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BioWorld - Saturday, February 7, 2026
Home » Authors » Cormac Sheridan

Articles by Cormac Sheridan

Oncopeptides on track for Q2 NDA for melflufen in myeloma

March 26, 2020
By Cormac Sheridan
Oncopeptides AB remains on track for an NDA filing in the second quarter for its peptide-drug conjugate, melflufen, in relapsed refractory multiple myeloma (RRMM).
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siRNA bound to mRNA

Silence is golden: Astrazeneca buys into siRNA platform with $80M down payment

March 25, 2020
By Cormac Sheridan
DUBLIN – Silence Therapeutics plc entered a wide-ranging siRNA-based drug discovery and development deal with Astrazeneca plc that has propelled it toward the front ranks of siRNA platform companies. It is banking an up-front payment of $60 million, another $20 million as an equity investment and up to $400 million in option fees and milestone payments per candidate drug, in an alliance that could entail up to five active programs within three years.
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Actemra product packaging

Genentech moves Actemra into phase III COVID-19 trial

March 24, 2020
By Cormac Sheridan
DUBLIN – The Genentech arm of Roche Holding AG plans to move its interleukin-6 inhibitor, Actemra, into a global phase III trial in patients with severe pneumonia associated with COVID-19 infection.
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Microbiome illustration
Bio-Europe 2020

Seventure leads think-in on microbiome dealmaking

March 24, 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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Bio-Europe Spring 2020

Hunting for niches in cardiometabolic disease, as Secarna passes dyslipidemia milestone

March 23, 2020
By Cormac Sheridan
DUBLIN – For quite some time, cardiometabolic disease has been largely off the map for most small biotechs and for the venture capital investors that support them. Is that situation about to change? Maybe, maybe not was the mixed message arising from a Bio-Europe Spring 2020 virtual panel discussion on cardiometabolic disease.
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Lungs

FDA says yes to NO: Bellerophon Therapeutics wins expanded access approval for inhaled nitric oxide system

March 20, 2020
By Cormac Sheridan
DUBLIN—Can high-dose inhaled nitric oxide (NO) make a meaningful contribution to patients with COVID-19 infection? The FDA was sufficiently persuaded by the data presented by Bellerophon Therapeutics Inc. to grant it expanded access approval for its iNOpulse system for pulmonary delivery of NO.
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Actemra product packaging

Genentech moves Actemra into phase III COVID-19 trial

March 19, 2020
By Cormac Sheridan
DUBLIN – The Genentech arm of Basel, Switzerland-based Roche Holding AG plans to move its interleukin-6 (IL-6) inhibitor, Actemra (tocilizumab), into a global phase III trial in patients with severe pneumonia associated with COVID-19 infection.
Read More
Euro symbol in piggy bank

Oncoone closes $14M series A round for targeting MIF isoform

March 18, 2020
By Cormac Sheridan
DUBLIN – The middle of a pandemic may not be the optimal time to launch an oncology-focused company, but Klosterneuburg, Austria-based Oncoone Research & Development GmbH unveiled a €13 million (US$14.1 million) series A round Wednesday, March 18, and laid out plans to develop several different approaches to targeting an immunologically distinct form of a ubiquitous inflammatory cytokine, which is unique to cancer cells and which is associated with a poor prognosis.
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Hand holding dollar sign

Versant building out to drive returns

March 10, 2020
By Cormac Sheridan
DUBLIN – Versant Ventures was one of a handful of investors to profit from Passage Bio Inc.’s recent upsized IPO. The Philadelphia-based gene therapy firm planned to raise $125 million initially but eventually hauled in $216 million by issuing 12 million shares, which it priced at $18 per share on Feb. 27. The IPO price valued Versant’s holding at $89 million. As well as participating in the IPO – the actual amount involved has not been disclosed – it invested $35 million across three private rounds, between September 2018 and August 2019, according to SEC filings.
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Two-year data buoy Hansa’s imlifidase MAA as CHMP decision looms

March 9, 2020
By Cormac Sheridan
DUBLIN – Hansa Biopharma AB is nearing a key milestone in its evolution, as a regulatory decision on its first marketing authorization application (MAA) looms. The EMA’s Committee for Medicinal Products for Human Use (CHMP) is expected to deliver an opinion during the second quarter on its application for imlifidase in supporting kidney transplants in sensitized patients.
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