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BioWorld - Wednesday, July 8, 2026
Home » Topics » Europe, BioWorld

Europe, BioWorld
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Cancer cells

Flindr’s $21.4M series A advances immune modulators

April 24, 2024
By Nuala Moran
Flindr Therapeutics BV has raised €20 million (US$21.4 million) in a series A round to advance small-molecule immune modulators aimed at targets it has identified in cancer patients who respond to existing immunotherapies.
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Stem cells

Vertex taps Treefrog’s stem cell tech for up to $780M

April 23, 2024
By Caroline Richards

Vertex Pharmaceuticals Inc. has tapped into Treefrog Therapeutics SA’s high-throughput stem cell manufacturing technology in a deal worth potentially up to $780 million to help it advance its type 1 diabetes programs, including phase I/II asset VX-880.


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Remsima SC

Samsung Bioepis, Celltrion make biosimilar inroads in Europe, US

April 23, 2024
By Marian (YoonJee) Chu
Samsung Bioepis Co. Ltd. and Celltrion Inc. are making headway in Europe and U.S. with respective follow-on biologic products, with Samsung Bioepis the latest to gain EMA approval for Pyzchiva, a Stelara (ustekinumab, Janssen Pharmaceuticals Inc.) biosimilar, on April 23.
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E3 ubiquitin-protein ligase RNF25
Newco news

Outrun emerges from stealth with $10M for E3 ligase inhibitors

April 18, 2024
By Nuala Moran
Newco Outrun Therapeutics Ltd. has raised $10 million in a seed round to develop small-molecule E3 ubiquitin ligase inhibitors that prevent programmed protein degradation. The lead program targeting an E3 ligase that tags a tumor suppressor protein for destruction will now advance to preclinical development.
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British pound symbol

Theolytics hauls in $23.7M for oncolytic virus drug THEO-260

April 17, 2024
By Nuala Moran
Oncolytic virus specialist Theolytics Ltd. has raised £19 million (US$23.7 million) in its latest financing round, as it prepares to start phase I development of the lead product, THEO-260, later this year.
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EMA workshop signals support for psychedelics

April 17, 2024
By Nuala Moran
“The development of psychedelic medicines should adhere to the current European regulatory framework, at both the pan-European and member state level. It is imperative that developers understand and thoroughly apply the regulatory guidance and requirements that are in place.” That was the somewhat discouraging opening statement at the stakeholder workshop convened by the EMA to discuss the development and therapeutic use of psychedelic substances to address unmet medical needs in the area of mental health.
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Essential gaining neuroblastoma candidate in Renaissance buy

April 9, 2024
By Nuala Moran
Essential Pharma Ltd. is paying up to £70 million (US$88.7 million) to acquire Renaissance Pharma Ltd., taking ownership of Hu14.18, a treatment for high-risk neuroblastoma. The antibody has completed a 64-patient phase II trial conducted by St Jude’s Children’s Research Hospital, in which it showed an improvement in overall survival of around 50% compared to currently available therapies.
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Golden dollar coins

Medicxi, Starpharma create Petalion with $25M round

April 9, 2024
By Tamra Sami
A day after investing $40 million in China’s D3 Bio Inc., London-based venture capital firm Medicxi is investing $25 million to co-found a new U.K.-based company called Petalion Therapeutics Ltd. that will focus on an early stage oncology asset from Australia’s Starpharma Holdings Ltd. to develop novel dendrimer-based treatments.
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Business, data, dollars illustration

VC firm Medicxi invests $40M in China’s D3 Bio

April 8, 2024
By Nuala Moran
Medicxi has made its first ever investment in China – and its biggest single commitment to date – putting $40 million into D3 Bio Inc. The investment by the London-based venture capital firm will accelerate development of D3’s lead program D3S-001, a second generation KRAS G12C inhibitor, which is in phase II development in advanced solid tumors.
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Industry seeks clarity on EU’s joint clinical assessment plan

April 5, 2024
By Nuala Moran
With nine months to go before their introduction, the industry is flagging many uncertainties around the proposed guidelines for implementing joint clinical assessments.
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