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BioWorld - Friday, April 24, 2026
Home » Topics » Asia-Pacific » Japan

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Eye and DNA

Cellusion raises $9.5M to support ocular cell therapy

Jan. 12, 2022
By Gina Lee
Cellusion Inc. recently closed a ¥1.1 billion ($9.5 million) financing, bringing its total 2021 fundraising to ¥1.7 billion. The company is preparing to enter the clinic with CL-S001, its corneal endothelial substitute cell candidate for treating corneal edema due to endothelial dysfunction, or bullous keratopathy.
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Prism offers Genentech peptide mimetic small-molecules library for multitarget collaboration

Jan. 11, 2022
By Gina Lee
Prism Biolab Co. Ltd. has added Genentech Inc., a unit of Roche Holding AG, to the list of users for its peptide mimetic small-molecules library after signing a multitarget research collaboration and licensing agreement.
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Kyowa Kirin expands Inveniai AI platform collaboration once again

Jan. 11, 2022
By Gina Lee
Inveniai LLC and Kyowa Kirin Co. Ltd. have expanded their partnership a second time, inking their most recent multiple drug discovery agreement. The multiyear deal will see the duo discover novel targets and treatments for therapeutic areas across Kyowa Kirin’s portfolio and areas of interest using Inveniai’s artificial intelligence (AI) platform.
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Prism offers Genentech peptide mimetic small-molecules library for multitarget collaboration

Jan. 10, 2022
By Gina Lee
Prism Biolab Co. Ltd. has added Genentech Inc., a unit of Roche Holding AG, to the list of users for its peptide mimetic small-molecules library after signing a multitarget research collaboration and licensing agreement. Under the agreement, Tokyo-based Prism Biolab will open its Pepmetics Library, a library of peptide mimetic small molecules, to screen against targets selected by Roche and Genentech.
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Kyowa Kirin expands Inveniai AI platform collaboration once again

Jan. 10, 2022
By Gina Lee
Inveniai LLC and Kyowa Kirin Co. Ltd. have expanded their partnership a second time, inking their most recent multiple drug discovery agreement. The multiyear deal will see the duo discover novel targets and treatments for therapeutic areas across Kyowa Kirin’s portfolio and areas of interest using Inveniai’s artificial intelligence (AI) platform.
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Nec partners with Bostongene to bring tumor analysis tests to Japan

Dec. 21, 2021
By Gina Lee
Nec Corp. has inked a global partnership agreement with Bostongene Corp. that will bring the latter’s Bostongene Tumor Portrait Tests to Japanese patients. Japan is the first market outside of the U.S. for the tests, according to the companies.
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DNA in drug capsules, digital background

After safety troubles, Astellas signs $1.6B deal with Dyno Therapeutics to improve AAV tech

Dec. 7, 2021
By Richard Staines
Japan’s Astellas Pharma Inc. is continuing its investment in gene therapies, following up its $3 billion acquisition of Audentes Therapeutics Inc. with a technology licensing deal with Dyno Therapeutics Inc. potentially worth more than $1.6 billion. Central to the deal is Cambridge, Mass.-based Dyno’s adeno-associated virus (AAV) vector technology, which can be used to direct gene therapies to skeletal and cardiac muscle.
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DNA in drug capsules, digital background

After safety troubles, Astellas signs $1.6B deal with Dyno Therapeutics to improve AAV tech

Dec. 1, 2021
By Richard Staines
Japan’s Astellas Pharma Inc. is continuing its investment in gene therapies, following up its $3 billion acquisition of Audentes Therapeutics Inc. with a technology licensing deal with Dyno Therapeutics Inc. potentially worth more than $1.6 billion. Central to the deal is Cambridge, Mass.-based Dyno’s adeno-associated virus (AAV) vector technology, which can be used to direct gene therapies to skeletal and cardiac muscle.
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Cytomegalovirus in a human cell

A new first as FDA approves Takeda drug to treat CMV in transplant recipients

Nov. 30, 2021
By Michael Fitzhugh
Following an FDA priority review, Takeda Pharmaceutical Co. Ltd.'s oral antiviral, maribavir, has won U.S. approval as the first drug in the country to treat resistant cytomegalovirus (CMV) infection and disease in adult and pediatric transplant recipients. The drug will be marketed as Livtencity.
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A new first as FDA approves Takeda drug to treat CMV in transplant recipients

Nov. 24, 2021
By Michael Fitzhugh
Following an FDA priority review, Takeda Pharmaceutical Co. Ltd.'s oral antiviral, maribavir, has won U.S. approval as the first drug in the country to treat resistant cytomegalovirus (CMV) infection and disease in adult and pediatric transplant recipients. The drug will be marketed as Livtencity.
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