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European Commission Approves ADCETRIS® (brentuximab vedotin) for the Treatment of Adult Patients with Previously Untreated CD30+ Stage III Hodgkin Lymphoma in Combination with AVD

European Commission Approves ADCETRIS® (brentuximab vedotin) for the Treatment of Adult Patients with Previously Untreated CD30+ Stage III Hodgkin Lymphoma in Combination with AVD
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United statesJohn cunninghamJohn radfordAwny farajallahJun saitoInternational mediaInternational agency for research on cancerEuropean commissionExchange commissionAmerican cancer societyCommittee for medicinal products human useEuropean unionUniversity of manchesterTakeda pharmaceutical companyImportant safety information european unionHealth canada

Homeowners in Bell and Paramount Can Now Fund Renewable Energy and Water Saving Projects, Earthquake Resiliency, HVAC, Through PACE Financing

Homeowners in Bell and Paramount Can Now Fund Renewable Energy and Water Saving Projects, Earthquake Resiliency, HVAC, Through PACE Financing
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United statesLos angeles countyCity of bellVilma cuellar stallingsRobert gilesContactsevern williamsMonica arroyoProperty assessed clean energyFunding groupClean energy sectorDepartment of financing protectionInnovative formFinancing now availableHome run financingApproval basedHome equity

Takeda s EXKIVITY® (mobocertinib) Receives Approval from the NMPA of China, Becoming the First and Only Therapy Available for Patients with EGFR Exon20 Insertion+ NSCLC

Takeda s EXKIVITY® (mobocertinib) Receives Approval from the NMPA of China, Becoming the First and Only Therapy Available for Patients with EGFR Exon20 Insertion+ NSCLC
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United statesUnited kingdomSouth koreaNoord hollandGreat britainSean shanJun saitoLauren padovanAwny farajallahGlobal medical affairs oncologyTakeda pharmaceutical company limitedWorld health organizationTakeda pharmaceutical companyExchange commissionNational medical products administrationAmerican cancer society

FDA Approves Mirvetuximab Soravtansine for Ovarian Cancer

This is an accelerated approval for use in patients with folate receptor alpha–positive disease, identified by an assay that was approved alongside the drug.

Ursula matulonisDrug administrationDana farber cancer instituteApproval basedOvarian cancerAlignant ovarian neoplasmBiologic therapyAlignant neoplasiaPeritoneal cancerAncer of the peritoneumFallopian tubesUs food and drug administrationNited states food and drug administrationAntibody drug conjugates adcs

Stock Market | FinancialContent Business Page

Stock Market | FinancialContent Business Page
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United statesSharonm castellinoNational cancer instituteChildren oncology groupEmory university school of medicineHodgkin lymphoma disease committee chairDrug administrationSeagen incStage developmentExchange commissionEuropean unionDepartment of pediatricsApproval basedStudy that demonstratedDisease progressionSecond malignancy