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Bavarian Nordic A/S: Bavarian Nordic Submits Supplemental BLA Seeking U S FDA Approval of Freeze-Dried Formulation of Smallpox and Mpox Vaccine

Bavarian Nordic A/S: Bavarian Nordic Submits Supplemental BLA Seeking U S FDA Approval of Freeze-Dried Formulation of Smallpox and Mpox Vaccine
finanznachrichten.de - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from finanznachrichten.de Daily Mail and Mail on Sunday newspapers.

United kingdomPaul chaplinGraham morrellUs biomedical advanced researchCompany announcementDevelopment authorityOffice of theDrug administrationBiomedical advanced researchBiologics license applicationChief executive officerModified vaccinia ankara bavarian nordicBavarian nordicAssistant secretaryVice president investor relationsPaddock circle advisors

Bavarian Nordic Seeks FDA Approval For Freeze-Dried Smallpox, Monkeypox Vaccine; Stock Up

Bavarian Nordic Seeks FDA Approval For Freeze-Dried Smallpox, Monkeypox Vaccine; Stock Up
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Drug administrationBavarian nordicBiologics license application

FDA Extends Review Period for Dupilumab in COPD With Type 2 Inflammation

FDA Extends Review Period for Dupilumab in COPD With Type 2 Inflammation
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Drug administrationBiologics license applicationPrescription drug user fee act

Glancy Prongay & Murray LLP Reminds Investors of Looming Deadline in the Class Action Lawsuit Against Checkpoint Therapeutics, Inc (CKPT)

Glancy Prongay & Murray LLP Reminds Investors of Looming Deadline in the Class Action Lawsuit Against Checkpoint Therapeutics, Inc (CKPT)
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United statesLos angelesCharles linehanCharlesh linehanGlancy prongay murrayCheckpoint therapeutics incDrug administrationGlancy prongayCheckpoint therapeuticsBiologics license applicationClass periodPark eastAttorney advertising

First results from late-breaking Phase 3 PALOMA-3 study show five-fold reduction in infusion-related reactions with five-minute subcutaneous amivantamab administration

First results from late-breaking Phase 3 PALOMA-3 study show five-fold reduction in infusion-related reactions with five-minute subcutaneous amivantamab administration
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United statesNatashab leighlPrnewswire johnsonJanssen biotech incNone of janssen research developmentAmerican society of clinical oncology annual meetingEuropean medicines agencyAmerican lung associationNational cancer instituteWorld health organizationAmerican cancer societyAmerican society of clinical oncologyJanssen research developmentNational comprehensive cancer network incExchange commissionPrincess margaret cancer centre