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INOVIO Receives FDA Feedback that Data from Completed Phase 1/2 Trial of INO-3107 Can Be Used to Submit a BLA under Accelerated Approval Program

PLYMOUTH MEETING - INOVIO , a biotechnology company focused on developing and commercializing DNA medicines to help treat and protect people from HPV-related diseases, cancer, and infectious.

United statesJacqueline sheaKim mcclellanJennie willsonTriological societyRecurrent respiratory papillomatosis foundationAmerican laryngological associationDrug administrationEsophageal associationExchange commissionEuropean commissionBreakthrough therapy designationChief executive officerBroncho esophageal associationLaryngological associationAnnual meeting

Inovio Pharma (INO) Receives FDA Feedback that Data from Completed Phase 1/2 Trial of INO-3107

Inovio Pharma (INO) Receives FDA Feedback that Data from Completed Phase 1/2 Trial of INO-3107
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United statesJacqueline sheaKim mcclellanDrug administrationAmerican laryngological associationEsophageal associationTriological societyRecurrent respiratory papillomatosis foundationBreakthrough therapy designationChief executive officerAmerican broncho esophageal associationEuropean laryngological associationAnnual meetingLabel study

INOVIO Receives FDA Feedback that Data from Completed Phase 1/2 Trial of INO-3107 Can Be Used to Submit a BLA Under Accelerated Approval Program

INOVIO Receives FDA Feedback that Data from Completed Phase 1/2 Trial of INO-3107 Can Be Used to Submit a BLA Under Accelerated Approval Program
streetinsider.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from streetinsider.com Daily Mail and Mail on Sunday newspapers.

United statesJennie willsonJacqueline sheaKim mcclellanThomas hongAmerican laryngological associationExchange commissionPharmaceuticals incEuropean commissionRecurrent respiratory papillomatosis foundationTriological societyDrug administrationEsophageal associationBiological license applicationRecurrent respiratory papillomatosisBreakthrough therapy designation

Inovio Pharma (INO) Granted FDA Breakthrough Therapy Designation Granted for INO-3107

Inovio Pharma (INO) Granted FDA Breakthrough Therapy Designation Granted for INO-3107
streetinsider.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from streetinsider.com Daily Mail and Mail on Sunday newspapers.

United statesKim mcclellanJacqueline sheaDrug administrationEsophageal associationClinical research organizationTriological societyRecurrent respiratory papillomatosis foundationEuropean commissionAmerican laryngological associationBreakthrough therapyRecurrent respiratory papillomatosisChief executive officerOrphan drugAmerican broncho esophageal associationEuropean laryngological association

Precigen Announces FDA Confirmation that the Ongoing Phase 1/2 Study of PRGN-2012 AdenoVerse Immunotherapy Will Serve as the Pivotal Study to Support Accelerated Approval

– FDA confirmed that the ongoing Phase 1/2 single arm study will serve as pivotal and no additional randomized, placebo-controlled trial will be required to support submission of a.

Stevenm harasymClintt allenScott norbergPrecigen adenoverseKim mcclellanNational institutes of healthPrnewswire precigen incRecurrent respiratory papillomatosis foundationExchange commissionImmunotherapy clinical programPrecigen incDrug administrationComplete responseTherapy designationOrphan drug designationNational institutes