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BioWorld - Monday, April 13, 2026
Home » Topics » Infection » Coronavirus

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Regulatory front

FDA: COVID-19 shows why diversity needed in trials

Nov. 9, 2020
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma, including: Final analysis: hydroxychloroquine offers no benefit; FDA finalizes PDUFA VI fee guidance.
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Antibodies attacking SARS-CoV-2 virus

Memo trains convalescent antibody on COVID-19

Nov. 6, 2020
By Cormac Sheridan
DUBLIN – Memo Therapeutics AG raised CHF13.8 million (US$15.3 million) in a first close of a series B round to take forward a patient-derived monoclonal antibody therapy for COVID-19, MTX-Covab, which will move into a phase I/II trial in Germany in the new year.
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Regulatory actions for Nov. 6, 2020

Nov. 6, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Elekta, Genscript.
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Other news to note for Nov. 6, 2020

Nov. 6, 2020
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Bioelectronics, Careprotocol, Decision Diagnostics, Djo, Genassist, Hancock Jaffe, Mesa Biotech, Orthoalign, Progenity, Scott Specialties, Verida.
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Regulatory front

FDA authorizes serology test for neutralizing antibodies

Nov. 6, 2020
By Mark McCarty
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: FDA tweaks export final guidance per CARES Act; OIG: CMS should act to recover payments for device credits.
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Humanigen’s twice as nice COVID-19 bump for lenzilumab

Nov. 6, 2020
By Lee Landenberger
Lenzilumab, the lead candidate from Humanigen Inc., has taken two large steps forward with positive interim phase III data and some support from the federal government. That, along with an Asia-Pacific region licensing from earlier in the week, has the relatively small company successfully “punching above our weight,” the CEO told BioWorld.
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Patient in hospital bed

Canakinumab flunks phase III trial in COVID-19

Nov. 6, 2020
By Cormac Sheridan
DUBLIN – Canakinumab, an interleukin-1 beta (IL-1beta) inhibitor, has joined a growing list of immunomodulatory therapies that have failed to demonstrate efficacy in COVID-19. Novartis AG said that an interim analysis showed the drug did not meet the primary endpoint of clinical response.
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Sichuan Clover Biopharmaceuticals' COVID-19 vaccine boosted by CEPI

Nov. 6, 2020
By Sergio Held
The Coalition for Epidemic Preparedness Innovations (CEPI) said that it would fund a SARS-CoV-2 vaccine under development by Sichuan Clover Biopharmaceuticals Inc., of Chengdu, China.
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Regulatory front

PTO sees spike in patent applications reciting AI

Nov. 6, 2020
By Mark McCarty
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: NICE reviews Dexcom’s G6; Ortho claims EUA for antigen test with 100% sensitivity.
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Regulatory actions for Nov. 6, 2020

Nov. 6, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Astrazeneca, Astellas, Basilea, Gosun, Bristol Myers Squibb, Lipocine, Sarepta, Sedor, Senhwa.
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