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COVID-19 Scoop: Epoch-Making GoldenBiotech s Oral COVID-19 New Drug Trial Got Green Light from the FDA to Extend Recruiting Severe COVID-19 Patients | Taiwan News

COVID-19 Scoop: Epoch-Making GoldenBiotech s Oral COVID-19 New Drug Trial Got Green Light from the FDA to Extend Recruiting Severe COVID-19 Patients | Taiwan News
taiwannews.com.tw - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from taiwannews.com.tw Daily Mail and Mail on Sunday newspapers.

United statesUnited kingdomT ai peiSouth koreaSouth koreanAlex liuSanova pharmaSanova pharma gesmbHerba groupDrug administrationKorea co ltdData monitoring committeeGolden biotechnology corporationGolden biotechnology corpPrnewswire golden biotechnology corp tpexBiotechnology corp

Mobocertinib approved as first oral therapy for EGFR Exon20+ NSCLC

Mobocertinib approved as first oral therapy for EGFR Exon20+ NSCLC
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United statesAmerican society of clinical oncologyDrug administrationDana farber cancer instituteThermo fisher scientificOncomine dx target testBreakthrough therapy designationFast track designationOrphan drug designationAccelerated approvalClinical oncologyTorsades de pointesDana farber cancerஒன்றுபட்டது மாநிலங்களில்அமெரிக்கன் சமூகம் ஆஃப் மருத்துவ புற்றுநோயியல்டானா ஃபார்‌பர் புற்றுநோய் நிறுவனம்

COVID-19 Scoop: Epoch-Making GoldenBiotech s Oral COVID-19 New Drug Trial Got Green Light from the FDA to Extend Recruiting Severe COVID-19 Patients

COVID-19 Scoop: Epoch-Making GoldenBiotech s Oral COVID-19 New Drug Trial Got Green Light from the FDA to Extend Recruiting Severe COVID-19 Patients
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Takeda Pharmaceutical : EXKIVITY (mobocertinib) Approved by U S FDA as the First Oral Therapy Specifically Designed for Patients with EGFR Exon20 Insertion+ NSCLC

Takeda Pharmaceutical : EXKIVITY (mobocertinib) Approved by U S FDA as the First Oral Therapy Specifically Designed for Patients with EGFR Exon20 Insertion+ NSCLC
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United statesUnited kingdomTeresa bitettiMarcia hornRyoko matsumotoLauren padovanAmerican society of clinical oncologyOncology centerTakeda pharmaceutical company limitedWorld health organizationDrug administrationTakeda pharmaceutical companyExchange commissionInternational cancer advocacy networkDana farber cancer institutePharmaceutical company limited

BridgeBio Pharma Receives FDA Fast Track Designation for Investigational Therapy for the Treatment of Limb-girdle Muscular Dystrophy Type 2i (LGMD2i)

BridgeBio Pharma Receives FDA Fast Track Designation for Investigational Therapy for the Treatment of Limb-girdle Muscular Dystrophy Type 2i (LGMD2i)
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United statesBio pharmaDouglas sprouleKatherine yauDrug administrationBridgebio pharma incSecurities exchangeEuropean medicines agencyBio pharma incMl bio solutions incUnited states foodFast trackLimb girdle muscular dystrophy typeMolybdenum cofactor deficiencyOrphan drug designationEuropean medicines