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BioWorld - Friday, May 15, 2026
Home » Topics » Infection » Coronavirus

Coronavirus
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‘Third’ party: ACIP backs FDA move to add COVID-19 shot for some

Aug. 13, 2021
By Randy Osborne
The CDC’s Advisory Committee on Immunization Practices (ACIP) deliberated the matter of third COVID-19 shots, with panel members voting whether to recommend “additional doses of mRNA COVID-19 vaccines as part of a primary [two-shot] series” in certain immunocompromised patients. A work group set up by ACIP decided previously that the desirable consequences outweighed undesirable ones in such a population.
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Regulatory actions for Aug. 13, 2021

Aug. 13, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Aprea, Biontech, Cytodyn, Immune-Onc, Ipsen, Jazz, Moderna, Novatek, Pfizer, Rigel.
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Other news to note for Aug. 13, 2021

Aug. 13, 2021
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Advanced Chemotherapy, Ampio, Bexson, Cytocom, Fusion, Moderna, Mustang, Nyrada, RDIF, Sen-Jam, Theratechnologies.
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In the clinic for Aug. 13, 2021

Aug. 13, 2021
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Atea, Azurrx, Cali, Equillium, Gigagen, Innovent, Innovation, Longeveron, Lynk, Medivir, Phasebio, Trigone, Ultimovacs, Valneva.
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Vaccine administration

FDA allows mRNA vaccine booster for some immunocompromised patients

Aug. 13, 2021
By Lee Landenberger
The FDA has made allowances for a third COVID-19 vaccine dose to protect certain adults with compromised immune systems. The amended emergency use authorization amendments allow for booster doses of mRNA vaccines from Pfizer Inc.-Biontech SE and Moderna Inc.
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Regulatory actions for Aug. 12, 2021

Aug. 12, 2021
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Coopercompanies, Cytosorbents, Diacarta, Speedx, Syntr Health Technologies.
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U.S. vaccine illustration

FDA action on boosters for the immunocompromised could come soon

Aug. 12, 2021
By Lee Landenberger
According to the White House, the FDA is poised to allow COVID-19 booster shots from Pfizer Inc. and Moderna Inc., the two mRNA vaccines, but only for those people with compromised immune systems. The FDA announcement was anticipated to be as early as today, Aug. 12, and the boosters could be available as quickly as this coming weekend.
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Celltrion-Regkirona-2-9

Celltrion wins Anvisa approval for COVID-19 antibody in first nod outside Asia

Aug. 12, 2021
By Gina Lee
Celltrion Inc. has bagged its first green light outside Asia for its COVID-19 monoclonal antibody Regkirona (regdanvimab) with an emergency use authorization in Brazil. Brazil’s Anvisa gave the EUA for the drug to treat high-risk adult patients, including those aged 65 or older, with mild and moderate COVID-19 symptoms on Aug. 11. The regulator reached its decision on the drug, also known as CT-P59, via a unanimous vote.
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Other news to note for Aug. 12, 2021

Aug. 12, 2021
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Antheia, Artiva, Atai, GC Labcell, Ginkgo, Introspect, Johnson & Johnson, Nimbus, Nobelpharma, Novartis, Novozymes, Noxopharm, Probiogen, Revixia, Schrödinger, Sunshine, Vyne, WHO.
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Microscope and coronavirus illustration

Marker of neuroaxonal injury is also a marker of worse outcomes in COVID-19 patients

Aug. 12, 2021
A proportion of patients with COVID-19 develop neurological symptoms, including headaches, encephalopathy and seizures, but it is unknown to which extent.
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