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A Look Ahead in Life Sciences: What We Are Tracking in Q2 2024 and Beyond | Goodwin

As the life sciences, medtech, and diagnostic industries continue to expand and grow increasingly complex, so does the legal, regulatory, and compliance landscape. To help companies and.

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Avidity Biosciences (RNA) Receives FDA Rare Pediatric Disease Designation for AOC 1044

Avidity Biosciences (RNA) Receives FDA Rare Pediatric Disease Designation for AOC 1044
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Steve hughesAvidity biosciences incEuropean medicines agencyDrug administrationAvidity biosciencesRare pediatric diseaseRare pediatric disease designationOrphan designationFast track designationOrphan drugFast trackPediatric disease priority review voucher

Day One Announces FDA Acceptance of NDA and Priority Review for Tovorafenib in Relapsed or Progressive Pediatric Low-Grade Glioma (pLGG)

Priority review granted with PDUFA target action date of April 30, 2024BRISBANE, Calif., Oct. 30, 2023 Day One Biopharmaceuticals , a clinical-stage biopharmaceutical company dedicated to.

United statesJeremy benderLaura cooperOncology consortiumHead of communicationsExchange commissionDrug administrationEuropean commissionCompany on linkedinOne biopharmaceuticalsNew drug applicationPrescription drug user fee actPediatric disease priority review voucherPacific pediatric neuro oncology consortiumResponse asessmentNeuro oncology high grade glioma

Can-Fite Enters Rare Genetic Disease Field Based on impactful findings of a Fondazione Telethon and Naples University Researcher showing Piclidenoson is efficacious in Treating Lowe Syndrome

Can-Fite Enters Rare Genetic Disease Field Based on impactful findings of a Fondazione Telethon and Naples University Researcher showing Piclidenoson is efficacious in Treating Lowe Syndrome
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United statesPnina fishmanMotti farbsteinFite biopharmaDepartment of molecular medicineProgram coordinator of the cell biologyFite biopharma ltdTelethon institute of geneticsEuropean unionEuropean medicines agencyUniversity of naples federicoDrug administrationCan fite signedFondazione telethonAntonella de matteisMolecular medicine

Can-Fite Enters Collaboration with Fondazione Telethon to Co-Develop Treatment for Lowe Syndrome

Can-Fite Enters Collaboration with Fondazione Telethon to Co-Develop Treatment for Lowe Syndrome
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United statesFite biopharmaPnina fishmanTelethon institute of geneticsDrug administrationEuropean medicines agencyRare dailyFondazione telethonLowe syndromeTelethon instituteAntonella de matteisCell biologyDisease mechanismsOrphan drugPediatric disease priority review voucherCan fite chairman pnina