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BioWorld - Monday, April 27, 2026
Home » Authors » Cormac Sheridan

Articles by Cormac Sheridan

European Union map and coronavirus

EMA activates COVID-19 pandemic task force to galvanize European regulatory response

April 9, 2020
By Cormac Sheridan
DUBLIN – The EMA has activated a COVID-19 task force to coordinate and accelerate the European regulatory response to the pandemic. The task force is intended to take a lead role in shaping the development, authorization and post-approval surveillance of drugs and vaccines for treating or preventing COVID-19 infection.
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Immunomedics stock soars as efficacy signal prompts early halt of phase III TNBC trial

April 6, 2020
By Cormac Sheridan
DUBLIN – Immunomedics Inc. is stopping the phase III Ascent trial of its antibody-drug conjugate, sacituzumab govitecan, in triple-negative breast cancer (TNBC) on the unanimous recommendation of the study’s independent data safety monitoring committee, after a scheduled look at the study data uncovered what the company called “compelling efficacy.”
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Symphogen exterior

Servier acquiring immuno-oncology partner Symphogen

April 3, 2020
By Cormac Sheridan
DUBLIN – Les Laboratoires Servier SAS has thrown its partner Symphogen A/S a lifeline by agreeing to a takeover deal in which the Danish firm will become Servier’s center of excellence for antibody development.
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Lung cancer illustration

Another COVID-19 casualty: Ose shutters phase III Tedopi trial in NSCLC despite positive interim analysis

April 2, 2020
By Cormac Sheridan
DUBLIN – Ose Immunotherapeutics SA finds itself in the difficult place of hitting the primary endpoint of the first part of a phase III trial of Tedopi, a therapeutic vaccine, in non-small-cell lung cancer (NSCLC) while having to terminate the study without completing the crucial second part.
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Lungs, COVID-19 test tube, health care worker in PPE

Just breathe: Ethris, Neurimmune developing inhaled mRNA-encoded COVID-19 antibodies

April 1, 2020
By Cormac Sheridan
DUBLIN – Ethris GmbH and Neurimmune AG have formed a collaboration to develop nebulized, mRNA-encoded monoclonal antibodies directed at SARS-CoV-2, which will be delivered directly to the lungs of patients with COVID-19.
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Rino Rappuoli, chief scientist, GSK Vaccines

Vaccines vet Rappuoli backs trusted technology in race to combat COVID-19

March 31, 2020
By Cormac Sheridan
DUBLIN – Three different vaccine technologies are being deployed in the desperate global effort to combat the SARS-CoV-2 virus, but Rino Rappuoli, chief scientist at the GSK Vaccines arm of Glaxosmithkline plc, said he sees traditional protein-based adjuvanted subunit vaccines, the trusted workhorse of infectious disease prevention, as offering the best bet for delivering a safe and effective vaccine at scale, within the tight timescales necessitated by the present crisis. 
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Gold wireframe handshake

Sitryx banks $60M in immunometabolism drug deal with Lilly

March 31, 2020
By Cormac Sheridan
DUBLIN – Without particularly looking for a deal, immunometabolism specialist Sitryx Ltd. landed quite a large one – a licensing agreement in autoimmune disease with Eli Lilly and Co. involving up to four preclinical programs, for which it is receiving $50 million up front, $10 million as equity investment and up to $820 million in development milestones.
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Rino Rappuoli, chief scientist, GSK Vaccines

Vaccines vet Rappuoli backs trusted technology in race to combat COVID-19

March 30, 2020
By Cormac Sheridan
DUBLIN – Three different vaccine technologies are being deployed in the desperate global effort to combat the SARS-CoV-2 virus, but Rino Rappuoli, chief scientist at the GSK Vaccines arm of Glaxosmithkline plc, said he sees traditional protein-based adjuvanted subunit vaccines, the trusted workhorse of infectious disease prevention, as offering the best bet for delivering a safe and effective vaccine at scale, within the tight timescales necessitated by the present crisis. 
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Zolgensma product packaging

CHMP nods through multiple applications during virtual March meeting

March 27, 2020
By Cormac Sheridan
DUBLIN – Novartis AG, Bristol Myers Squibb Co. and Sanofi SA were among firms that secured positive opinions from EMA’s Committee for Medicinal Products for Human Use (CHMP) on marketing authorization applications for new therapies, which will progress to formal approvals 67 days from now. Because of the COVID-19 pandemic, the committee’s March meeting was held virtually.
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Microbiome illustration
Bio-Europe 2020

Seventure leads think-in on microbiome dealmaking

March 26, 2020
By Cormac Sheridan
DUBLIN – Bio-Europe Spring’s virtual panel on the partnering dynamic between big pharma and microbiome-focused biotech firms was essentially an in-house webinar hosted by Seventure Partners, a Paris-based venture capital fund that has led the way in investing in microbiome-related therapeutics, diagnostics and other products.
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