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Benitec Biopharma : Releases Third Quarter 2024 Financial Results and Provides Operational Update - Form 8-K

Benitec Biopharma : Releases Third Quarter 2024 Financial Results and Provides Operational Update - Form 8-K
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New south walesUnited statesKishen mehtaIrina kofflerExchange commissionBenitec biopharma incBenitec or companyLifesci advisorsSuvretta capital managementBenitec biopharma releases third quarterProvides operationalPositive interim clinical trial dataFirst oculopharyngeal muscular dystrophySubject dosedClinical treatment study reportedSafely dosed

Benitec Biopharma Releases Third Quarter 2024 Financial Results and Provides Operational Update

Benitec Biopharma Releases Third Quarter 2024 Financial Results and Provides Operational Update
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New south walesUnited statesIrina kofflerKishen mehtaExchange commissionBenitec or companyLifesci advisorsSuvretta capital managementBenitec biopharma incBiopharma releases third quarterProvides operationalPositive interim clinical trial dataFirst oculopharyngeal muscular dystrophySubject dosedClinical treatment study reportedSafely dosed

Benitec Biopharma Releases Third Quarter 2024 Financial Results And Provides Operational Update

Benitec Biopharma Releases Third Quarter 2024 Financial Results And Provides Operational Update
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New south walesKishen mehtaExchange commissionBenitec or companyBenitec biopharma incSuvretta capital managementPositive interim clinical trial dataFirst oculopharyngeal muscular dystrophySubject dosedClinical treatment study reportedSafely dosedAdditional interim clinical safety dataClinical efficacy dataSeveral study subjectsSecond halfHistory study

Benitec Biopharma (BNTC) Reports Positive Interim Clinical Trial Data for First OPMD Subject Treated with BB-301

Benitec Biopharma (BNTC) Reports Positive Interim Clinical Trial Data for First OPMD Subject Treated with BB-301
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New south walesUnited statesExchange commissionEuropean medicines agencyIrina kofflerlifesci advisorsBenitec or companyBenitec biopharma incDrug administrationCommittee for orphan medicinal productsBenitec biopharmaOculopharyngeal muscular dystrophyOrphan drugOrphan medicinal productsExecutive chairmanChief executive officerNatural history

Benitec Biopharma Provides Overview of the BB-301 Phase 1b/2a Clinical Trial Design for 2022

Benitec Biopharma Provides Overview of the BB-301 Phase 1b/2a Clinical Trial Design for 2022
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United statesNew south walesJaya morakisPrnewswire benitec biopharma incNature communicationsBenitec biopharma incHearing researchOculopharyngeal muscular dystrophyWestern europeOpen label dose escalation studyClinical activityIntramuscular dosesMaximally effective doseStudy subject evaluationDynamic imaging swallowing toxicityPharyngeal area