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Home / COVID-19 - Page 12

COVID-19

Novavax filed in the EU for expanded conditional Marketing Authorization of COVID-19 vaccine as booster in individuals aged 18 and over
Biotechnology | COVID-19 | Infectious Disease | Vaccine

Novavax filed in the EU for expanded conditional Marketing Authorization of COVID-19 vaccine as booster in individuals aged 18 and over

On May 20, 2022, Novavax announced the submission of a request to the European Medicines Agency (EMA) to…

Read More Novavax filed in the EU for expanded conditional Marketing Authorization of COVID-19 vaccine as booster in individuals aged 18 and overContinue

Depression, loneliness associated with increased hospitalization risk after COVID-19
COVID-19 | Diagnostics | NIH | Therapeutics

Depression, loneliness associated with increased hospitalization risk after COVID-19

On May 19, 2022, the U.S. National Institutes of Health (NIH) announced that people who reported in a…

Read More Depression, loneliness associated with increased hospitalization risk after COVID-19Continue

WHO validated 11th vaccine for COVID-19
COVID-19 | Life Science History | Vaccine | WHO

WHO validated 11th vaccine for COVID-19

On May 19, 2022, WHO issued an emergency use listing (EUL) for CONVIDECIA, a vaccine manufactured by CanSino…

Read More WHO validated 11th vaccine for COVID-19Continue

NIH announced antiviral drug development awards
COVID-19 | Life Science History

NIH announced antiviral drug development awards

On May 18, 2022, the U.S. National Institutes of Health announced it had awarded approximately $577 million to…

Read More NIH announced antiviral drug development awardsContinue

Labcorp received EUA for first non-prescription at-home collection kit for combined COVID-19, Fflu and RSV detection
Biotechnology | COVID-19 | Diagnostics | Infectious Disease | Influenza

Labcorp received EUA for first non-prescription at-home collection kit for combined COVID-19, Fflu and RSV detection

On May 18, 2022, LabCorp announced the receipt of Emergency Use Authorization (EUA) from the U.S. Food and…

Read More Labcorp received EUA for first non-prescription at-home collection kit for combined COVID-19, Fflu and RSV detectionContinue

InteliSwabᆴ COVID-19 rapid test validated to detect Omicron BA.2, BA.2.12.1, BA.3 and BA.5 subvariants
COVID-19 | Life Science History

InteliSwabᆴ COVID-19 rapid test validated to detect Omicron BA.2, BA.2.12.1, BA.3 and BA.5 subvariants

On May 17, 2022, OraSure Technologies announced that its InteliSwabᆴ COVID-19 rapid tests detect the Omicron BA.2, BA.2.12.1,…

Read More InteliSwabᆴ COVID-19 rapid test validated to detect Omicron BA.2, BA.2.12.1, BA.3 and BA.5 subvariantsContinue

Pfizer and BioNTech granted U.S. EUA for booster dose of COVID-19 vaccine in children 5 through 11 years of age
COVID-19 | Life Science History

Pfizer and BioNTech granted U.S. EUA for booster dose of COVID-19 vaccine in children 5 through 11 years of age

On May 17, 2022, Pfizer and BioNTech announced the U.S. Food and Drug Administration expanded emergency use authorization…

Read More Pfizer and BioNTech granted U.S. EUA for booster dose of COVID-19 vaccine in children 5 through 11 years of ageContinue

TGen worked with Arizona zoos and state and federal wildlife agencies to test wild animals for SARS-CoV-2
COVID-19 | Life Science History

TGen worked with Arizona zoos and state and federal wildlife agencies to test wild animals for SARS-CoV-2

On May 16, 2022, working with state and federal wildlife agencies and private and public zoos across Arizona,…

Read More TGen worked with Arizona zoos and state and federal wildlife agencies to test wild animals for SARS-CoV-2Continue

Novavax filed for Emergency Use Authorization of COVID-19 vaccine in Taiwan
Biotechnology | COVID-19 | Infectious Disease | Vaccine

Novavax filed for Emergency Use Authorization of COVID-19 vaccine in Taiwan

On May 13, 2022, Novavax announced the submission of a request for emergency use authorization to Taiwan’s Food…

Read More Novavax filed for Emergency Use Authorization of COVID-19 vaccine in TaiwanContinue

