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Can-Fite to Share its Rare Genetic Disease Lowe Syndrome Novel Treatment with Orphan Drug Japanese Companies

Can-Fite BioPharma Ltd. , a biotechnology company advancing a pipeline of proprietary small molecule drugs that address oncology, inflammatory and liver diseases, today announced that the.

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Can-Fite to Share its Rare Genetic Disease Lowe Syndrome Novel Treatment with Orphan Drug Japanese Companies - Can Fite Biofarma (AMEX:CANF)

Can-Fite BioPharma Ltd. (NYSE:CANF) (TASE: CANF), a biotechnology company advancing a pipeline of proprietary small molecule drugs that address oncology, inflammatory and liver diseases, today announced that the

Sari fishmanBusiness development drBusiness development at canDrug administrationFite biopharma ltdCan fite biopharmaBusiness developmentOrphan drugsBiojapan conferenceFondazione telethonAntonella de matteisDermatology can fiteLowe syndromeOrphan drug designationFast track designation

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