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BioWorld - Thursday, April 16, 2026
Home » Topics » Regions » Europe

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Trimtech Therapeutics’ team

UK firm Trimtech emerges with $31M seed round for TRIM21 bispecifics

March 5, 2025
By Karen Carey
Trimtech Therapeutics closed a £25 million (US$31 million) oversubscribed seed funding round to advance its targeted protein degradation treatments for neurodegenerative and inflammatory diseases.
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Back pain

Persica’s PP-353 wins in back pain, advances to phase III

March 5, 2025
By Nuala Moran
Persica Pharmaceuticals Ltd. has delivered positive 12-month follow-up data from its phase Ib study of PP-353, an injectable antibiotic for treating chronic lower back pain, and is now looking for a partner and further financing to take the product into phase III development.
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Targeted cancer cell

Chimerix brings a rare cancer drug to the $935M Jazz party

March 5, 2025
By Lee Landenberger
Jazz Pharmaceuticals plc is buying Chimerix Inc. for $8.55 a share in cash, bringing the deal in at about $935 million. Jazz expands its cancer pipeline with the new acquisition’s lead candidate, dordaviprone, a small molecule for treating a rare, aggressive glioma that’s often found in children and young adults.
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White Euro symbol on blue background

Sofinnova raises €1.2B to invest in med tech, biotech, digital health

March 5, 2025
By Shani Alexander
Sofinnova Partners raised a whopping €1.2 billion (US$1.26 billion) over the past year to invest in life sciences companies ranging from incubation to later-stage growth, and spanning biotech, med tech, industrial biotech and digital medicine.
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Group of kids, faces huddled together
Genetic/congenital

UK releases three decades of children’s genomic data

March 5, 2025
By Nuala Moran
The U.K. has released a huge repository of children’s genomic data after sequencing blood samples from three large cohorts recruited at birth and followed across three decades. The power of the data is amplified by the large volume of longitudinal health information, biological samples and responses to surveys and questionnaires that has been provided by participating families. Before this, large-scale publicly available genome sequences were limited to adult cohorts, and the only childhood genome sequence data was from children with rare diseases.
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Group of kids, faces huddled together

UK releases three decades of children’s genomic data

March 4, 2025
By Nuala Moran
The U.K. has released a huge repository of children’s genomic data after sequencing blood samples from three large cohorts recruited at birth and followed across three decades. The power of the data is amplified by the large volume of longitudinal health information, biological samples and responses to surveys and questionnaires that has been provided by participating families.
Read More
White Euro symbol on blue background

Sofinnova raises €1.2B to invest in med tech, biotech, digital health

March 4, 2025
By Shani Alexander
Sofinnova Partners raised a whopping €1.2 billion (US$1.26 billion) over the past year to invest in life sciences companies ranging from incubation to later-stage growth, and spanning biotech, med tech, industrial biotech and digital medicine.
Read More
Blue peptide illustration

Abbvie enters $2.2B deal for Gubra’s amylin obesity drug

March 3, 2025
By Nuala Moran
Abbvie Inc. is buying into the obesity fray in a potential $1.875 billion development and commercialization agreement with Danish peptide drug discovery specialist Gubra A/S. In addition, there will be a $350 million up-front payment as Abbvie takes over the reins of GUB-014295 (referred to as Gubamy), a long-acting analog of the satiety hormone amylin, currently in phase I development.
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A DNA double helix rests on a print-out illustration of the DNA  base pair letters A, T, C and G.
Genetic/congenital

UK research effort finds 141 new rare disease-gene associations

March 3, 2025
By Nuala Moran
Whole genome sequencing has substantially accelerated the pace of discovery of genes that cause rare diseases, but while this has brought the diagnostic odyssey of some patients to a conclusion, 50% to 80% remain undiagnosed after initial analysis.
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Leqembi gets another thumbs-up amid CHMP February recommendations

Feb. 28, 2025
By Nuala Moran
The EMA’s Committee for Medicinal products for Human Use (CHMP) is standing by its opinion on Leqembi (lecanemab) after the European .mission pushed back against a recommendation in November 2024 that the Alzheimer’s disease drug be approved
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