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迈威生物创新品种 7MW4811 亮相第 15 届 World ADC 大会

ID: 52286
description:
上海2024年11月8日 /美通社/ -- 迈威生物(688062.SH),一家全产业链布局的创新型生物制药公司,2024 年 11 月 4 至 7 日在第 15 届世界抗体药物偶联大会(World ADC San Diego)以壁报形式发表了主题为 “Preclinical Development of 7MW4811, an MtoxinTM (MF6)-based Antibody-drug Conjugate for the Treatment of Solid Tumors” 的最新研究,展示了基于新一代 ADC 技术平台 IDDCTM 开发的 ADC 创新药 7MW4811 针对实体瘤的临床前研究进展。 研究结果表明,7MW4811 在包括肺癌、结直肠癌、胰腺癌和胃癌在内的多种癌症中表现出了广泛而优异的抗肿瘤效果,尤其在胃肠道肿瘤方面具备巨大治疗潜力。 IDDCTM 是一项经过临床验证的定点偶联技术,构建的 ADC 具有良好的均一性、有效性以及安全性优势。新型载荷 MtoxinTM(MF6)具有良好的药效、旁观者杀伤效果,以及抗多药耐药等优势。 关于迈威生物 迈威生物 (688062.SH) 是一家全产业链布局的创新型生物制药公司,始终秉承“让创新从梦想变成现实”的愿景,践行“探索生命,惠及健康”的使命,通过源头创新,为患者提供疗效更好、可及性更强的生物创新药,满足全球未被满足的临床需求。2017 年成立以来,迈威生物构建了以抗体药物靶点发现与分子发现为起点,覆盖成药性研究、临床前研究、临床研究和生产转化等药品研发全周期的创新体系,实现集研发、生产、营销于一体的全产业链布局。我们专注于肿瘤和年龄相关疾病,涉及肿瘤、自身免疫、骨疾病、眼科、血液、感染等治疗领域,凭借国际领先的特色技术平台和研发创新能力,建立了丰富且具有竞争力的管线。现有 15 个品种处于不同阶段,包括 11 个创新品种和 4 个生物类似药,其中 3 个品种上市,1 个品种药品上市许可申请已获受理,3 个品种处于关键注册临床试验阶段。并独立承担 1 项国家“重大新药创制”重大科技专项、2 项国家重点研发计划和多个省市级科技创新项目。迈威生物以创新为本,注重产业转化,符合中国 NMPA、美国 FDA、欧盟 EMA GMP标准的抗体和重组蛋白药物产业化基地已在江苏泰州投入使用,并已通过欧盟 QP 审计,位于上海金山和江苏泰州的大规模商业化生产基地正在建设中。欲了解更多信息,请访问:www.mabwell.com。 前瞻性声明 本新闻稿所发布的信息中可能会包含某些前瞻性表述。这些表述本质上具有相当风险和不确定性。在使用“预期”、“相信”、“预测”、“期望”、“打算”及其他类似词语进行表述时,凡与本公司有关的,目的均是要指明其属前瞻性表述。本公司并无义务不断地更新这些预测性陈述。 这些前瞻性表述乃基于本公司管理层在做出表述时对未来事务的现有看法、假设、期望、估计、预测和理解。这些表述并非对未来发展的保证,会受到风险、不确性及其他因素的影响,有些乃超出本公司的控制范围,难以预计。因此,受我们的业务、竞争环境、政治、经济、法律和社会情况的未来变化及发展的影响,实际结果可能会与前瞻性表述所含资料有较大差别。 本公司、本公司董事及雇员代理概不承担 (a) 更正或更新本网站所载前瞻性表述的任何义务;及 (b) 若因任何前瞻性表述不能实现或变成不正确而引致的任何责任。
Publication date:
2024-11-08 02:00:00
Source ID:
prnasia
Article ID:
e86ccefa4d6175b08082808087fefd54
Link:
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Country (The country of the publisher):
Cambodia (cambodia (kh))
Indonesia (indonesia (id))
Macau (macau (mo))
Brunei (brunei (bn))
Hong Kong (hong kong (hk))
Taiwan (taiwan (tw))
Philippines (philippines (ph))
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Language (The language of the news article):
chinese ()
Category(s):
Health
Keywords:
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