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BB

WKN: A3D3BP | ISIN: US08205P2092 | Ticker-Symbol:
NASDAQ
18.09.26 | 21:59
11,000 US-Dollar
0,00 % 0,000
Branche
Biotechnologie
Aktienmarkt
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1-Jahres-Chart
BENITEC BIOPHARMA INC Chart 1 Jahr
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BENITEC BIOPHARMA INC 5-Tage-Chart

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DiCitizens reiterates Benitec Biopharma stock rating ahead of FDA talks1
MoBenitec Biopharma Inc. - 10-K, Annual Report1
MoBenitec Biopharma Inc.: Benitec Biopharma Releases Full Year 2026 Financial Results and Provides Operational Update92All six Cohort 1 (low dose BB-301) patients have completed the full 12-month post-treatment follow-up period, and Cohort 2 (high dose BB-301) is fully enrolled with all three patients having been...
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MoBenitec GAAP EPS of -$0.98 in-line2
BENITEC BIOPHARMA Aktie jetzt für 0€ handeln
MoBenitec Biopharma Inc. - 8-K, Current Report3
18.05.Citizens reiterates Benitec BioPharma stock rating on dose data2
14.05.Benitec Biopharma Inc. - 10-Q, Quarterly Report2
14.05.Benitec Biopharma Inc. - 8-K, Current Report2
14.05.Benitec Biopharma Inc.: Benitec Biopharma Releases Third Quarter 2026 Financial Results and Provides Operational Update436Late-breaking abstract for BB-301 presented at the Muscular Dystrophy Association (MDA) Clinical and Scientific Conference in March demonstrated durable responses to low dose BB-301 at 12-months and...
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12.05.Evercore ISI initiates Benitec BioPharma stock coverage at outperform3
28.04.Benitec presents OPMD gene therapy data at May conference1
09.03.Benitec Biopharma Inc.: 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 Clinical & Scientific ...295- Oculopharyngeal Muscular Dystrophy (OPMD) Patients treated with low dose BB-301 and high dose BB-301 experienced significant improvements in throat closure, throat emptying, and total dysphagic...
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11.01.Benitec Biopharma Inc.: Benitec Biopharma Provides Positive Long-Term Clinical Study Results for BB-301 Phase 1b/2a Clinical Trial Demonstrating Robust Efficacy and Continued Durability of Response760• Patient 1 of Cohort 1 has now completed the 24-month follow-up timepoint, and at month-24 post-treatment Patient 1 continued to demonstrate the powerful disease-modifying effects of BB-301, with...
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14.11.25Benitec Biopharma Inc.: Benitec Biopharma Releases First Quarter 2026 Financial Results and Provides Operational Update367-Fast Track Designation was granted for BB-301 following U.S. Food and Drug Administration (FDA) review of positive interim clinical study results and proprietary Responder Analysis planned for use...
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03.11.25Benitec Biopharma Inc.: Benitec Biopharma Provides Positive Interim Clinical Study Results for BB-301 Phase 1b/2a Clinical Trial and Receives FDA Fast Track Designation for BB-301465Fast Track Designation was granted for BB-301 following FDA review of positive interim clinical study results and proprietary Responder Analysis planned for use in pivotal study for BB-301 BB-301...
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22.09.25Benitec Biopharma Inc.: Benitec Biopharma Releases Full Year 2025 Financial Results and Provides Operational Update190Interim Clinical Study Results for Cohort 1 of the BB-301 Phase 1b/2a Treatment Study Anticipated in Q4 2025 Enrollment of the First Subject into Cohort 2 of the BB-301 Phase 1b/2a Treatment Study...
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