Xiaoyan Yu , Qian Li , Doudou Zhang , Kangping Guo , Wei Sun , Wenqiao Huang , Li Gao , Rongmei Yan , Lihong Yun , Jun Wan , Ting Xu , Pilin Wang
{"title":"kn060 -一种同时靶向FXI-A2/A3表位的人源化双域抗体:开拓性的抗凝血因子XI策略治疗材料性高血压-来自临床前模型的证据。","authors":"Xiaoyan Yu , Qian Li , Doudou Zhang , Kangping Guo , Wei Sun , Wenqiao Huang , Li Gao , Rongmei Yan , Lihong Yun , Jun Wan , Ting Xu , Pilin Wang","doi":"10.1016/j.ejphar.2025.178171","DOIUrl":null,"url":null,"abstract":"<div><div>Growing evidence positions Factor XI (FXI) as a promising anticoagulation target, where its role in pathological thrombus formation significantly outweighs its contribution to physiological hemostasis. This distinctive pathophysiological profile has propelled FXI inhibition as a transformative therapeutic paradigm, with multiple candidates in Phase I-III trials spanning venous thromboembolism prophylaxis to arterial thrombosis prevention. Building on emerging insights into FXI-mediated vascular inflammation and remodeling, we herein unveil the first preclinical evidence supporting KN060—a humanized dual-domain antibody simultaneously targeting FXI-A2/A3 epitopes—as a novel antihypertensive agent. In angiotensin II-challenged mice, 5-week KN060 monotherapy (10 mg/kg triweekly) elicited sustained systolic blood pressure (SBP) reduction of 27.8 mmHg (120.7 mmHg in KN060 group vs 148.5 mmHg in vehicle control group). Furthermore, in spontaneously hypertensive rats, 9-week KN060 monotherapy (15 mg/kg twice weekly) achieved sustained SBP reduction of 34.7 mmHg (172.2 mmHg in KN060 group vs 206.9 mmHg in vehicle control group), concomitantly reducing left ventricular mass (0.67 g vs 0.773 g) and aortic relative media thickness (28.74 vs 31.59). Notably, co-administration of KN060 (3 mg/kg) with losartan (5 mg/kg) in SHRs demonstrated synergistic efficacy, achieving greater SBP reduction than losartan monotherapy (ΔSBP: −23.7 mmHg vs −15.9 mmHg). These findings establish KN060 as a first-in-class therapeutic bridging anticoagulation and vascular protection. Its unique bispecific architecture enables near-complete FXI activity inhibition while preserving hemostatic capacity, addressing critical limitations of conventional RAAS blockers in resistant hypertension. With an ongoing Phase Ib trial in primary hypertension patients (NMPA approval No CXSL2400827), KN060 emerges as a transformative candidate for precision management of hypertension.</div></div>","PeriodicalId":12004,"journal":{"name":"European journal of pharmacology","volume":"1006 ","pages":"Article 178171"},"PeriodicalIF":4.7000,"publicationDate":"2025-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"KN060-a humanized dual-domain antibody simultaneously targeting FXI-A2/A3 epitopes: Pioneering the anti-coagulation factor XI strategy for Aterial hypertension – Evidence from preclinical models\",\"authors\":\"Xiaoyan Yu , Qian Li , Doudou Zhang , Kangping Guo , Wei Sun , Wenqiao Huang , Li Gao , Rongmei Yan , Lihong Yun , Jun Wan , Ting Xu , Pilin Wang\",\"doi\":\"10.1016/j.ejphar.2025.178171\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Growing evidence positions Factor XI (FXI) as a promising anticoagulation target, where its role in pathological thrombus formation significantly outweighs its contribution to physiological hemostasis. This distinctive pathophysiological profile has propelled FXI inhibition as a transformative therapeutic paradigm, with multiple candidates in Phase I-III trials spanning venous thromboembolism prophylaxis to arterial thrombosis prevention. Building on emerging insights into FXI-mediated vascular inflammation and remodeling, we herein unveil the first preclinical evidence supporting KN060—a humanized dual-domain antibody simultaneously targeting FXI-A2/A3 epitopes—as a novel antihypertensive agent. In angiotensin II-challenged mice, 5-week KN060 monotherapy (10 mg/kg triweekly) elicited sustained systolic blood pressure (SBP) reduction of 27.8 mmHg (120.7 mmHg in KN060 group vs 148.5 mmHg in vehicle control group). Furthermore, in spontaneously hypertensive rats, 9-week KN060 monotherapy (15 mg/kg twice weekly) achieved sustained SBP reduction of 34.7 mmHg (172.2 mmHg in