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BioWorld - Thursday, April 23, 2026
Home » Authors » Cormac Sheridan

Cormac Sheridan

Articles

ARTICLES

Lungs, COVID-19 test tube, health care worker in PPE

Could GSK reject benefit COVID-19 patients?

March 3, 2020
By Cormac Sheridan
DUBLIN – Could a recombinant human protein drug rejected by Glaxosmithkline plc in 2019 benefit patients with COVID-19 infection? Apeiron Biologics AG disclosed Wednesday Feb. 26 that an investigator-initiated pilot study of APN-01 is getting underway in Guangzhou, China.
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Life ring buoy floating in water

Redmile, Sofinnova back Redx turnaround with $34M equity, debt funding

March 2, 2020
By Cormac Sheridan
DUBLIN – Redx Pharma plc has put together a rescue package with two heavyweight investors that should ensure the company’s immediate future. Redmile Group LLC and Sofinnova Partners plan to provide up to £26.3 million (US$33.6 million) in funding to the struggling drug discovery and development firm.
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EU flag, pills, syringe

CHMP nixes Lilly bid to broaden Emgality label in migraine

Feb. 28, 2020
By Cormac Sheridan
DUBLIN – The EMA’s Committee for Medicinal Products for Human Use (CHMP) diverged from the FDA on a key decision at its monthly meeting, which concluded Feb. 28. It refused to back an application from Eli Lilly and Co. for a line extension to its migraine prevention drug, Emgality (galcanezumab), which would have authorized the drug for preventing attacks during an episode of cluster headaches.
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Lungs, COVID-19 test tube, health care worker in PPE

Could GSK reject benefit COVID-19 patients?

Feb. 26, 2020
By Cormac Sheridan
DUBLIN – Could a recombinant human protein drug rejected by Glaxosmithkline plc in 2019 benefit patients with COVID-19 infection? Apeiron Biologics AG disclosed Wednesday Feb. 26 that an investigator-initiated pilot study of APN-01 is getting underway in Guangzhou, China.
Read More

Shock away? Adrenomed’s adrecizumab hits phase II endpoint in septic shock

Feb. 26, 2020
By Cormac Sheridan
DUBLIN – Adrenomed AG disclosed Feb. 21 that its first-in-class antibody, adrecizumab, hit the primary safety and tolerability endpoint of a phase II trial in septic shock.
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Acute myeloid leukemia illustration

Advanced Biodesign advances toward the clinic with dual ALDH inhibitor

Feb. 25, 2020
By Cormac Sheridan
DUBLIN – Advanced Biodesign SAS secured €9 million (US$9.8 million) in new funding commitments to take its lead drug candidate, ABD-3001, into a phase I trial in acute myeloid leukemia (AML). The Lyon, France-based firm is investigating a novel drug mechanism associated with cancer cell metabolism, which could have application across several cancer types.
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Euro symbol in piggy bank

Aurora Science raises investment finance for early stage projects

Feb. 21, 2020
By Cormac Sheridan
DUBLIN – Meda AB’s acquisition in 2014 of the veteran Italian specialty pharma firm Rottapharm generated a €1.975 billion (US$2.2 billion) payday for the latter firm’s owners, the Rovati family. A small fraction of that amount is now being recycled into a new investment initiative, Aurora Science, which is a three-way partnership among Monza-based Rottapharm Biotech Srl (the R&D arm of the company that was not part of the Meda transaction), the Milan-based specialty pharma Italfarmaco SpA and Aurora-TT Srl, a Milan-based commercial technology transfer company.
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Cancer cell, dropper, test tubes

Immatics gets $50M up front in engineered T-cell therapy deal with GSK

Feb. 20, 2020
By Cormac Sheridan
DUBLIN – Immatics Biotechnologies GmbH is banking $50 million up front and could earn up to $550 million more in per-product milestones from an adoptive cell therapy deal in solid tumor indications with Glaxosmithkline plc, which initially involves two autologous cell therapies engineered to express T-cell receptors (TCRs) that bind novel cancer targets. Immatics would receive royalties on sales of any approved therapies.
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Neotx closes $45M C round for second coming of immuno-oncology agent

Feb. 19, 2020
By Cormac Sheridan
DUBLIN – Neotx Therapeutics Ltd. raised $45 million in a series C round to continue clinical development of an immuno-oncology agent that already has a long clinical history behind it. Its lead molecule, naptumomab estafenatox, is a fusion protein comprising an antibody fragment that recognizes the oncofetal antigen 5T4 and a bacterial “super-antigen” comprising a modified version of the Staphylococcal enterotoxin A.
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Capsule with Italian flag

Aurora Science raises investment finance for early stage projects

Feb. 18, 2020
By Cormac Sheridan
DUBLIN – Meda AB’s acquisition in 2014 of the veteran Italian specialty pharma firm Rottapharm generated a €1.975 billion (US$2.2 billion) payday for the latter firm’s owners, the Rovati family. A small fraction of that amount is now being recycled into a new investment initiative, Aurora Science, which is a three-way partnership among Monza-based Rottapharm Biotech Srl (the R&D arm of the company that was not part of the Meda transaction), the Milan-based specialty pharma Italfarmaco SpA and Aurora-TT Srl, a Milan-based commercial technology transfer company.
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