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Valneva : Confirms Clinical Trial and Regulatory Submission Timelines for its Inactivated COVID-19 Vaccine Candidate VLA2001 - Form 6-K

Valneva Confirms Clinical Trial and Regulatory Submission Timelines for its Inactivated COVID-19 Vaccine Candidate VLA2001 Saint Herblain , January 6, 2022 - Valneva SE , a. | January 10, 2022

United kingdomJoshua drummThomas lingelbachVp global communications european investor relationsEuropean commissionEuropean medicines agencyVaccine programDynavax technologies corporation nasdaqValneva confirms clinical trialRegulatory submission timelinesEuronext parisChief executiveofficerDynavax technologies corporationConfirms initiationRolling reviewProvides updates

Zymeworks Announces Expansion of Zanidatamab Pivotal Trial in Asia in Collaboration with BeiGene and Associated Milestone Payment

VANCOUVER, British Columbia (BUSINESS WIRE) Dec 9, 2021

United statesNew zealandUnited kingdomBritish columbiaSouth koreaZymework azymetricMary klemRyan derchoZymeworks incEuropean medicines agencyBeigene ltdBiologics license applicationSouth americaMiddle eastBreakthrough therapyFast track

Ultimovacs Receives Dual FDA Fast Track Designation for UV1 in Advanced Malignant Melanoma

Press release content from Globe Newswire. The AP news staff was not involved in its creation.

Mary ann changHans vassgFast trackRolling reviewBiologic licenseAccelerated approvalPriority reviewCarlos de sousaChief executive officerAnn changLifesci advisorsGlobe newswireUltimovacs asa

Ascentage Pharma s MDM2-p53 Inhibitor Alrizomadlin (APG-115) Granted Fast Track Designation by the US FDA for the Treatment of Relapsed/Refractory Unresectable or Metastatic Melanoma

Ascentage Pharma s MDM2-p53 Inhibitor Alrizomadlin (APG-115) Granted Fast Track Designation by the US FDA for the Treatment of Relapsed/Refractory Unresectable or Metastatic Melanoma
prnewswire.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from prnewswire.com Daily Mail and Mail on Sunday newspapers.

United statesHong kongWestern australiaDajun yangAscentage pharmaMajor nationalAmerican society of clinical oncologyDrug administrationMd anderson cancer centerDana farber cancer instituteAmerican cancer societyNational comprehensive cancer networkFast track designationOrphan drug designationsClinical oncologyAnnual meeting

EMA prüft Zulassung des Corona-Impfstoffs von Sanofi

EMA prüft Zulassung des Corona-Impfstoffs von Sanofi
faz.net - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from faz.net Daily Mail and Mail on Sunday newspapers.

Vakzin sinovacCompany developed gskFrench manufacturer sanofiDoses are neededRolling reviewThey willWhether theAre approvedRussian funds sputnikChinese vakzin sinovacஉருட்டுதல் விமர்சனம்அவர்கள் விருப்பம்