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BioWorld - Tuesday, December 30, 2025
Home » Topics » Infection » Coronavirus

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Newco news

Covicept lands Forbion backing for mission to tackle RNA viruses

Feb. 5, 2021
By Michael Fitzhugh
Covicept Therapeutics Inc., a young San Diego-based company focused on developing a small molecule to inhibit the replication and spread of SARS-CoV-2 and other RNA viruses, has launched with $2.3 million in seed funding from European VC firm Forbion. The company, spun out of research at the University of California, San Diego, aims to initiate its first clinical study in the middle of 2021.
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Regulatory actions for Feb. 5, 2021

Feb. 5, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Actinogen, BMS, Celltrion, Innocare, J&J, Novavax, RDIF, TG.
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Other news to note for Feb. 5, 2021

Feb. 5, 2021
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Alphageneron, Curevac, Diamond, Hyloris, Multimmune, Onxeo, Pfizer, Purna .
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In the clinic for Feb. 5, 2021

Feb. 5, 2021
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Achilles, Astrazeneca, Covaxx, GSK, I-Mab, PTC, Sanofi, Spark, Spero.
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FDA icons

Regulatory attorney says warning letters likely to spike under new FDA administration

Feb. 4, 2021
By Mark McCarty
U.S. FDA warning letters have been a staple of regulatory life since the late 1990s, but James Boiani, a regulatory attorney with Epstein, Becker & Green P.C., said it’s no stretch of the imagination that warning letter volumes will jump in 2021. This is to some extent because the volume of warning letters dropped significantly over the past four years, and Boiani advised that all FDA-regulated industries will see more warning letters unless they are communicative with the agency about inspectional findings.
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Regulatory front for Feb. 4, 2021

Feb. 4, 2021
By Mark McCarty
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: CEO tells patients their deaths were impending for profit; DeGette, Bucshon ink new testing legislation; NICE: Acupath’s URO17 test needs more data.
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Regulatory actions for Feb. 4, 2021

Feb. 4, 2021
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: B-Secur, Claronav Kolahi, RapidAI, Precision Biomonitoring, Precision Spine.
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Other news to note for Feb. 4, 2021

Feb. 4, 2021
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: 23andme, Ambu, Coopercompanies, Curadel Surgical Innovations, Bioaffinity Technologies, Dxs, Emitbio, Essilorluxottica, Horizon Therapeutics, Illumina, Insightec, Medidata, Mnx Global Logistics, Mprobe, Neogenomics, Newronika, Oxford Immunotec, Parexel, Philips, Phillips-Medisize, Pieriandx, Quidel, RNA Disease Diagnostics, Sera Prognostics, Shanghai Fosun Long March Medical Science, Sightglass Vision, Stella Diagnostics, Subcuject, Tcg Lifesciences, Varian, Vuzix, Webops.
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BioWorld MedTech’s Diagnostics Extra for Feb. 4, 2021

Feb. 4, 2021
By Meg Bryant
Keeping you up to date on recent developments in diagnostics, including: A deep learning tool to predict cardiovascular risk; Smartphone-based COVID-19 test; PCOS passed on in the epigenes.
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Syringe, bottles of COVID-19 vaccine on U.K. map

U.K. launches mixed COVID-19 vaccine trial

Feb. 4, 2021
By Nuala Moran
LONDON – The U.K has started the world’s first trial alternating an adenoviral vectored COVID-19 vaccine with one that delivers the virus spike protein instructions encoded in messenger RNA. The heterologous prime boost trial will recruit 820 participants into an eight-arm study comparing different combinations of the Astrazeneca plc/Oxford University and Pfizer Inc./Biontech SE vaccines, administered in a different order and at different intervals.
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