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BioWorld - Wednesday, January 21, 2026
Home » Topics » Infection » Coronavirus

Coronavirus
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Glenmark’s phase III favipiravir study finds drug speeds clinical improvement for some patients

July 28, 2020
By David Ho
HONG KONG – Mumbai, India-headquartered Glenmark Pharmaceuticals Ltd. have released statistically significant top-line results from a phase III trial showing that Fabiflu (favipiravir), an antiviral pyrazine RNA polymerase inhibitor, can treat cases of mild to moderate COVID-19 in four days.
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Antibodies attacking SARS-CoV-2 virus

Exevir launches with COVID-19 candidate, plans for antiviral platform

July 28, 2020
By Nuala Moran
LONDON - The combined force of Belgian life sciences has been brought together in the launch of Exevir Bio BV, which arrives on the scene with a €23 million (US$27 million) series A and ready for a phase I study of its novel antiviral therapy in hospitalized COVID-19 patients.
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Regulatory actions for July 28, 2020

July 28, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Apogenix, Black Diamond, Chi-Med, Foresee, Hemoshear, Larimar, Momenta, Nabriva, Protara, Realta.
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Other news to note for July 28, 2020

July 28, 2020
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: AC Immune, Acerus, Agenus, Anixa, Axial, Bayer, Bergenbio, Betta, Chi-Med, Crescita, Cure, Futurx, Gilead, Grifols, Hansoh, Humanigen, Iacta, Imcyse, Immunome Karuna, Lumos, Merck, Nascent, Osmotica, PGI, Promedica, Recursion, Restorbio, Santen, Schrodinger, Selecta, Sobi, Sol-Gel, Soligenix, Stemedica, Taro, Terns, Theragen, Tscan, Viva, Zhaoke.
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Regulatory front for July 28, 2020

July 28, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Abbvie, Amgen, Indivior, Mylan, Pfizer, Sandoz, Taro.
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COVID-19, coronavirus paper dolls

FDA revises Labcorp EUA for screening of those without known or suspected COVID-19

July 27, 2020
By Mark McCarty
The U.S. FDA has rewritten the emergency use authorization (EUA) for the Laboratory Corp. of America Holdings Inc. (Labcorp) COVID-19 polymerase chain reaction (PCR) test to allow for diagnostic testing of those who are asymptomatic and those who have no reason to suspect they are infected with the SARS-CoV-2 virus.
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Regulatory front for July 27, 2020

July 27, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Fortress Diagnostics, Lemaitre Vascular, MedPAC.
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Regulatory actions for July 27, 2020

July 27, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Color, Labcorp, Rapid Medical, Stratus Medical, Zebra Medical.
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Other news to note for July 27, 2020

July 27, 2020
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Atox, Bruker, Cell and Gene Therapy Catapult, Cpi, Healthimation, Masimo, Microfluidx, Nanthealth, Nemaura, OpenNMS, Orcam, Perimeter Medical Imaging, Telix Japan, Transenterix, Wishbone Medical.
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Moderna searches for the right participants in its phase III COVID-19 trial

July 27, 2020
By Lee Landenberger
Moderna Inc. dosed the first of what could be as many as 30,000 healthy volunteers Monday morning as it began its phase III COVID-19 vaccine trial.
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