Dec 23, 2020 · SAN DIEGO, Dec. 22, 2020 (GLOBE NEWSWIRE) — Sorrento Therapeutics, Inc. (Nasdaq: SRNE, “Sorrento”) today announced that an Emergency Use Authorization (EUA) Application has been submitted to the US Food and Drug Administration for its COVI-STIX rapid diagnostic test for the detection of the SARS-CoV-2 virus nucleocapsid antigen in nasal samples of patients.
Aug 27, 2020 · FDA approves $5 rapid coronavirus test that doesn't require special computer. August 27, 2020 / 1:27 PM / AP CDC loosens coronavirus testing procedure guidelines .
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Sorrento Therapeutics has seen progress in the development of the antibody STI-1499, which could serve as an effective treatment in blocking the virus.

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  • Shares of Sorrento Therapeutics spiked 8% in Wednesday's pre-market trading after the drugmaker filed for emergency use of its COVID-19 test with the US Food and Drug Administration (FDA ...
  • Cardiol Therapeutics Receives FDA Approval for Investigational New Drug (IND) Application . for Phase II/III COVID-19 Trial . Trial will take place at major U.S. centers and examine the cardioprotective properties of CardiolRx™ in patients hospitalized with COVID-19 who have a . prior history of, or risk factors for, cardiovascular disease (CVD)

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Oct 14, 2020 · October 14, 2020. COVID-19, Rare Disease. Waking up to the news has one encouraging note, another new day and another new drug is being tested. According to an article in Biospace, the news from Sorrento Therapeutics has double the significance with STI-2020 and STI-1499 neutralizing antibodies exhibiting protection against the SARS-CoV-2 infection in a Syrian golden hamster model.

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  • Sorrento Therapeutics Inc (NASDAQ: SRNE ) shares, which have been given to much volatility , are rallying sharply Friday. ... The company hopes to win FDA approval to ...
  • Sorrento Therapeutics (SRNE) - Get Report shares skyrocketed Thursday after the biopharmaceutical company received Food and Drug Administration approval for a Phase 1 trial of its neutralizing...

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On Monday, Sorrento Therapeutics received clearance from the FDA to initiate a Phase 2 trial of Abivertinib in patients with COVID-19 who have moderate to severe pulmonary symptoms. That trial could begin as soon as August. Sorrento's stock spiked at the start of this week as a result of the encouraging news. Abivertinib has already completed a registration trial for lung cancer and been ...

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Jul 01, 2020 · Dr. Henry Ji, Chairman and CEO of Sorrento Therapeutics, said, “If successful and approved, we plan to produce the T-VIVA-19 vaccine in our therapeutic antibody cGMP production facility in San ...

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Sorrento Therapeutics Inc (NASDAQ: SRNE ) shares, which have been given to much volatility , are rallying sharply Friday. ... The company hopes to win FDA approval to ...

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ZURICH (Reuters) – Relief Therapeutics said on Wednesday it and U.S. partner NeuroRx asked the U.S. Food and Drug Administration for emergency approval for a drug it aims to repurpose against COVID-19, citing a 51-person study the Swiss drugmaker said showed the medicine helped sick patients.

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Jul 29, 2020 · Sorrento Therapeutics has developed a portfolio of COVID-19 solutions and operates a state of the art cGMP facility here in San Diego. The exclusive license with Sorrento Therapeutics will offer...

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Oct 01, 2020 · Henry Ji, Sorrento’s CEO, told Gomez that unlike vaccines, these antibody trials can speed from Phase 1 to Phase 3 in just weeks, raising hopes for a safe and effective COVID-19 treatment in the ...

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