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BioWorld - Monday, January 26, 2026
Home » Topics » Gene therapy, BioWorld

Gene therapy, BioWorld
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Gold chain link engraved with "partnership"

Novartis, Sarepta join Dyno’s enterprise to boldly go to new gene therapy frontier

May 11, 2020
By Cormac Sheridan
DUBLIN – Dyno Therapeutics Inc., an early stage gene therapy firm applying artificial intelligence to advanced capsid engineering, has entered partnerships with Novartis AG and Sarepta Therapeutics Inc., in ophthalmic indications and muscle diseases, respectively, which have over $2 billion in biobucks attached.
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RA Session II, CEO, Taysha Gene Therapies

Taysha Gene Therapies seeded with $30M, Avexis lineage

April 30, 2020
By Michael Fitzhugh
Taysha Gene Therapies Inc., a new Dallas-based company reuniting former executives of Avexis Inc. and its funders, has launched with a $30 million seed financing intended to advance a pipeline of 15 new AAV-based candidates. Its team expects to file four INDs by the end of 2021, starting with one for GM2-gangliosidosis that could move to the clinic later this year.
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DNA illustration

Sofinnova Partners backs Naldini-led gene therapy startup

April 20, 2020
By Cormac Sheridan
DUBLIN – Genespire Srl, a Milan-based startup led by gene therapy pioneer Luigi Naldini, is the third company to receive funding from Sofinnova Partners’ Italian €108 million (US$117.5 million) gene therapy fund, the Sofinnova Telethon Fund.
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Eye chart

Daiichi Sankyo makes strides in gene therapy development in joint project

April 17, 2020
By David Ho
HONG KONG – Daiichi Sankyo Co. Ltd., Mitsubishi UFJ Capital Co. Ltd. and Nagoya Institute of Technology have kicked off research on a joint project for a gene therapy that could be applied to the restoration of vision.
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Ireland’s Avectas raises $20M in a series C

April 16, 2020
By Lee Landenberger
Avectas Ltd., of Dublin, brought in a $20 million series C financing, ratcheting the total equity investment in the company to $40 million. Privately held Avectas, formed in 2012 as a spin-out from Ireland’s Maynooth University, said it plans to accelerate the clinical translation and commercial scale-up of its cell engineering technology and expand its staffing in Ireland.
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Silhouette with keyhole

Promising pipeline for disease-modifying therapies targeting Parkinson’s disease

April 14, 2020
By Peter Winter
It has been more than 200 years since British doctor James Parkinson first identified the symptoms of a condition that he termed shaking palsy; unfortunately, there is still no cure to the disease that carries his name.
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VIA Thaw system by Cytiva

Newly renamed Cytiva retains heart of GE Healthcare’s biopharma manufacturing unit

April 13, 2020
By Nuala Moran
LONDON – These are hardly times for a fanfare, but this month saw the unveiling of a new name in bioprocessing, following the formal closing of the $21.4 billion sale of GE Healthcare’s Life Sciences to Danaher Corp. The business, now renamed Cytiva, has turnover of $3.3 billion, nearly 7,000 employees and operations in 40 countries. More than 75% of FDA-approved biologic drugs use its products in their manufacture.
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Nucleotide’s in: Gene therapy high water lifts Affinia with $60M series A

April 1, 2020
By Randy Osborne
The allure of gene therapy was proved yet again as Waltham, Mass.-based Affinia Therapeutics Inc. bagged an oversubscribed $60 million series A financing to boost the push for drugs to benefit people affected by muscle and central nervous system conditions.
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DNA data illustration

Elevatebio ups the ante in cell, gene therapies with $170M series B

March 30, 2020
By Randy Osborne
Cambridge, Mass.-based Elevatebio LLC has triple-pronged plans for its $170 million series B round, which the company said will be directed toward manufacturing cell and gene therapies, enabling new technology platforms, and pursuing therapeutics.
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Ovarian cancer illustration

Ovarian fever pumps VBL shares, positive peek at phase III cancer gene therapy

March 26, 2020
By Randy Osborne
During the conference call on earnings in March, CEO Dror Harats told investors that “the most important thing” about VBL Therapeutics Ltd.’s then-upcoming analysis of interim phase III data with gene therapy VB-111 (ofranergene obadenovec) is that it was “designed in a way that will enable us to tell the market if we are at least as good as what we've seen” in the phase II experiment.
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