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BioWorld - Saturday, January 31, 2026
Home » Newsletters » BioWorld

BioWorld

Dec. 30, 2020

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Coronavirus mutation illustration

COVID anniversary coincides with advent of more transmissible variants

It has been a year since Wuhan health authorities first issued a bulletin about a cluster of pneumonia cases of unknown cause, first bringing what would become the COVID-19 pandemic to the attention of the World Health Organization. Now, a mutation that significantly increases SARS-CoV-2’s transmissibility has been detected in the U.S. On Dec. 29, Colorado public health authorities reported the first known case of infection with the SARS-CoV-2 VUI 202012/01 (Variant Under Investigation, year 2020, month 12, variant 01), also called B.1.1.7, variant in the U.S. The patient in question, a male in his 20s, has not traveled internationally, indicating that the variant is already circulating more widely in the U.S. Read More
Astrazeneca-COVID-19-vaccine-vials

U.K. approves Astrazeneca/Oxford vaccine

LONDON – The COVID-19 vaccine developed by Astrazeneca plc and Oxford University has been approved by the U.K regulator, with the first doses being shipped on Dec. 30 and a mass vaccination program due to begin on Jan. 4. AZD-1222, now named COVID-19 Vaccine Astrazeneca, is authorized for emergency use and will require two doses for durable effect. Read More
Woman steadying hand tremor

High on Upneeq, up a creek with arbaclofen; new spasticity trial for Osmotica after second CRL?

Osmotica Pharmaceuticals plc’s amendment earlier this month to the NDA for arbaclofen in spasticity resulting from multiple sclerosis wasn’t enough to quell the concerns of the FDA, which smacked the firm with its second complete response letter (CRL). Read More

Regeneron presses on with its phase III COVID-19 monoclonal antibody study

Results of a futility analysis prompted Regeneron Pharmaceuticals Inc. to continue the phase III study of its virus-neutralizing monoclonal antibodies, a REGN-10933 and REGN-10987 cocktail for treating hospitalized COVID-19 patients who are seronegative and need low-flow oxygen. Read More
Vaccination

China's CNBG/Sinopharm COVID-19 vaccine is 79% effective

HONG KONG – China National Biotec Group (CNBG) said that BBIBP-CorV, one of the two COVID-19 vaccines it currently has under development, provides 79.34% protection against the coronavirus. Volunteers who received the vaccine in the phase III experiment produced high-tier antibodies, with a neutralizing antibody positive conversion rate of 99.52% after two doses, the company said. Read More

Second U.S. court blocks MFN rule

The latest global regulatory news, changes and updates affecting biopharma. Read More

Financings for Dec. 30, 2020

Biopharmas raising money in public or private financings, including: Oragenics. Read More

In the clinic for Dec. 30, 2020

Clinical updates, including trial initiations, enrollment status and data readouts and publications: Altimmune, Chiesi, Codiak, Emergent, Hepion, Lipocine, Neurorx, Nicox, Protalix, Regeneron, Sinopharm. Read More

Other news to note for Dec. 30, 2020

Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Arcturus, Moderna, Propanc, Vaxil, Vistagen, Wize. Read More

Regulatory actions for Dec. 30, 2020

Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Astrazeneca, Biocure, Chi-Med, Lygenesis, Osmotica, Pharos Vaccine, Tetra, Tracon. Read More

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