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NANOBIOTIX Announces US FDA Protocol Acceptance for New Randomized Phase 2 Study Evaluating

PARIS and CAMBRIDGE, Mass., May 14, 2024 (GLOBE NEWSWIRE) NANOBIOTIX (Euronext: NANO –– NASDAQ: NBTX – the ‘‘Company’’), a late-clinical stage biotechnology company pioneering nanoparticle-based therapeutic approaches to expand

New yorkUnited statesFrance generalUnited kingdomLouis kayitalireJohnson enterprise innovation incDrug administrationUniversity of texas md anderson cancer centerGiven the companyStudy may proceed letterJanssen pharmaceuticaUnited states foodFast trackCancer centerEuronext parisNasdaq global select market

NANOBIOTIX Announces US FDA Protocol Acceptance for New Randomized Phase 2 Study Evaluating NBTXR3 for Patients with Stage Three Lung Cancer

NANOBIOTIX Announces US FDA Protocol Acceptance for New Randomized Phase 2 Study Evaluating NBTXR3 for Patients with Stage Three Lung Cancer
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United statesUnited kingdomFrance generalNew yorkLaurent wormserKevin gardnerBrandon owensLouis kayitalireGiven the companyCommunications departmentInvestor relations departmentDrug administrationUniversity of texas md anderson cancer centerJohnson enterprise innovation incStudy may proceed letterJanssen pharmaceutica

Monte Rosa Therapeutics Reports Third Quarter 2022 Financial Results and Business Updates

10.11.2022 - – Initiated Patient Dosing in Phase 1/2 Clinical Trial Evaluating MRT-2359, a GSPT1-directed Molecular Glue Degrader, for Treatment of MYC-driven Tumors – – Progressed VAV1 Molecular Glue Degrader Program into Lead Optimization – BOSTON, Nov. 10, .

New yorkUnited statesCity ofUnited kingdomComunidad autonoma de catalunaSan franciscoMonte rosaShai biranMarkus warmuthSereina rinikerPiper sandlerExchange commissionMonte rosa therapeutics incJp morgan health care conferenceDevelopment rd expensesDrug administration

C4 Therapeutics Reports Third Quarter 2022 Financial Results and Recent Business Highlights

C4 Therapeutics Reports Third Quarter 2022 Financial Results and Recent Business Highlights
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C4 Therapeutics Receives Study May Proceed Letter from U S FDA to Initiate Phase 1/2 Clinical Trial of CFT1946, an Orally Bioavailable BiDAC Degrader, in BRAF-V600 Mutant Solid Cancers

29.09.2022 - Phase 1/2 Clinical Trial Will Study CFT1946 in BRAF-V600 Mutant Solid Cancers Including Lung, Colorectal and Melanoma; Trial Initiation Expected by Year End 2022WATERTOWN, Mass., Sept. 29, 2022 (GLOBE NEWSWIRE) - C4 Therapeutics, Inc. (C4T) . Seite 1

Andrew hirschStudy may proceed letter