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BioWorld - Saturday, March 28, 2026
Home » Topics » Europe, BioWorld

Europe, BioWorld
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New EMA measures aimed at reducing use of animals in drug development

Sep. 30, 2021
The EMA is taking another step in its efforts to reduce animal testing in drug development.
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U.K. flag on stethoscope

ABPI: Use lessons from COVID-19 to revitalize UK clinical trial research

Sep. 29, 2021
By Nuala Moran
LONDON – Industry-sponsored clinical research in the U.K. took a big hit in the pandemic and is still struggling to catch up – and to capitalize on innovative trial designs and delivery approaches that were so successful in speeding up COVID-19 studies.
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Emma-Walmsley-CEO-Glaxosmithkline-hero-pic-6-23

Activist investor Bluebell is latest to call for ‘sleeping’ GSK’s CEO to quit

Sep. 23, 2021
By Richard Staines
A second activist investor has questioned the leadership of Glaxosmithkline plc’s CEO Emma Walmsley, after Bluebell Capital Partners Ltd. took a reported £10 million (US$13.7 million) stake in the embattled U.K. pharma.
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Jeito extends global reach in oversubscribed $625M venture fund

Sep. 20, 2021
By Nuala Moran
LONDON – There were well-deserved celebrations in Paris on Sept. 20, as Jeito Capital toasted the oversubscribed close of its first fund at €534 million (US$625.5 million). This is claimed as the largest European venture fund dedicated to life sciences, exceeding the original target of €500 million, and with €340 million of the total raised under the constraints of the pandemic from January 2020 onward.
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Coronavirus data illustration

Researchers unveil algorithm to identify COVID-19 patients at high risk despite vaccination

Sep. 17, 2021
By Nuala Moran
LONDON – Researchers in the U.K. have applied the heft of national population-level databases to devise a new algorithm that predicts those people who are most at risk of hospitalization and death from COVID-19, despite having received two doses of vaccine.
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EU flag, syringe, capsules

Citing safety worries, EU regulators reject Pfizer’s tanezumab for osteoarthritis pain

Sep. 17, 2021
By Richard Staines
European regulators have rejected Pfizer Inc.’s tanezumab, casting further doubts on whether the FDA will okay the troubled drug that is intended as a non-opioid alternative for osteoarthritis pain.
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Booster rollout set to start in UK for COVID-19 mRNA vaccines

Sep. 14, 2021
By Nuala Moran
LONDON – The U.K. government has accepted the recommendation of medical experts and will begin the rollout of COVID-19 boosters from next week, using mRNA vaccines only. That follows data from the U.K. Cov-Boost trial, looking at combinations of initial and booster doses. The results showed Pfizer Inc./Biontech SE’s and Moderna Inc.’s products generated the best immune responses, regardless of which vaccine was administered initially.
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Health professional touching screen, digital/medical icons

Sensyne launches broader access to its EHR database

Sep. 13, 2021
By Nuala Moran
LONDON – Health data specialist Sensyne Health plc is opening up broader access to its U.S./U.K. patient information system with the launch of a subscription service giving accredited users the ability to interrogate more than 2 million longitudinal electronic health records. At an annual cost of £25,000 (US$34,602) per head, the company will provide “industrial scale” access to anonymized hospital records “to the smallest company or to a single researcher working in academe,” through the new Sensight service, said Paul Drayson, CEO.
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Valneva shares crater as UK cancels order for 100M COVID-19 shots

Sep. 13, 2021
By Richard Staines
Shares in France’s vaccine specialist Valneva SA were sharply down after the U.K. government tore up a contract to supply 100 million doses of its COVID-19 vaccine, codenamed VLA-2001. Until today, Valneva was one of the largest COVID-19 vaccine contractors with the U.K. government, which got its orders early in the pandemic. Valneva was supposed to be supplying 100 million doses of its inactivated virus vaccine to the U.K., which had an option on a further 90 million shots.
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U.K. flag and capsules

UK’s drugs regulator sets pace with drug approvals, but faces post-Brexit job cuts

Sep. 10, 2021
By Richard Staines
It was a busy week for the U.K.’s drugs regulator, the Medicines and Healthcare Products Regulatory Authority (MHRA), which fast tracked decisions on novel drugs for cancer and eczema and made a ruling on booster COVID-19 jabs from Astrazeneca plc and Pfizer Inc. But even as Prime Minister Boris Johnson tweeted his support over the approval of Amgen Inc.’s cancer drug Lumykras, there are questions over the future of the regulator as it faces a round of job cuts because of a lack of funding following Brexit.
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