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BioWorld - Friday, December 5, 2025
Home » Authors » Cormac Sheridan

Articles by Cormac Sheridan

European Union flag, coins

European biotech sector tops $1.9B in Q2 equity funding

July 5, 2023
By Cormac Sheridan
European biotechnology firms engaged in the discovery and development of new therapeutics collectively raised $1.9 billion in equity funding during the second quarter (Q2) of the year. Despite the ongoing lack of an IPO market – particularly for European firms – the total is roughly comparable with historic norms, absent the pandemic-related boom years of 2020 and 2021. It represents the fourth highest total raised during the last six years.
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Cancer stem cells
Cancer

IPSirius targets cancer stem cells with iPSC-based vaccine

July 5, 2023
By Cormac Sheridan
IPSirius SAS, an early stage French immuno-oncology firm, hopes to obtain a clinical trial authorization from the U.K.’s Medicines and Healthcare Regulatory Products Agency next year, to enable it to move its novel therapeutic cancer vaccine into a first-in-human trial in patients with non-small-cell lung cancer.
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Mendus to evaluate vididencel-oral-aza combo as maintenance therapy in AML

June 27, 2023
By Cormac Sheridan
Later this year, Mendus AB plans to move its allogeneic cell-based cancer vaccine, vididencel, into a phase II combination trial with oral azacitidine to evaluate the regimen’s potential as a maintenance therapy in patients with acute myeloid leukemia (AML).
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Cancer stem cells
Newco news

IPSirius targets cancer stem cells with iPSC-based vaccine

June 23, 2023
By Cormac Sheridan
IPSirius SAS, an early stage French immuno-oncology firm, hopes to obtain a clinical trial authorization from the U.K.’s Medicines and Healthcare Regulatory Products Agency next year, to enable it to move its novel therapeutic cancer vaccine into a first-in-human trial in patients with non-small-cell lung cancer.
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Stock chart with falling red arrow

Uniqure stock drops 40% as Huntington’s disease data fail to convince

June 21, 2023
By Cormac Sheridan
Shares in Uniqure NV fell sharply on inconclusive interim data from a U.S. phase I/II trial of its gene therapy for Huntington’s disease. The stock (NASDAQ:QURE) hit a six-year low during trading on June 21, ending the day at $11.62, down 40%.
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Hemorrhagic stroke concept art
Newco news

Bioxodes turning tick’s trick into stroke drug

June 19, 2023
By Cormac Sheridan
Could a bioactive peptide secreted in the saliva of ticks offer a useful therapy for people who have experienced intracerebral hemorrhage (ICH)? That’s the question Bioxodes SA has set out to answer, and the company is about to move its first-in-class drug candidate, Ir-CPI, which has dual anti-thrombotic and anti-inflammatory effects, into a phase IIa trial in patients with ICH.
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Art concept for gene therapy research

Cash crunch looming for Sangamo

June 16, 2023
By Cormac Sheridan
After almost 30 years in business, Sangamo Therapeutics Inc. is finally nearing a BLA filing for one of its programs. But the company, wounded by the recent loss of alliances with Biogen Inc. and Novartis AG, is also running out of cash and investor interest – and it badly needs a new deal to stay afloat.
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Lungs

Vicore Pharma raises $46M to fund phase IIb trial in IPF

June 9, 2023
By Cormac Sheridan
Vicore Pharma Holding AB grossed about SEK500 million (US$46 million) in a directed share issue that will fund a phase IIb trial of its lead drug candidate, C-21, in idiopathic pulmonary fibrosis (IPF).
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Concept art for adeno-associated viral-based gene therapy.

Next-gen AAV developer Kate Therapeutics debuts with $51M series A plus Astellas license deal

June 8, 2023
By Cormac Sheridan
Gene therapy developer Kate Therapeutics Inc. (KateTx), which is developing next-generation adeno-associated virus (AAV) vectors that target skeletal and cardiac muscle, has unveiled $51 million series A round and a licensing deal with Astellas Pharma Inc.
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AAVantgarde Bio secures $65M series A round for large gene delivery in AAV vectors

June 6, 2023
By Cormac Sheridan
AAVantgarde Bio SrL raised €61 million (US$65 million) in series A funding to take forward two novel approaches to gene therapy that aim to overcome the packaging limits of adeno-associated virus (AAV) vectors. The company plans to move its lead program, in retinitis pigmentosa associated with Usher syndrome type 1b, into the clinic later this year. A second program, in Stargardt disease, is a couple of years behind it.
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