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Europe Approves Paroxysmal Nocturnal Hemoglobinuria Drug

The factor D inhibitor danicopan has been approved for use in Europe for patients with paroxysmal nocturnal hemoglobinuria with residual hemolytic anemia on standard therapy.

European unionEuropean medicines agencyEuropean commissionDrug administrationPriority medicinesMedicinal productsHuman useParoxysmal nocturnal hemoglobinuriaNh paroxysmal nocturnal hemoglobinuriaParoxysmal nocturnal haemoglobinuriaParoxysmal nocturnal hemoglobinuria pnhHemolytic anemia haemolytic anaemiaAnemia anaemiaBiologic therapyGenomics genomic medicineOrphan drugs

HOOKIPA Pharma to Host Investor Call on HB-200 and Planned

HOOKIPA announces alignment with FDA on pivotal trial design and protocol for HB-200 in combination with pembrolizumabHB-200 program receives Priority.

Joern aldagEuropean medicines agencyExchange commissionPharma incUs food drug administrationPriority medicinesDrug administrationHuman papillomavirusChief executive officerPrivate securities litigation reform actNasdaq hookHookipa pharma incSb 200Head and neck cancer

HOOKIPA Pharma to Host Investor Call on HB-200 and Planned Path to Registration

HOOKIPA Pharma to Host Investor Call on HB-200 and Planned Path to Registration
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Joern aldagMichael kaiserExchange commissionPharma incUs food drug administrationEuropean medicines agencyHost investor callPlanned pathPriority medicinesDrug administrationHuman papillomavirusChief executive officerPrivate securities litigation reform act

Vertex Pharma (VRTX) Advances Inaxaplin into Phase 3 Portion of Adaptive Phase 2/3 Trial

Vertex Pharma (VRTX) Advances Inaxaplin into Phase 3 Portion of Adaptive Phase 2/3 Trial
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Carmen bozicGlennm chertowData monitoring committeeStanford university school of medicineVertex pharmaceuticals incorporated nasdaqProgram steering committeeDrug administrationEuropean medicines agencyGlobal medicines developmentVertex pharmaceuticals incorporatedExecutive vice presidentMedical affairsChief medical officerStanford university schoolIndependent data monitoring committeeRare pediatric disease designation

Vertex Pharmaceuticals Incorporated: Vertex Advances Inaxaplin (VX-147) into Phase 3 Portion of Adaptive Phase 2/3 Clinical Trial for the Treatment of APOL1-Mediated Kidney Disease

Vertex Pharmaceuticals Incorporated: Vertex Advances Inaxaplin (VX-147) into Phase 3 Portion of Adaptive Phase 2/3 Clinical Trial for the Treatment of APOL1-Mediated Kidney Disease
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United statesCity ofUnited kingdomGlenn chertowHeather nicholsGlennm chertowMiroslava minkovaSusie lisaManisha paiCarmen bozicDennis riedlEuropean medicines agencyGlobal medicines developmentProgram steering committeeCompanies to workExchange commission