WHO and Medicines Patent Pool announced agreement with NIH for COVID-19 health technologies
COVID-19 | Life Science History | Vaccine | WHO

WHO and Medicines Patent Pool announced agreement with NIH for COVID-19 health technologies

On May 12, 2022, WHOメs COVID-19 Technology Access Pool and the Medicines Patent Pool finalized a licensing agreement…

Read More WHO and Medicines Patent Pool announced agreement with NIH for COVID-19 health technologiesContinue

Cepheid received Emergency Use Authorization for Xpertᆴ Xpress CoV-2 plus
COVID-19 | Life Science History

Cepheid received Emergency Use Authorization for Xpertᆴ Xpress CoV-2 plus

On May 12, 2022, Cepheid announced it had received Emergency Use Authorization from the U.S. Food & Drug…

Read More Cepheid received Emergency Use Authorization for Xpertᆴ Xpress CoV-2 plusContinue

NIH licensed COVID-19 research tools and early-stage technologies to WHO program
COVID-19 | Life Science History | Vaccine

NIH licensed COVID-19 research tools and early-stage technologies to WHO program

On May 12, 2022, the U.S. National Institutes of Health announced that it had licensed 11 COVID-19 research…

Read More NIH licensed COVID-19 research tools and early-stage technologies to WHO programContinue

Lucira filed for authorization of first-of-its-Kind COVID-19 & flu at-home molecular test
COVID-19 | Life Science History

Lucira filed for authorization of first-of-its-Kind COVID-19 & flu at-home molecular test

On May 11, 2022, Lucira Health announced that it had submitted a request to the U.S. Food and…

Read More Lucira filed for authorization of first-of-its-Kind COVID-19 & flu at-home molecular testContinue

KPWHRI report supported value of COVID-19 drugs
Biotechnology | COVID-19 | Infectious Disease | Non-Profit Research | Therapeutics

KPWHRI report supported value of COVID-19 drugs

On May 11, 2022, Kaiser Permanente Washington Health Research Institute reported that new treatments for people at high…

Read More KPWHRI report supported value of COVID-19 drugsContinue

Lucira received CE Mark for both COVID-19 & flu and COVID-19 molecular tests
COVID-19 | Life Science History

Lucira received CE Mark for both COVID-19 & flu and COVID-19 molecular tests

On May 9, 2022, Lucira Health announced that both its COVID-19 & Flu and COVID-19 molecular tests have…

Read More Lucira received CE Mark for both COVID-19 & flu and COVID-19 molecular testsContinue

Novavax submitted variations to expand Australian and New Zealand provisional approval of Nuvaxovid COVID-19 vaccine in Great Britain
Biotechnology | COVID-19 | Infectious Disease | Vaccine

Novavax submitted variations to expand Australian and New Zealand provisional approval of Nuvaxovid COVID-19 vaccine in Great Britain

On May 6, 2022, Novavax announced the submission of variations to the Australian Therapeutic Goods Agency (TGA) and…

Read More Novavax submitted variations to expand Australian and New Zealand provisional approval of Nuvaxovid COVID-19 vaccine in Great BritainContinue

Novavax’s COVID-19 vaccine Nuvaxovid arrived in Singapore
Biotechnology | COVID-19 | Infectious Disease | Vaccine

Novavax’s COVID-19 vaccine Nuvaxovid arrived in Singapore

On May 6, 2022, Novavax announced that deliveries of it’s COVID-19 vaccine continued around the world and the…

Read More Novavax’s COVID-19 vaccine Nuvaxovid arrived in SingaporeContinue

WHO reported 14.9 million excess deaths associated with the COVID-19 pandemic in 2020 and 2021
COVID-19 | Life Science History | WHO

WHO reported 14.9 million excess deaths associated with the COVID-19 pandemic in 2020 and 2021

On May 5, 2022, the World Health Organization (WHO) reported estimates that show the full death toll associated…

Read More WHO reported 14.9 million excess deaths associated with the COVID-19 pandemic in 2020 and 2021Continue

Sorrento announced full enrollment of phase I study of intranasal STI-9199 (COVISHIELD) against Omicron BA.2 and all variants of concern
Biotechnology | COVID-19

Sorrento announced full enrollment of phase I study of intranasal STI-9199 (COVISHIELD) against Omicron BA.2 and all variants of concern

