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Biodexa Enters Into Exclusive License to eRapa™, a Phase 3 Ready Asset for the Treatment of Familial Adenomatous Polyposis (FAP)

Biodexa Enters Into Exclusive License to eRapa™, a Phase 3 Ready Asset for the Treatment of Familial Adenomatous Polyposis (FAP)
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United statesUnited kingdomSan antonioUniversity of texasStephen dufilhoEmtora biosciencesRapamycin holdings incCompany american depositoryResearch institute of texasUniversity of texas health san antonioCancer prevention research institute of texasNational institutes of healthLadenburg thalmann coBiodexa pharmaceuticalsNational cancer instituteEnters into exclusive license

Biodexa Pharmaceuticals (BDRX) Enters Exclusive License to eRapa

Biodexa Pharmaceuticals (BDRX) Enters Exclusive License to eRapa
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United statesUnited kingdomUniversity of texasSan antonioStephen dufilhoEmtora biosciencesUniversity of texas health san antonioBiodexa pharmaceuticalsNational cancer instituteLadenburg thalmann coResearch institute of texasNational institutes of healthRapamycin holdings incCompany american depositoryCancer prevention research institute of texasEnters into exclusive license

Are Carbon Nanotubes Toxic?

This article explores carbon nanotube toxicity, emphasizing how purity, shape, size, and functionalization affect safety in nanomedicine.

Sumio iijimaBiosensors baselPriyom boseInternational journal of molecular sciencesCarbon nanotubeCarbon nanotubesGene deliveryNanoscale resFront bioengReactive oxygen speciesOutlining their roleBiological macromoleculesInternational journalMurine granuloma modelInstilled carbon nanotubesIntj mol

PANTHERx®Rare Selected by Edenbridge Pharmaceuticals as Specialty Pharmacy for Yargesa® (miglustat 100 mg capsules)

PITTSBURGH, April 1, 2024 /PRNewswire/ PANTHERx®Rare, a leader in rare disease product patient access and support services in the United States, is pleased to announce that it was selected

United statesRob snyderMohand gaucherPrnewswire pantherxRare disease centerUtilization review accreditation commissionNational human genome research instituteNational gaucher foundationAccreditation commission for health careEdenbridge pharmaceuticalsNational organization for rare disordersEdenbridge pharmaceuticalAccreditation commissionHealth careOrphan drugsChoice award

Eisai Completes Submission of LEQEMBI® (lecanemab-irmb) Supplemental Biologics License Application for IV Maintenance Dosing for the Treatment of Early Alzheimer s Disease to the U S FDA

/PRNewswire/ Eisai Co., Ltd. (Headquarters: Tokyo, CEO: Haruo Naito, "Eisai") and Biogen Inc. (Nasdaq: BIIB, Corporate headquarters: Cambridge,.

Hong kongUnited statesUnited kingdomSaudi arabiaSouth koreaGreat britainLibby holmanJack coxChuck trianoChristophera viehbacherHaruo naitoTsujim protofibrilsEisai incPrnewswire eisai co ltdExchange commissionEisai co ltd