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BioWorld - Wednesday, December 17, 2025
Home » Authors » Nuala Moran

Nuala Moran

Articles

ARTICLES

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Immuno-oncology

Laigo raises €11.5M seed money for targeted protein degradation

Dec. 5, 2025
By Nuala Moran
No Comments
Laigo Bio BV has raised €11.5 million (US$13.7 million) in a seed round for the further development of a new approach to inducing targeted protein degradation by E3 ubiquitin ligases.
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Illustration of chromosome unraveling down to the DNA
Drug design, drug delivery & technologies

First phase of synthetic human genome project successfully completes

Dec. 5, 2025
By Nuala Moran
No Comments
The first phase of the U.K. synthetic human genome project has successfully completed, realizing key steps in chromosome synthesis. The work has demonstrated a multistep method for transfecting mouse stem cells with native human chromosomes, where they are stably maintained and can be manipulated to replace native DNA with synthetic DNA. The engineered chromosomes can then be transferred into a human cell in place of the native chromosomes.
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Newco news

Laigo raises €11.5M seed money for targeted protein degradation

Dec. 4, 2025
By Nuala Moran
No Comments
Laigo Bio BV has raised €11.5 million (US$13.7 million) in a seed round for the further development of a new approach to inducing targeted protein degradation by E3 ubiquitin ligases.
Read More
Stethoscope on UK flag

UK decline in commercial clinical trials continues

Dec. 3, 2025
By Nuala Moran
No Comments
Despite a raft of government policies to turn the ship around, the latest figures show a further decline in setting up and staging commercial clinical trials in the U.K., with a 25% fall in the number of patients recruited over the past two years.
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Flags of US and UK on negotiation table

UK/US deal fixes import tariff on drugs at 0% for next 3 years

Dec. 2, 2025
By Nuala Moran
No Comments
The U.K. government has secured a deal guaranteeing there will be no tariffs on the £6.6 billion (US$8.7 billion) of pharmaceutical products exported annually to the U.S., as part of a package of measures under which the U.K. will pay more for patented drugs.
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Elderly woman holding illustration of brain with missing puzzle piece

Vandria’s phase I data offer new mode of action in Alzheimer’s

Dec. 2, 2025
By Nuala Moran
No Comments
Vandria SA published phase I data on a potential new mechanism of action in treating Alzheimer’s disease, demonstrating its orally available and brain-penetrant mitochondria-boosting compound, VNA-318, engages its intended target.
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Scientist holding semaglutide pill

Novo’s semaglutide fails in phase III Alzheimer’s trials

Nov. 24, 2025
By Nuala Moran
No Comments
Novo Nordisk A/S’ wild card bet that its GLP-1 receptor agonist semaglutide could be used to treat Alzheimer’s disease has not paid off, with the company reporting two phase III trials have shown no effect on slowing disease progression.
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Female doctor and patient
FT Global Pharma and Biotech Summit

Could restricting diversity efforts stall women’s health research?

Nov. 21, 2025
By Nuala Moran
No Comments
Recent progress in redressing the historical underfunding and neglect of women’s health could be undermined by the backlash against diversity, equity and inclusion (DEI) initiatives, according to executives participating in the FT Global Pharma and Biotech Summit 2025 in London Nov. 11-12.
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Flag of Scotland against blue sky

Scotland sets out 10-year plan to double its life sciences sector

Nov. 21, 2025
By Nuala Moran
No Comments
The Scottish government has published a strategy setting out a roadmap to more than double the size of Scotland’s life sciences sector over the next 10 years. The most recent data show the sector currently contributes £10.5 billion (US$13.8 billion) in turnover to the economy, supporting 46,000 jobs. The aim of the strategy is to increase this to £25 billion by 2035.
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Probiotics, bacteria on white background
Gastrointestinal

UK study reveals inconsistencies in global microbiome research

Nov. 21, 2025
By Nuala Moran
No Comments
The U.K. Medicines and Healthcare products Regulatory Agency is calling for unified standards to harmonize microbiome research, after revealing major inconsistencies in the results when labs around the world analyzed identical reference samples of gut bacteria.
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