FDA
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Benitec Biopharma posts wider loss as BB-301 trial advances
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Seaport Therapeutics appoints Dr. Sharon Mates to board of directors
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Benitec Biopharma Announces Positive Interim Phase 1b/2a Results for High Dose BB-301 and Continued Durable Improvements for Low Dose BB-301 Treatment at the 2026 Muscular Dystrophy Association Clinic
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Benitec Biopharma Provides Positive Long-Term Clinical Study Results for BB-301 Phase 1b/2a Clinical Trial Demonstrating Robust Efficacy and Continued Durability of Response
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Benitec Biopharma Announces Appointment of Sharon Mates Ph.D. to its Board of Directors
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Benitec Biopharma Reports Positive Interim Clinical Results for Three Subjects Treated with BB-301 in Phase 1b/2a Study to be Presented at the 2025 Muscular Dystrophy Association Clinical & Scient
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Benitec Biopharma Releases Full Year 2024 Financial Results and Provides Operational Update
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