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BioWorld - Sunday, December 21, 2025
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Flag of China and masks

Policy advocates propose measures for clinical disruptions in China

March 20, 2020
By Elise Mak and Cornelia Zou
BEIJING – China was the first country to face serious disruptions in clinical trials caused by COVID-19, and policy advocates in the country moved quickly to identify lessons for future outbreaks and address the concerns of a biotech industry in dismay.
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T cells

Go toward the light: Soligenix CTCL therapy no FLASH in the pan

March 19, 2020
By Randy Osborne
Princeton, N.J.-based Soligenix Inc.’s quick response testing SGX-301 (synthetic hypericin) – with results shown after just six weeks of treatment – puts the company in strong position against cutaneous T-cell lymphoma (CTCL) as it readies for a “robust” discussion with the FDA.
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European Union flag, coins

EU boosts funding for COVID-19 epidemic, encourages clinical trial cooperation

March 19, 2020
By Nuala Moran
LONDON – As the epicenter of the COVID-19 epidemic shifted to Europe and the number of deaths in Italy exceeded the toll in China, the EU stepped up efforts to mount a coordinated response, with a big boost for collaborative R&D funding and a call for clinical research to be pooled in multicenter, multi-arm randomized controlled trials.
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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.
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Testing, testing

First repurposing trial for COVID-19 falls flat

March 19, 2020
By Anette Breindl
The first attempt at using existing drugs to treat patients infected with SARS-CoV-2 has yielded disappointing results. In 200 hospitalized patients with severe COVID-19, a 14-day regimen of twice-daily treatment with Kaletra/Aluvia (lopinavir/ritonavir, Abbvie Inc.) did not hasten recovery when added to the standard of care.
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Health professional recording info from patient

Delays and interruptions: Coronavirus taking a toll on clinical trials

March 18, 2020
By Nuala Moran
LONDON – In the rush to test drugs against COVID-19, clinical trials in other indications are starting to be interrupted by the strains on health care systems and the fact that many potential patients are those most at risk from the effects of the novel coronavirus.
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FDA, drug developers grapple with COVID-19's impact on trials

March 18, 2020
By Michael Fitzhugh
With medical researchers across the globe adjusting to the far-reaching impacts of COVID-19, commercial and academic trialists are taking action to protect essential studies. Regulators, too, are now joining the effort in a more concerted way, with the FDA issuing new guidance for industry, investigators and institutional review boards on conducting clinical trials during the pandemic.
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Antiviral favipiravir effective against COVID-19, China says

March 18, 2020
By Michael Fitzhugh
Randomized trials of the broad-spectrum antiviral favipiravir, marketed as an anti-influenza treatment by Fujifilm Holdings Corp., have shown "obvious efficacy" against COVID-19, according to Zhang Xinmin, head of the China National Center for Biotechnology Development.
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Fallopian tubes, ovaries and uterus

Calcium deposit: Obseva banks on UF data with GnRH therapy linzagolix

March 18, 2020
By Randy Osborne
Geneva-based Obseva SA’s phase III Primrose 2 trial with gonadotropin-releasing hormone (GnRH) antagonist linzagolix in heavy menstrual bleeding (HMB) due to uterine fibroids (UFs) hit the primary endpoint in 94% of patients, and the company in the second quarter of 2020 will report six-month data from the Primrose 1 study, which is also a phase III experiment, in the same indication.
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Coronavirus headlines

Verily uses COVID-19 to expand Project Baseline, aims to quell rampant privacy concerns

March 18, 2020
By Stacy Lawrence
Google sister company Verily Life Sciences LLC has been under an unprecedented amount of scrutiny since it was promoted over the weekend by President Donald Trump as responsible for a nationwide information and testing program for the emerging novel coronavirus.
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