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BioWorld - Saturday, May 2, 2026
Home » Topics » Infection » Coronavirus

Coronavirus
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DNA sequence and COVID-19 virus cells

Study finds variants that increase risk of severe COVID-19

March 7, 2022
By Nuala Moran
The world’s largest genomics study in patients with life-threatening COVID-19 infections has uncovered 16 new genetic variants associated with severe disease and drawn up a roadmap for research into new therapies and diagnostics. The research involved comparing the complete genome sequences of 7,491 patients admitted to 224 intensive care units in the U.K. against those of 48,400 participants in Genomics England’s 100,000 Genomes project, and of a further 1,630 people who had mild COVID-19. While some of the gene variants found in the Genomicc study affect the function of a protein, others influence the amount of the protein that is expressed. An example is mucin-1, where overexpression led to worse outcomes.
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Other news to note for March 7, 2022

March 7, 2022
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Breg, Calyx, Clinchoice, J2 Medical, Oncimmune, Premier, Tytocare.
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Regulatory actions for March 7, 2022

March 7, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Amgen, Aravax, Bharat Biotech, Biogen, Eisai, Merck, Nymox, Ocugen.
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In the clinic for March 7, 2022

March 7, 2022

Clinical updates, including trial initiations, enrollment status and data readouts and publications: American Cryostem, Aravive, Atreca, Coherus, Eli Lilly, Equillium, Evofem, Incyte, Mink, Recursion.


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Regulatory actions for March 4, 2022

March 4, 2022
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Circa Scientific, KSL Diagnostics, SQI Diagnostics.
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Person using COVID-19 antigen test at home

FDA clamping down on rapid antigen tests for COVID-19

March 3, 2022
By Mark McCarty
The FDA continues its tight surveillance of rapid antigen tests for the COVID-19 pandemic and has issued three safety communications advising against the use of these tests thus far in the month of March. In each instance, the test is made by the manufacturer of name, but was not authorized in the U.S., making these misbranded products despite their legal use in other nations.
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Clinical data illustration

With fewer pandemic updates, clinical data down by 11%

March 3, 2022
By Karen Carey
While clinical trial updates in 2022 started off slow, the gap with last year appears to be closing, even as pandemic activity diminishes.
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Pause in recruitment to REMAP CAP COVID-19 trial affects Dimerix’s lead candidate, DMX-200

March 3, 2022
By Tamra Sami
PERTH, Australia – The independent data safety monitoring board of the global REMAP-CAP COVID-19 study has uncovered a concerning safety signal in treatment arms that include an angiotensin converting enzyme inhibitor and an angiotensin receptor blocker in patients with severe COVID-19, and it has recommended that recruitment be suspended for those treatment arms.
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Elderly patient in hospital bed

Olumiant reduces risk of COVID-19 death, as Recovery trial continues

March 3, 2022
By Nuala Moran
LONDON – The U.K. Recovery trial has added a fourth drug to the list of therapies it has shown are effective in treating hospitalized COVID-19 patients, demonstrating the JAK inhibitor Olumiant (baricitinib) reduces the risk of death by 13% in seriously ill patients. That effect is in addition to treatment with dexamethasone, which became standard of care after the Recovery trial showed it reduced mortality by one-third in patients on ventilators.
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Other news to note for March 3, 2022

March 3, 2022
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: A2, Aquestive, Athira, Autolus, Avenge, Haisco, Inspirevax, Oragenics, Sorrento, Spexis.
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