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BioWorld - Saturday, February 14, 2026
Home » Authors » Cormac Sheridan

Articles by Cormac Sheridan

Truffle hunting: Truffle Capital closes 5th Biomedtech fund at $279M

Dec. 18, 2019
By Cormac Sheridan
DUBLIN – Truffle Capital closed off its fifth Biomedtech fund with a €250 million (US$279 million) raise, which it will deploy in about a dozen companies located mainly in France. The fund took a little longer to close than originally planned but it is significantly larger than it had originally intended. “Our initial objective was €200 million,” Truffle Capital CEO and co-founder Philippe Pouletty told BioWorld.
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Two positive CHMP opinions in December take 2019 tally to 41

Dec. 13, 2019
By Cormac Sheridan
DUBLIN – The European Medicines Agency’s Committee for Medicinal Products for Human Use closed out its year’s work with positive opinions on two applications, Novartis AG’s Beovu (brolucizumab) in wet age-related macular degeneration and Merck & Co. Inc.’s Recarbrio for treating gram negative infections in adults.
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Sunshine’s better on the other side

Numab banks $15M equity investment in 3Sbio immuno-oncology pact

Dec. 12, 2019
By Cormac Sheridan
DUBLIN – Numab Therapeutics AG is banking an equity investment of CHF15 million (US$15.2 million) from its latest Asian partner, Sunshine Guojian Pharmaceutical (Shanghai) Co. Ltd., as part of a broad alliance to develop up to five multispecific antibodies from three programs based on Numab’s Match platform.
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Immunos raises $15M for multitasking immune-activating agents

Dec. 10, 2019
By Cormac Sheridan
DUBLIN – Immunos Therapeutics AG raised CHF15 million (US$15.2 million) in a series A round to move a novel immuno-oncology platform designed to turn cold tumors hot into early clinical development.
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Sanofi swoops in on Synthorx with $2.5B bid

Dec. 9, 2019
By Cormac Sheridan
DUBLIN – Sanofi SA is paying a hefty 172% premium to acquire Synthorx Inc. for $68 per share, or $2.5 billion in all, to add a clinical-stage immuno-oncology asset to its pipeline and a platform technology that will enable it to optimize cytokine-based drugs for cancer and autoimmune disease.
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DNA illustration
Newco news

Dyno to scale the heights of AAV vector engineering

Dec. 6, 2019
By Cormac Sheridan
Startup firm Dyno Therapeutics Inc. is attempting to engineer a new generation of adeno-associated virus (AAV) capsids by navigating its way across what it calls the “capsid fitness landscape,” in order to optimize the key parameters that affect capsid performance: production, delivery efficiency, biodistribution, immunogenicity and thermostability.
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4Teen4 closes $8M A round to test first-in-class cardiogenic shock drug

Dec. 5, 2019
By Cormac Sheridan
DUBLIN – 4Teen4 Pharmaceuticals GmbH raised €6.9 million (US$7.7 million) in a series A round to take procizumab, a first-in-class inhibitor of circulating dipeptidyl-peptidase 3 (cDPP3), into clinical trials for patients with cardiogenic shock.
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Imcheck closes $53M B round for antibodies targeting gamma delta T cells

Dec. 4, 2019
By Cormac Sheridan
DUBLIN – Imcheck Therapeutics SAS raised €48 million (US$53.2 million) in a series B financing round to move a pipeline of antibodies targeting gamma delta T cells into the clinic.
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Novartis barrels into PCSK9 inhibitor market with $9.7B bid for The Medicines Co.

Nov. 25, 2019
By Cormac Sheridan
DUBLIN – Novartis AG is making a $9.7 billion bet that the economics of an siRNA-based drug can better those of monoclonal antibodies and thus provide it with a dominant position in a major but still emerging cardiovascular drug market. The Basel, Switzerland-based pharma made an $85 per share offer for The Medicines Co., which has taken inclisiran, an siRNA-based inhibitor of proprotein convertase subtilisin/kexin type 9 (PCSK9) to the brink of an approval in reducing the risk of a cardiovascular event – heart attack or stroke – in high-risk patients with cardiovascular disease or high levels of low-density lipoprotein cholesterol (LDL-C) who are inadequately controlled on current therapies.
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Promising but preliminary

Crispr Therapeutics’ interim data: First two patients functionally cured by CRISPR/Cas9 therapy?

Nov. 19, 2019
By Cormac Sheridan
DUBLIN – Crispr Therapeutics AG has delivered what appears, so far at least, to be a safe, functional cure for the first patient enrolled in each of its phase I/II trials of lead CRISPR/Cas9 gene editing therapy CTX-001, in beta-thalassemia and in sickle cell disease.
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