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BioWorld - Thursday, June 1, 2023
Home » Topics » Infection » Coronavirus

Coronavirus
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Remdesivir capsule

Fauci calls remdesivir 'new standard of care' for COVID-19 as FDA works with Gilead to aid drug’s availability

April 29, 2020
By Michael Fitzhugh
No Comments
Following revelations that a randomized, placebo-controlled study of the Gilead Sciences Inc.’s antiviral, remdesivir, reduced time to recovery for hospitalized patients with "advanced" COVID-19, along with additional data from an open-label phase III trial from its maker, the FDA is "working with Gilead to figure out a mechanism to make this easily available to people who need it," Anthony Fauci, director of the NIH’s National Institute for Allergy and Infectious Diseases (NIAID), said April 29.
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Coronavirus and DNA

Capricor’s COVID-19 success gets FDA and market attention

April 29, 2020
By Lee Landenberger
No Comments
Six of six critically ill COVID-19 patients survived after being treated as compassionate care cases with Capricor Therapeutics Inc.’s lead candidate, an off-the-shelf cardiac cell therapy. The success prompted the FDA to review the data and approve the company’s expanded access protocol for treating as many as 20 more COVID-19 patients.
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Wall Street hails Chimerix viral load; COVID-19, smallpox bids forge onward

April 29, 2020
By Randy Osborne
No Comments
A pair of good-news items from Chimerix Inc. pushed the Durham, N.C.-based company’s stock (NASDAQ:CMRX) to $2.15, closing up 64 cents, or 42%, higher as backers reacted to near-term NDA plans for smallpox countermeasure brincidofovir (BCV) and the start of a phase II/III trial with dociparstat sodium (DSTAT) in COVID-19 patients with acute lung injury (ALI).
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Aussie biotechs scramble to raise funds to save cash as capital tightens, trials stall

April 29, 2020
By Tamra Sami
No Comments
PERTH, Australia – Roughly 40% of Australia’s biotech companies are seeking capital as they feel the pinch from international travel bans that seriously hamper capital raising, according to a recent Ausbiotech survey.
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Redhill looks to extend opaganib access following positive COVID-19 study results

April 29, 2020
By Gina Lee
No Comments
HONG KONG – Israeli biopharma Redhill Biopharma Ltd. is looking to extend access to its new investigational drug, opaganib (Yeliva, ABC-294640), following the drug’s initial success from a compassionate-use study treating six patients in Israel hospitalized with moderate to severe COVID-19 symptoms.
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British flag

Bergenbio’s bemcentinib joins fast-tracked Accord program targeting COVID-19

April 29, 2020
By Nuala Moran
No Comments
LONDON – The U.K. has started a fast track national trial of experimental drugs in COVID-19 patients, with Bergenbio ASA’s phase II cancer immunotherapy, bemcentinib, the first of six products that are due to join the study.
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Regulatory front for April 29, 2020

April 29, 2020
No Comments
The latest global regulatory news, changes and updates affecting biopharma.
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Other news to note for April 29, 2020

April 29, 2020
No Comments
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Adicet, Allogene, Almac, Batavia, Beam, Catalent, Edigene, Editas, Fate, Haima, Johnson & Johnson, Heat, Innovative Cellular, Magenta, Merck, Preveceutical Medical, Proteogenix, Restorbio, Revolution Medicines, Rubius, Sanofi, Supernus, Worldmeds, Venatorx, Verndari.
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In the clinic for April 29, 2020

April 29, 2020
No Comments
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Biontech, Cadent, Chimerix, Corbus, Destiny, Dynavax, Erytech, Geneone, Gilead, Gracell, Inovio, Pfizer, United Therapeutics, Windtree.
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U.S. flag and White House podium

White House proposes two antibody tests per patient in updated COVID-19 plan

April 28, 2020
By Mark McCarty
No Comments
The Trump administration has posted an update to its plan to reopen the U.S. economy, this time with a slightly different twist on testing. This plan not only calls on local governments to administer tests for the SARS-CoV-2 virus, but also calls for two antibody tests per person under some circumstances, an approach that should beef up both the positive and negative predictive values compared to a single antibody test.
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