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MaxCyte Inks Platform License With Vertex For Gene-Editing Program For Rare Blood Disorders

MaxCyte Inks Platform License With Vertex For Gene-Editing Program For Rare Blood Disorders

Maxcell Inks平台许可Vertex用于罕见血液疾病的基因编辑程序
Benzinga Real-time News ·  2022/09/28 12:42

MaxCyte Inc (NASDAQ:MXCT) has signed a strategic platform license with Vertex Pharmaceuticals Incorporated (NASDAQ:VRTX).

Maxcell Inc.(纳斯达克股票代码:MXCT)与中国移动签署战略平台许可证Vertex制药公司(纳斯达克:VRTX)。

  • Under the terms of the agreement, Vertex obtains non-exclusive clinical and commercial rights to use MaxCyte's Flow Electroporation technology and ExPERT platform in developing its CRISPR/Cas9-based gene-edited therapy (exa-cel, formerly known as CTX001).
  • MaxCyte is entitled to receive platform licensing fees and program-related revenue.
  • Exa-cel is an investigational ex vivo CRISPR gene-edited cell therapy for transfusion-dependent beta-thalassemia (TDT) or sickle cell disease (SCD).
  • The same MaxCyte technology was used in the development of exa-cel under an agreement between MaxCyte and CRISPR Therapeutics AG (NASDAQ:CRSP).
  • On Tuesday, the FDA granted exagamglogene autotemcel (exa-cel) a rolling review for the potential treatment of sickle cell disease (SCD) and transfusion-dependent beta-thalassemia (TDT).
  • Vertex will submit its biologics licensing application for exa-cel, beginning in November, and expects to complete the submission by the end of the first quarter of 2023.
  • The company is on track to submit marketing applications to the European Medicines Agency by the end of the year.
  • Price Action: MXCT shares are up 10.2% at $6.40 on the last check Wednesday.
  • 根据协议条款,Vertex获得了使用MaxCyte的流动电穿孔技术和专家平台开发其基于CRISPR/Cas9的基因编辑疗法(Exacel,以前称为CTX001)的非独家临床和商业权利。
  • Maxcell有权获得平台许可费和节目相关收入。
  • Exa-cel是一个调查性的离体CRISPR基因编辑细胞疗法用于输血依赖型β-地中海贫血(TDT)或镰状细胞病(SCD)。
  • 根据MaxCyte和Exacel之间的协议,在Exacel的开发中使用了相同的MaxCyte技术CRISPR治疗公司(纳斯达克:CRSP)。
  • 周二,FDA批准了exagamlobgene autemcel(exa-cel)对镰状细胞病(SCD)和输血依赖型β地中海贫血(TDT)的潜在治疗进行滚动审查。
  • Vertex将从11月开始提交生物制品出口许可申请,预计在2023年第一季度末完成提交。
  • 该公司有望在今年年底前向欧洲药品管理局提交营销申请。
  • 价格行动:MXCT股价周三尾盘上涨10.2%,至6.40美元。
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