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FDA Grants Fast Track Designation for LYT-200 to Treat Head and Neck Cancers

Treatment with LYT-200 is currently being assessed in a phase 1/2 adaptive design trial in advanced/metastatic solid tumors and in a phase 1b clinical trial.

Aleksandra filipovicDeric shermanAbbvie incPuretech healthMemorial sloan kettering cancer centerNational cancer instituteFast trackTech receivesTrack designation

FDA Grants PRTC s LYT-200 Fast Track Designation | Company Announcement

Investegate announcements from FDA Grants PRTC's LYT-200 Fast Track Designation

United kingdomNichole bobbynAleksandra filipovicBen atwellDeric shermanRob winderDrug administrationMemorial sloan kettering cancer centerPuretech healthTech healthTrack designationUnited statesfoodFast trackOncologyat puretechFounded entity gallopFounded entities

PureTech Receives FDA Fast Track Designation for LYT-200 in Head and Neck Cancers

PureTech Receives FDA Fast Track Designation for LYT-200 in Head and Neck Cancers
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United kingdomBen atwellNichole bobbynRob winderAleksandra filipovicDeric shermanDrug administrationMemorial sloan kettering cancer centerPuretech healthTech healthFast trackFounded entity gallopFounded entitiesPrivate securities litigation reform actAnnual report

FDA Grants Fast Track Designation to LYT-200 in Recurrent/Metastatic HNSCC

FDA Grants Fast Track Designation to LYT-200 in Recurrent/Metastatic HNSCC
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New yorkUnited statesMemorial sloan kettering cancer centerDeric shermanAleksandra filipovicPuretech healthInternational prognostic scoring systemOncology congressandTech health

FDA Grants Fast Track Designation to LYT-200 in Head and Neck Cancers

The FDA’s fast track designation of LYT-200 in this population is supported by an ongoing phase 1/2 clinical trial.

United statesMemorial sloan kettering cancer centerNew yorkDeric shermanAleksandra filipovicPuretech health

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