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Benitec Biopharma
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U.S.A
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3940 Trust Way Hayward, CA. 94545
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+61 (0)3 8692-7222

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Details:

BB-301 is a novel, modified AAV9 capsid expressing a unique, single bifunctional construct promoting co-expression of both codon-optimized PABPN1 & two siRNAs against mutant PABPN1. It is being evaluated for the treatment of oculopharyngeal muscular dystrophy.


Lead Product(s): BB-301

Therapeutic Area: Rare Diseases and Disorders Product Name: BB-301

Highest Development Status: Phase I/ Phase IIProduct Type: Cell and Gene therapy

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable April 18, 2024

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The Company intends to use the net proceeds from the financing to fund the clinical development and related commercialization of BB-301, which is being evaluated in early-stage clinical trial studies for treating oculopharyngeal muscular dystrophy.


Lead Product(s): BB-301

Therapeutic Area: Rare Diseases and Disorders Product Name: BB-301

Highest Development Status: Phase I/ Phase IIProduct Type: Cell and Gene therapy

Partner/Sponsor/Collaborator: Citizens JMP

Deal Size: $40.0 million Upfront Cash: Undisclosed

Deal Type: Private Placement April 18, 2024

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Details:

BB-301 is a Cell and Gene therapy drug designed for Oculopharyngeal Muscular Dystrophy Related Dysphagia, utilizing the PABPN1 gene as a replacer and administered via intramuscular injection.


Lead Product(s): BB-301

Therapeutic Area: Rare Diseases and Disorders Product Name: BB-301

Highest Development Status: Phase I/ Phase IIProduct Type: Cell and Gene therapy

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable November 30, 2023

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Details:

The company intends to use the net proceeds to support the clinical development of BB-301, including the natural history lead-in study and the Phase 1b/2a BB-301 for the treatment of dysphagia associated with oculopharyngeal muscular dystrophy.


Lead Product(s): BB-301

Therapeutic Area: Rare Diseases and Disorders Product Name: BB-301

Highest Development Status: Phase IProduct Type: Cell and Gene therapy

Partner/Sponsor/Collaborator: JMP Securities

Deal Size: $30.0 million Upfront Cash: Undisclosed

Deal Type: Public Offering August 11, 2023

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Details:

The company intends to use the net proceeds to support the clinical development of BB-301, including the natural history lead-in study and the Phase 1b/2a BB-301 for the treatment of dysphagia associated with oculopharyngeal muscular dystrophy.


Lead Product(s): BB-301

Therapeutic Area: Rare Diseases and Disorders Product Name: BB-301

Highest Development Status: Phase I/ Phase IIProduct Type: Cell and Gene therapy

Partner/Sponsor/Collaborator: JMP Securities

Deal Size: $30.0 million Upfront Cash: Undisclosed

Deal Type: Public Offering August 08, 2023

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Details:

BB-301 is a novel, modified AAV9 capsid expressing bifunctional construct promoting co-expression of both codon-optimized Poly-A Binding Protein Nuclear-1 and two small inhibitory RNAs against mutant PABPN1 is currently in development for Oculopharyngeal Muscular Dystrophy.


Lead Product(s): BB-301

Therapeutic Area: Rare Diseases and Disorders Product Name: BB-301

Highest Development Status: IND EnablingProduct Type: Cell and Gene therapy

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable June 26, 2023

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Details:

BB-301 is currently in development for Oculopharyngeal Muscular Dystrophy. BB-301 results in robust inhibition of mutant PABPN1 and concomitant replacement of the codon-optimized PABPN1 protein. The treatment restores muscle strength and muscle weight.


Lead Product(s): BB-301

Therapeutic Area: Rare Diseases and Disorders Product Name: BB-301

Highest Development Status: Phase IProduct Type: Cell and Gene therapy

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable January 23, 2023

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Details:

The Company intends to use the net proceeds from this financing for the clinical development of BB-301, including the natural history lead-in study and the Phase 1b/2a BB301 treatment study.


Lead Product(s): BB-301

Therapeutic Area: Rare Diseases and Disorders Product Name: BB-301

Highest Development Status: IND EnablingProduct Type: Cell and Gene therapy

Partner/Sponsor/Collaborator: JMP Securities

Deal Size: $18.0 million Upfront Cash: Undisclosed

Deal Type: Public Offering September 16, 2022

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Details:

The company intends to use the proceeds for development of BB-301, including the natural history lead-in study and Phase 1b/2a BB-301 treatment study, for continued advancement of development activities, for general corporate purposes and for strategic growth opportunities.


Lead Product(s): BB-301

Therapeutic Area: Rare Diseases and Disorders Product Name: BB-301

Highest Development Status: IND EnablingProduct Type: Cell and Gene therapy

Partner/Sponsor/Collaborator: JMP Securities

Deal Size: $18.0 million Upfront Cash: Undisclosed

Deal Type: Public Offering September 12, 2022

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Details:

The BB-301 Tissue Transduction Study is the first of three studies to be conducted in large animals, with the overall goal of providing data to submit an investigational new drug application to the U.S. Food and Drug Administration, a mandatory step to conduct clinical trials.


Lead Product(s): BB-301

Therapeutic Area: Rare Diseases and Disorders Product Name: BB-301

Highest Development Status: IND EnablingProduct Type: Cell and Gene therapy

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable July 23, 2020

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