QurientPress Release


 

Press Release

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    • Qurient Announces U.S. FDA Clearance of IND Application for …

      Phase 1/2 clinical study in patients with advanced solid tumor expected to start in 2Q2022 SEONGNAM-SI, South Korea--(BUSINESS WIRE)--Qurient Co. Ltd. (KRX: 115180), a clinica....Article Source : Businesswire
      Link : https://www.businesswire.com/news/home/20220208005826/en/Qurient-Announces-U.S.-FDA-Clearance-of-IND-Application-for-Q901-a-Novel-Cancer-Therapy

      Date
      2022-02-08
      Author
      QURIENT
  • 105
    • 큐리언트, 항암치료제 Q901 미국 FDA에 임상 1/2상 신청

      큐리언트는 6일 CDK7 억제 기전의 항암치료제 Q901의 미국 임상을 위해 식품의약국(FDA)에 임상 1/2상 시험을 신청했다고 공시했다. Q901은 세포 주기 조절 인자(Cell cycle regulator) 중 핵심이 되는 CDK7을 저해하는 항암제다. 경쟁약물 대비 월등한 선택성으로 기전적, 효능적 차별성을 ....

      Date
      2022-01-06
      Author
      QURIENT
  • 104
  • 103
    • Qurient Announces Collaboration Agreement with MSD to Evalua…

      Article Source : Business Wire
      Link : https://www.businesswire.com/news/home/20211122006506/en/Qurient-Announces-Collaboration-Agreement-with-MSD-to-Evaluate-Selective-Triple-Inhibitor-Q702-in-Combination-With-KEYTRUDA%C2%AE-pembrolizumab

      Date
      2021-11-23
      Author
      QURIENT
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