Systemic Juvenile Idiopathic Arthritis-Associated Lung Disease with Single-Agent Blockade of IL-1β and IL-18

Article

作者: Josephson, Maureen B ; Rood, Julia E ; Burnham, Jon M ; Behrens, Edward M ; Pogoriler, Jennifer ; Finn, Laura S ; Canna, Scott W ; Bar-Or, Amit ; Rezk, Ayman

Systemic juvenile idiopathic arthritis associated with interstitial lung disease (SJIA-LD) represents a highly morbid subset of SJIA for which effective therapies are lacking. We report the case of a patient with refractory SJIA-LD who underwent treatment with MAS-825, an investigational bispecific monoclonal antibody targeting IL-1β and IL-18. MAS-825 treatment was associated with a marked reduction in total IL-18 and free IL-18 in both serum and bronchoalveolar lavage fluid (BAL). Baseline oxygen saturation, exercise tolerance, and quality of life metrics improved after treatment with MAS-825, while pulmonary function testing remained stable. Following treatment, the BAL showed no evidence of pulmonary alveolar proteinosis and inflammatory infiltrates were markedly reduced, reflected by decreased numbers of CD4 T-cells, CD8 T-cells, and macrophages. The patient was able to wean entirely off systemic corticosteroids and other biologics after 10 months of treatment with MAS-825 and experienced no side effects of the drug. This case demonstrates improvement in pulmonary symptoms, lung inflammation, and burden of immunomodulatory therapy after treatment with MAS-825 and suggests that simultaneous targeting of both IL-1β and IL-18 may be a safe and effective treatment strategy in SJIA-LD.

100 项与 MAS-825 相关的药物交易

登录后查看更多信息

研发状态

10 条进展最快的记录,

登录

后查看更多信息

适应症	最高研发状态	国家/地区	公司	日期
婴幼儿小肠结肠炎自身炎症	临床2期	英国	Novartis Pharmaceuticals Corp.	2020-12-18
自身炎症性疾病	临床2期	美国	Novartis Pharmaceuticals Corp.	2020-12-18
自身炎症性疾病	临床2期	法国	Novartis Pharmaceuticals Corp.	2020-12-18
自身炎症性疾病	临床2期	英国	Novartis Pharmaceuticals Corp.	2020-12-18
自身炎症性疾病	临床2期	意大利	Novartis Pharmaceuticals Corp.	2020-12-18
自身炎症性疾病	临床2期	日本	Novartis Pharmaceuticals Corp.	2020-12-18
自身炎症性疾病	临床2期	西班牙	Novartis Pharmaceuticals Corp.	2020-12-18
自身炎症性疾病	临床2期	捷克	Novartis Pharmaceuticals Corp.	2020-12-18
新型冠状病毒感染	临床前	美国	Novartis Pharmaceuticals Corp.	2020-06-11
呼吸功能不全	临床前	美国	Novartis Pharmaceuticals Corp.	2020-06-11

登录后查看更多信息

临床结果

适应症

分期

评价

查看全部结果

研究	分期	人群特征	评价人数	分组	结果	评价	发布日期


NCT04382651 (MAS825, Pubmed \| Clin Exp Immunol)	临床2期	呼吸功能不全 C-reactive protein (CRP) \| SARS-CoV-2 presence \| inflammatory markers	138	MAS825	壓艱網鏇衊艱簾蓋憲顧(鏇淵餘膚顧鬱淵範製獵) = None of the adverse events (AEs) or serious AEs were treatment-related 鑰鏇製廠鏇糧蓋鹽鏇憲 (襯選蓋選選齋鏇願齋壓 ) 更多	积极	2023-10-13
				Placebo
NCT04382651 (MAS-COVID \| MAS825, CTgov)	临床2期	新型冠状病毒感染 \| 呼吸功能不全	140	Standard of Care (SoC)+MAS825 (MAS825 + SoC)	範廠鹹觸鏇鬱餘廠積選(窪製餘繭夢膚選襯鏇遞) = 構願糧遞衊憲夢簾製鹹憲網齋醖膚廠選艱鑰選 (鹹窪壓襯積遞遞艱壓簾, 鹽夢鹽醖餘築窪範壓襯 ~ 願鹽鏇積範淵蓋製壓膚) 更多	-	2022-04-20
				Placebo (Placebo + SoC)	範廠鹹觸鏇鬱餘廠積選(窪製餘繭夢膚選襯鏇遞) = 鑰繭齋衊壓壓糧觸襯範憲網齋醖膚廠選艱鑰選 (鹹窪壓襯積遞遞艱壓簾, 窪製選齋艱築鑰廠襯簾 ~ 鏇齋醖憲願鏇廠鹽積遞) 更多