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BioWorld - Wednesday, April 15, 2026
Home » Keywords » AAV capsids

Items Tagged with 'AAV capsids'

ARTICLES

Illustration of green and yellow antibodies, DNA
Neurology/psychiatric

Vectory and Shape Therapeutics sign option and license agreement

Sep. 19, 2025
No Comments
Vectory Therapeutics BV and Shape Therapeutics Inc. have entered into an option and license agreement granting Vectory an exclusive option to evaluate Shape’s deep brain penetrating AAV capsid, SHP-DB1, for vectorized antibody payloads against three therapeutic targets.
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Concept art for adeno-associated viral-based gene therapy.

JCR’s third deal with Alexion gives rights to AAV capsids

July 15, 2025
By Marian (YoonJee) Chu
No Comments
Under a new licensing deal announced July 8, JCR Pharmaceuticals Co. Ltd. granted Alexion Pharmaceuticals Inc. rights to its adeno-associated virus (AAV) capsids for use in up to five of Alexion’s genomic medicines programs.
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Concept art for adeno-associated viral-based gene therapy.

JCR’s third deal with Alexion gives rights to AAV capsids

July 9, 2025
By Marian (YoonJee) Chu
No Comments
Under a new licensing deal announced July 8, JCR Pharmaceuticals Co. Ltd. granted Alexion Pharmaceuticals Inc. rights to its adeno-associated virus (AAV) capsids for use in up to five of Alexion’s genomic medicines programs.
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Illustration of brain in head highlighting the blood-brain barier.
Drug design, drug delivery & technologies

An adeno-associated virus to deliver therapeutic genes efficiently to the brain

May 20, 2025
No Comments

It is far easier and safer to inject drugs into veins than directly into the brain, yet it is extremely difficult for systemically delivered drugs to cross the blood-brain barrier and achieve therapeutic concentrations there.


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Neurology/psychiatric

Lilly licenses rights to use Sangamo’s neurotropic AAV capsid in genomic medicines

April 4, 2025
Sangamo Therapeutics Inc. has entered into a license agreement with Eli Lilly and Co., allowing Lilly to use Sangamo’s novel proprietary neurotropic AAV capsid, STAC-BBB, to deliver intravenously administered genomic medicines to treat certain diseases of the central nervous system.
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Ocular

Beacon Therapeutics to evaluate Abeona’s AAV204 capsid for ophthalmology indications

July 12, 2024
Abeona Therapeutics Inc. and Beacon Therapeutics Ltd. have signed an agreement for evaluation by Beacon of Abeona’s patented AAV204 capsid for the development and commercialization of potential gene therapies for select ophthalmology indications.
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Drug Design, Drug Delivery & Technologies

Sangamo reports primate data with neurotropic AAV capsid variant STAC-BBB

March 14, 2024
Sangamo Therapeutics Inc. has reported data from nonhuman primate (NHP) studies showing the potential of its proprietary AAV capsid variant, STAC-BBB, as a neurotropic capsid when administered intravenously at clinically relevant doses. STAC-BBB outperformed results for other evaluated neurotropic capsid variants.
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Art concept for gene therapy research
Drug Design, Drug Delivery & Technologies

Alexion, Astrazeneca Rare Disease agrees to acquire Pfizer’s preclinical rare disease gene therapy portfolio

July 31, 2023
Alexion, Astrazeneca Rare Disease, part of Astrazeneca plc, has entered a definitive purchase and license agreement for a portfolio of preclinical gene therapy programs and enabling technologies from Pfizer Inc.
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Neurology/Psychiatric

Prevail Therapeutics signs evaluation and option agreement for Sangamo’s AAV capsids

July 18, 2023
Sangamo Therapeutics Inc. has signed an evaluation and option agreement with Prevail Therapeutics Inc., a wholly owned subsidiary of Eli Lilly & Co., through which Prevail has been granted rights to evaluate certain proprietary adeno-associated virus (AAV) capsids developed by Sangamo and may exercise certain options to license these capsids for multiple undisclosed neurological targets.
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AAV 3D illustration

Voyager’s new AAV capsid approach draws Pfizer in $630M deal

Oct. 6, 2021
By Jennifer Boggs
Voyager Therapeutics Inc. is getting $30 million up front in a potential $630 million gene therapy deal with Pfizer Inc., the company’s first such agreement since a strategic refocusing effort earlier this year and a much-needed endorsement of a next-generation AAV capsid platform that has shown promising though early stage data.
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