Invivoscribe Announces Key Submission in the EU, Expanded Presence and Activity in China

invivoscribe announces key submission in the eu expanded presence and activity in china

Sumary of Invivoscribe Announces Key Submission in the EU, Expanded Presence and Activity in China:

  • The LeukoStrat® CDx FLT3 Mutation Assay was used to select patients in a Phase III drug trial resulting in the NMPA/CDE February 2021 conditional approval of the Astellas drug gilteritinib fumarate used to treat R/R FLT3+ AML patients.
  • Invivoscribe also has a significant impact on global health working with pharmaceutical companies to accelerate approvals of new drugs and treatments by supporting international clinical trials, developing, commercializing companion diagnostics, and providing expertise in both regulatory and laboratory services.

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