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The net proceeds will be used for the development of ABBV-RGX-314, being developed as a novel, one-time treatment for wet AMD that includes the NAV® AAV8 vector containing a gene encoding for a monoclonal anti-VEGF antibody fragment.


Lead Product(s): RGX-314

Therapeutic Area: Ophthalmology Product Name: ABBV-RGX-314

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

Partner/Sponsor/Collaborator: Morgan Stanley

Deal Size: $125.0 million Upfront Cash: Undisclosed

Deal Type: Public Offering March 06, 2024

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RGX-202 is a recombinant AAV8 containing a transgene encoding a novel microdystrophin, which is being evaluate for the treatment of duchenne muscular dystrophy.


Lead Product(s): RGX-202

Therapeutic Area: Genetic Disease Product Name: RGX-202

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 March 05, 2024

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RGX-121 is an investigational, one-time gene therapy designed to deliver the IDS gene that encodes the iduronate-2-sulfatase enzyme (I2S) using the NAV® AAV9 vector. It is under development for the treatment of Hunter syndrome.


Lead Product(s): RGX-121

Therapeutic Area: Genetic Disease Product Name: RGX-121

Highest Development Status: Phase II/ Phase IIIProduct Type: Cell and Gene therapy

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable February 07, 2024

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RGX-202 is a recombinant AAV8 containing a transgene encoding a novel microdystrophin. It is being developed for the treatment of duchenne muscular dystrophy in patients with ages 4 to 11 years old.


Lead Product(s): RGX-202

Therapeutic Area: Genetic Disease Product Name: RGX-202

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 February 07, 2024

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ABBV-RGX-314 consists of the NAV® AAV8 vector, which encodes an antibody fragment designed to inhibit VEGF. It is believed to inhibit the VEGF pathway. It is under phase 2 clinical development or the treatment of wet AMD.


Lead Product(s): RGX-314

Therapeutic Area: Ophthalmology Product Name: ABBV-RGX-314

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

Partner/Sponsor/Collaborator: AbbVie Inc

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable January 16, 2024

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RGX-202 is a Cell and Gene therapy drug infused intravenously for the treatment of Duchenne Muscular Dystrophy, transferring the micro-dystrophin gene.


Lead Product(s): RGX-202

Therapeutic Area: Genetic Disease Product Name: RGX-202

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 29, 2023

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Company will donate licenses to NAV® AAV8 and NAV® AAV9 from its NAV® Technology Platform to enable AMP® BGTC's development of these programs aimed at addressing ultra rare diseases i.e. Mucopolysaccharidosis type IVA (MPS IVA), also known as Morquio syndrome.


Lead Product(s): Undisclosed

Therapeutic Area: Rare Diseases and Disorders Product Name: Undisclosed

Highest Development Status: PreclinicalProduct Type: Cell and Gene therapy

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable May 15, 2023

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RGX-202 delivers a transgene for a novel microdystrophin that includes the functional elements of the C-Terminal domain found in naturally occurring dystrophin, leading to improved muscle resistance to contraction-induced muscle damage in dystrophic patients.


Lead Product(s): RGX-202

Therapeutic Area: Genetic Disease Product Name: RGX-202

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 11, 2023

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RGX-111 is designed to use the AAV9 vector to deliver the alpha-l-iduronidase gene to the CNS, which provides a permanent source of secreted IDUA beyond the blood-brain barrier, potentially preventing the progression of cognitive deficits in MPS I patients.


Lead Product(s): RGX-111

Therapeutic Area: Genetic Disease Product Name: RGX-111

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 February 24, 2023

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RGX-121 is designed to use the AAV9 vector to deliver the human iduronate-2-sulfatase gene which encodes the iduronate-2-sulfatase (I2S) enzyme to the CNS, allowing for long-term cross correction of cells throughout the CNS.


Lead Product(s): RGX-121

Therapeutic Area: Genetic Disease Product Name: RGX-121

Highest Development Status: Phase II/ Phase IIIProduct Type: Cell and Gene therapy

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable February 22, 2023

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