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BioWorld - Tuesday, December 9, 2025
Home » Topics » Drugs » Gene therapy

Gene therapy
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Sarepta, Roche in $1.15B deal for DMD drug outside the U.S.

Dec. 23, 2019
By Lee Landenberger

Hui-Gene closes $14M series A to advance safe gene editing for rare diseases

Dec. 18, 2019
By Elise Mak
BEIJING – Gene therapy startup Hui-Gene Therapeutics Ltd. Co., of Shanghai, said it secured more than ¥100 million (US$14 million) in a series A financing round to develop a safer gene therapy to treat genetic diseases caused by single-base mutations.
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DNA illustration

Asuragen to develop CDx for Huntington’s disease gene therapies

Nov. 25, 2019
By Meg Bryant
Huntington’s disease is a fatal hereditary disease that results in the progressive breakdown of nerve cells in the brain. It erodes a person’s physical and mental abilities, usually beginning in their 30s and 40s, and to date has no cure. Now Austin-based Asuragen Inc. is joining forces with Wave Life Sciences USA Inc., of Cambridge, Mass., to develop companion diagnostics (CDx) for Wave’s investigative allele-selective therapeutic programs targeting the genetic cause of the disease.
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Gene therapy offers potential but poses logistical challenges

Oct. 14, 2019
By Brian Orelli
The mantra for a while has been that it's not good enough to get your drug approved, you've got to get it payed for, too. For gene therapy treatments, the payment is more complex, and you can add manufacturing and supply chain logistics to the list of challenges.
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Keeping the doctor away: Orchard gene therapy bid promising in MPS-I, more

Sep. 10, 2019
By Randy Osborne
As Wall Street ponders how pricing and reimbursement for gene therapies might shake out, companies in the field march intrepidly on, among them Orchard Therapeutics Inc., which early this month rolled out heartening results from an ongoing proof-of-concept trial evaluating the safety and efficacy of OTL-203 for mucopolysaccharidosis type I (MPS-I), a space that's heating up.
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Gyroscope closes $61M series B round for dry AMD gene therapy

Sep. 4, 2019
By Cormac Sheridan
DUBLIN – Gyroscope Therapeutics Ltd. raised £50.4 million (US$60.5 million) to further development of GT-005, its clinical-stage gene therapy for treating dry age-related macular degeneration (AMD), and to advance a second-generation of the subretinal delivery system it gained through its recent merger with Orbit Biomedical Ltd.
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S. Korea must ease regs, fast-track tech solutions to spur cell, gene therapy R&D

Sep. 3, 2019
By Jihyun Kim
SEOUL – South Korea's investors have become very interested in the global cell and gene therapy market. Licensing and M&A deals in the field have been active – a good sign for Korean biopharma firms eager to tap in.
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Ireland looking to play catch-up in cell, gene therapies manufacturing

July 31, 2019
By Cormac Sheridan
DUBLIN – Every technology shift has its winners and losers. Ireland, long a key location for small-molecule and biologics manufacturing, is now gearing up to ensure it is on the right side of the divide as the rollout of cell and gene therapies (CAGT) gathers momentum. There are no guarantees that the same technological and economic factors that contributed to its success during earlier eras of pharmaceutical and biopharmaceutical manufacturing will apply to the coming era of regenerative medicine. But the country's inward investment agency, IDA Ireland, is betting that its long-established relationships with the top tier of biopharma companies and its longstanding expertise in meeting FDA manufacturing requirements will help in the battle to win new investment projects.
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As gene therapy gains ground, Israel's Anchiano looks for success in bladder cancer

July 15, 2019
By Alfred Romann
TEL AVIV, Israel – With shares now listed in the U.S. and data from a pivotal trial for its key bladder cancer therapy coming soon, Anchiano Therapeutics Ltd. is poised to ride the wave of interest in gene therapy.
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More cell, gene, tissue-based therapies coming: ARM urges EU to tackle barriers to access

July 8, 2019
By Nuala Moran
LONDON – With five expensive advanced therapies recently approved in Europe and a further five expected to get approval in the near term, it is vital the hurdles that delay and preclude access – and which have led to the commercial failure of earlier products – are removed.
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