KN060 group vs 206.9 mmHg in vehicle control group), concomitantly reducing left ventricular mass (0.67 g vs 0.773 g) and aortic relative media thickness (28.74 vs 31.59). Notably, co-administration of KN060 (3 mg/kg) with losartan (5 mg/kg) in SHRs demonstrated synergistic efficacy, achieving greater SBP reduction than losartan monotherapy (ΔSBP: −23.7 mmHg vs −15.9 mmHg). These findings establish KN060 as a first-in-class therapeutic bridging anticoagulation and vascular protection. Its unique bispecific architecture enables near-complete FXI activity inhibition while preserving hemostatic capacity, addressing critical limitations of conventional RAAS blockers in resistant hypertension. With an ongoing Phase Ib trial in primary hypertension patients (NMPA approval No CXSL2400827), KN060 emerges as a transformative candidate for precision management of hypertension.</div></div>\",\"PeriodicalId\":12004,\"journal\":{\"name\":\"European journal of pharmacology\",\"volume\":\"1006 \",\"pages\":\"Article 178171\"},\"PeriodicalIF\":4.7000,\"publicationDate\":\"2025-09-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"European journal of pharmacology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0014299925009252\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"European journal of pharmacology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0014299925009252","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
KN060-a humanized dual-domain antibody simultaneously targeting FXI-A2/A3 epitopes: Pioneering the anti-coagulation factor XI strategy for Aterial hypertension – Evidence from preclinical models
Growing evidence positions Factor XI (FXI) as a promising anticoagulation target, where its role in pathological thrombus formation significantly outweighs its contribution to physiological hemostasis. This distinctive pathophysiological profile has propelled FXI inhibition as a transformative therapeutic paradigm, with multiple candidates in Phase I-III trials spanning venous thromboembolism prophylaxis to arterial thrombosis prevention. Building on emerging insights into FXI-mediated vascular inflammation and remodeling, we herein unveil the first preclinical evidence supporting KN060—a humanized dual-domain antibody simultaneously targeting FXI-A2/A3 epitopes—as a novel antihypertensive agent. In angiotensin II-challenged mice, 5-week KN060 monotherapy (10 mg/kg triweekly) elicited sustained systolic blood pressure (SBP) reduction of 27.8 mmHg (120.7 mmHg in KN060 group vs 148.5 mmHg in vehicle control group). Furthermore, in spontaneously hypertensive rats, 9-week KN060 monotherapy (15 mg/kg twice weekly) achieved sustained SBP reduction of 34.7 mmHg (172.2 mmHg in KN060 group vs 206.9 mmHg in vehicle control group), concomitantly reducing left ventricular mass (0.67 g vs 0.773 g) and aortic relative media thickness (28.74 vs 31.59). Notably, co-administration of KN060 (3 mg/kg) with losartan (5 mg/kg) in SHRs demonstrated synergistic efficacy, achieving greater SBP reduction than losartan monotherapy (ΔSBP: −23.7 mmHg vs −15.9 mmHg). These findings establish KN060 as a first-in-class therapeutic bridging anticoagulation and vascular protection. Its unique bispecific architecture enables near-complete FXI activity inhibition while preserving hemostatic capacity, addressing critical limitations of conventional RAAS blockers in resistant hypertension. With an ongoing Phase Ib trial in primary hypertension patients (NMPA approval No CXSL2400827), KN060 emerges as a transformative candidate for precision management of hypertension.
期刊介绍:
The European Journal of Pharmacology publishes research papers covering all aspects of experimental pharmacology with focus on the mechanism of action of structurally identified compounds affecting biological systems.
The scope includes:
Behavioural pharmacology
Neuropharmacology and analgesia
Cardiovascular pharmacology
Pulmonary, gastrointestinal and urogenital pharmacology
Endocrine pharmacology
Immunopharmacology and inflammation
Molecular and cellular pharmacology
Regenerative pharmacology
Biologicals and biotherapeutics
Translational pharmacology
Nutriceutical pharmacology.