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FDA delays decision on Sanofi and Regeneron s Dupixent for COPD

FDA delays decision on Sanofi and Regeneron s Dupixent for COPD
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United statesRegeneron dupixentLen schleiferVerona pharmaceuticalsCommittee for medicinal products human useMedicinal productsHuman use

RYBREVANT®▼ (amivantamab) plus lazertinib shows longer

RYBREVANT®▼ (amivantamab) plus lazertinib shows longer
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Region flamandeSoult ukpyolsiSouth koreaUnited statesRepublic of koreaByoung chul choHenar heviaCraig tendlerAmerican lung associationSlate developmentJanssen cilag internationalAmerican society of clinical oncologyEuropean medicines agency seeking approvalJanssen cilag international nv incCommittee for medicinal products human useNational cancer institute

EMA Panel Nods to Seven New Cancer Drugs

EMA Panel Nods to Seven New Cancer Drugs
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Pomalidomide krkaPomalidomide zentivaEuropean medicines agencyCommittee for medicinal products human useEuropean unionPharmaceuticals deutschland gmbMedicinal productsHuman useDeutschland gmbhPomalidomide accordAccord healthcare

Severe Hypoglycemia in Diabetes Drug Approved in Europe

Severe Hypoglycemia in Diabetes Drug Approved in Europe
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Zealand pharmaEuropean commissionEuropean medicines agencyCommittee for medicinal products human useMedicinal productsHuman use

Calliditas Therapeutics: Calliditas partner STADA receives positive CHMP opinion recommending full approval for Kinpeygo® for the treatment of IgA nephropathy

Calliditas Therapeutics: Calliditas partner STADA receives positive CHMP opinion recommending full approval for Kinpeygo® for the treatment of IgA nephropathy
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United statesUnited kingdomRenee aguiar lucanderCommittee for medicinal products human useEuropean medicines agencyEuropean unionEuropean commissionExchange commissionNasdaq stockholmMedicinal productsHuman useAmerican depositary sharesNasdaq global select marketVisit calliditasPrivate securities litigation reform actIhr portfolio