DNA:要产生mRNA,需要一个DNA模板。生物制药行业将质粒用于此目的。只有一小部分质粒DNA编码有关感兴趣的相关蛋白质,例如g。 SARS-COV-2的尖峰蛋白。大多数质粒用于将DNA塑造成所需的环形式。环形对于相关DNA序列的扩增至关重要。
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ICR Consilium Chris Gardner, David Daley, Lindsey Neville Tel: +44 (0) 20 3709 5700 Email: arecor@consilium-comms.com Notes to Editors About Arecor Arecor Therapeutics plc is a globally focused biopharmaceutical company transforming patient care by bringing innovative medicines to market through the enhancement of existing therapeutic products.通过应用我们创新的专有技术平台Arestat™,我们正在开发糖尿病和其他指示中专有产品的内部投资组合,并与领先的药品和生物技术公司合作以提供治疗产品。Arestat™平台由广泛的专利组合支持。该协作增加了雷科尔(Arecor)的广泛集中活动计划,其两个主要专有临床开发计划(AT278和AT247)是两个超优化的胰岛素候选者,这些胰岛素候选者提供了简化和改善糖尿病的人的血液葡萄糖控制的潜力
The board of directors (the “ Board ”) of Sino Biopharmaceutical Limited (the “ Company ”, together with its subsidiaries, the “ Group ”) announced that KRAS G12C Inhibitor “Garsorasib Tablet (D- 1553)”, which is jointly developed by the Group, has been included in the Breakthrough Therapeutic Designation (BTD) process by the Center for Drug Evaluation (CDE) of the National Medical Products Administration中国。总共有两个指示:1)用于治疗一线治疗失败的患者的局部晚期或转移性胰管导管腺癌和KRAS G12C突变;和2)与二妥昔单抗注射术治疗KRAS G12C突变阳性和外科手术无法切除的局部晚期或转移性结直肠癌的患者(包括二线标准疗法失败的患者)(包括oxaliplatin,Irinotecan,Irinotecan,5-fluorouraracil,5-氟尿嘧啶,5-氟尿嘧啶,抗vegfff Monoclonal Antoclonal antibody)。
配体制药公司持有其内部投资团队审查的收入,皇室和石头产生资产的投资组合。配体在其机会设置中考虑了单个的生物制药产品,平台,公司和收入来源。进行投资时,它针对后期和商业收入的资产。该公司拥有多元化的生物制药特许权使用费,这是一种溶解和稳定代理商,以及其他公司的股权和股权和所有者,包括Primrose,Palvella,Viking和Pelthos。版税投资组合由12个主要的商业舞台资产和> 90个活跃计划组成。除了确定的计划外,配体计划每年部署约2亿美元,以获取新的资产,这些资产可以在很大程度上以自由现金流资金进行资金。公司经验丰富的投资团队在潜在客户的数据中签订了保密协议的内部外观,从而获得了较高的风险调整后收益。除了其主要的商业资产外,配体的开发阶段计划组合以及由内部资本资本资助的未来收购还可以促进长期收入增长并产生较高的风险调整后收益。
The board of directors (the “ Board ”) of Sino Biopharmaceutical Limited (the “ Company ”, together with its subsidiaries, the “ Group ”) announces that the phase III clinical study(ALTN-III-04)of Anlotinib Hydrochloride Capsule, a Category 1 innovative drug self-developed by the Group, in combination with chemotherapy for the first-line treatment of advanced unresectable or转移性软组织肉瘤已通过独立数据监测委员会(IDMC)完成了协议规定的临时分析,确定主要研究终点无进展生存率(PFS)符合协议的预定义优势阈值,并且次要端点总生存率(OS)的总体生存率(OS)呈良好的趋势。该小组已与中国国家医疗产品管理局的药物评估中心(CDE)有关此适应症的营销申请,并获得了CDE的同意,以提交营销申请,以提交此额外的一线盐酸盐氯化物盐和化学疗法的一线指示。小组将在不久的将来提交营销申请。
DBV Technologies to Participate in Upcoming AAAAI/WAO Joint Congress DBV Technologies (Euronext: DBV – ISIN: FR0010417345 – Nasdaq Stock Market: DBVT), a clinical-stage biopharmaceutical company, today announced that the company will participate in the American Academy of Allergy, Asthma, and Immunology and World Allergy Organization (AAAAI/WAO)联合国会,2月28日,3月3日,2025年3月3日,位于加利福尼亚州圣地亚哥。An oral abstract presentation by Dr. David Fleischer, FAAAAI, FACAAI, Professor of Pediatrics at Children's Hospital Colorado, will describe Month 60 (M60), end-of- study efficacy and safety results from PEOPLE (the open-label extension of the 12- month, double-blind placebo-controlled, Phase 3 PEPITES study in peanut allergic children aged 4-11 years).所有参加人员的合格参与者均接受了Viaskin®Peanut补丁长达60个月的治疗。演示文稿中的要点包括: