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BioCryst Presents Results on HAE Treatment and Patient Care at Global Symposium

BioCryst Presents Results on HAE Treatment and Patient Care at Global Symposium

生物晶体在全球货币研讨会上介绍HAE治疗和患者护理结果
Benzinga ·  09/06 03:02

BioCryst Pharmaceuticals, Inc. (Nasdaq: BCRX) today announced the presentation of six posters, including the first interim real-word evidence from the APeX-N trial, and new data highlighting the value of shared decision making (SDM) between healthcare providers (HCPs) and their hereditary angioedema (HAE) patients to provide optimal patient outcomes.

BioCryst Pharmaceuticals, Inc.(纳斯达克:BCRX)今天宣布展示了六张海报,包括APeX-N试验的首个中期真实世界证据,以及突出展示医疗保健提供者(HCP)与遗传性血管性水肿(HAE)患者之间共享决策(SDM)的价值,以实现最佳患者结局。

The company is presenting the posters at the 7th Bradykinin Symposium in Berlin from September 5-6, 2024.

该公司将在2024年9月5日至6日于柏林举行的第7届激肽酶抑制剂研讨会上展示这些海报。

  • APeX-N interim results: Oral berotralstat for HAE prophylaxis in Europe
  • HCP and patient perspectives: HAE long-term prophylaxis and shared decision-making
  • Adverse health outcomes and perspectives of androgen use in HAE
  • Evaluation of adherence to berotralstat in patients with hereditary angioedema
  • Tolerability and effectiveness of berotralstat for long-term prophylaxis in HAE
  • Effectiveness and safety of berotralstat in HAE with normal C1-inhibitor
  • APeX-N中期结果:欧洲遗传性血管性水肿(HAE)口服berotralstat预防
  • HCP和患者的观点:HAE长期预防和共同决策
  • HAE雄激素使用的不良健康结果和观点
  • 评估遗传性血管性水肿患者对berotralstat的依从性
  • HAE的长期预防中berotralstat的耐受性和有效性
  • HAE合并正常C1抑制蛋白时berotralstat的有效性和安全性

APeX-N interim results

APeX-N中期结果

APeX-N is a European multi-center observational study assessing the safety (primary objective), effectiveness and quality of life (secondary objectives) of berotralstat 150 mg in routine clinical use. This interim analysis included 56 patients from the United Kingdom, France, Germany and Sweden.

APeX-N是一项欧洲多中心观察研究,评估berotralstat在常规临床使用中的安全性(主要目标)、有效性和生活质量(次要目标)。这次中期分析包括来自英国、法国、德国和瑞典的56名患者。

Non-serious gastrointestinal adverse events were reported in 12.5 percent of patients. Seven percent (n=4) of patients discontinued treatment (three due to unsatisfactory response, one to participate in a clinical trial). One patient had a severe HAE attack but continued treatment.

12.5%的患者报告非严重胃肠道不良事件。7%的患者(n=4)中止治疗(其中三人由于治疗效果不佳,一人参与临床试验)。一名患者发生了严重HAE发作,但继续治疗。

"These initial data from APeX-N in Europe reinforce and closely replicate the clinical trial and real-world evidence of berotralstat as the first oral prophylaxis for HAE," said Dr. Sorena Kiani, consultant immunologist at Royal Free London NHS Foundation.

这些来自欧洲APeX-N的初步数据证实并紧密复制了berotralstat作为HAE的首个口服预防措施的临床试验和真实世界证据,皇家自由伦敦NHS基金会的免疫学顾问Sorena Kiani博士说。

HCP and patient perspectives: HAE long-term prophylaxis and shared decision-making

HCP和患者的观点:HAE长期预防和共同决策

This study, conducted in Germany, explored the dynamics between HCPs and patients in HAE management, identifying barriers to SDM and strategies to improve it. Ten HCPs participated in 60 minute interviews and simulated patient consultations. Eight HAE patients participated in 30 minute interviews. Participants then convened in structured focus groups to discuss their findings.

这项在德国进行的研究探讨了HCP和患者在HAE管理中的动态,并确定了SDm的障碍和改进策略。十名HCP参加了60分钟的面试和模拟患者咨询。八名HAE患者参加了30分钟的面试。参与者随后召开结构化的焦点小组讨论他们的发现。

The participants identified a need for enhanced HCP awareness of patient perspectives, more comprehensive HCP-patient conversations and improved education about HAE treatment management.

参与者发现HCP需要增加对患者观点的认识,进行更全面的HCP-患者交流,并改善有关HAE治疗管理的教育。

"The findings from this study support the need for further insights to develop future guidance and HAE management strategies to facilitate successful shared decision making and improved patient quality of life," said Dr. Emel Aygören-Pürsün, department for children and adolescents, University Hospital Frankfurt, Germany.

这项研究的发现支持了进一步洞察以制定未来的指导和HAE管理策略,以促进成功的共享决策和改善患者的生活质量,德国法兰克福大学医院儿童和青少年部门的Emel Aygören-Pürsün博士表示。

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