On May 2, 2022, Sorrento announced its Phase I study of intranasal STI-9199 (COVISHIELDTM) had been fully enrolled…

Read More Sorrento announced full enrollment of phase I study of intranasal STI-9199 (COVISHIELD) against Omicron BA.2 and all variants of concernContinue

Moderna finalized plan for long-term strategic partnership with the Government of Canada
Biotechnology | COVID-19 | Infectious Disease | Vaccine

Moderna finalized plan for long-term strategic partnership with the Government of Canada

On Apr. 29, 2022, Moderna announced its plan to build a state-of-the-art mRNA vaccine manufacturing facility in Quebec…

Read More Moderna finalized plan for long-term strategic partnership with the Government of CanadaContinue

Moderna filed to expand conditional Marketing Authorization for COVID-19 vaccine to include children six months to under six years in the EU
Biotechnology | COVID-19 | Infectious Disease | Vaccine

Moderna filed to expand conditional Marketing Authorization for COVID-19 vaccine to include children six months to under six years in the EU

On Apr. 29, 2022, Moderna announced that it had submitted for a variation to the conditional marketing authorization…

Read More Moderna filed to expand conditional Marketing Authorization for COVID-19 vaccine to include children six months to under six years in the EUContinue

Moderna filed for authorization of Its COVID-19 vaccine in young children six months to under six years of age
Biotechnology | COVID-19 | FDA | Infectious Disease | Vaccine

Moderna filed for authorization of Its COVID-19 vaccine in young children six months to under six years of age

On Apr. 28, 2022, Moderna announced that it had submitted a request for emergency use authorization (EUA) for…

Read More Moderna filed for authorization of Its COVID-19 vaccine in young children six months to under six years of ageContinue

Pfizer and BioNTech submitted application for U.S. EUA for COVID-19 vaccine booster dose in children 5 through 11 years of age
Biotechnology | COVID-19 | FDA | Vaccine

Pfizer and BioNTech submitted application for U.S. EUA for COVID-19 vaccine booster dose in children 5 through 11 years of age

On Apr. 26, 2022, Pfizer and BioNTech submitted an application to the U.S. Food and Drug Administration (FDA)…

Read More Pfizer and BioNTech submitted application for U.S. EUA for COVID-19 vaccine booster dose in children 5 through 11 years of ageContinue

Veklury (Remdesivir) was first and only approved treatment for pediatric patients under 12 years of age with COVID-19
Biotechnology | COVID-19 | FDA | Infectious Disease

Veklury (Remdesivir) was first and only approved treatment for pediatric patients under 12 years of age with COVID-19

On Apr. 25, 2022, Gilead Sciences announced that the U.S. Food and Drug Administration (FDA) has approved a supplemental…

Read More Veklury (Remdesivir) was first and only approved treatment for pediatric patients under 12 years of age with COVID-19Continue

Novavax announced initiation of COVID-19 vaccine booster study in adolescents in phase 3 PREVENT-19 trial
Biotechnology | COVID-19 | Infectious Disease | Vaccine

Novavax announced initiation of COVID-19 vaccine booster study in adolescents in phase 3 PREVENT-19 trial

On Apr. 22, 2022, Novavax announced initial results from the Phase 1/2 clinical trial of its COVID-Influenza Combination…

Read More Novavax announced initiation of COVID-19 vaccine booster study in adolescents in phase 3 PREVENT-19 trialContinue

WHO recommended Paxlovid for high-risk COVID patients
Biotechnology | COVID-19 | Infectious Disease | Therapeutics | WHO

WHO recommended Paxlovid for high-risk COVID patients

On Apr. 22, 2022, the World Health Organization (WHO) made a strong recommendation for nirmatrelvir and ritonavir, sold…

Read More WHO recommended Paxlovid for high-risk COVID patientsContinue

Cocrystal Pharma collaborated with the NIAID to evaluate COVID-19 protease inhibitors
Biotechnology | COVID-19 | Therapeutics

Cocrystal Pharma collaborated with the NIAID to evaluate COVID-19 protease inhibitors

On Apr. 21, 2022, Cocrystal Pharma announced a Non-Clinical Evaluation Agreement with the National Institute of Allergy and…

Read More Cocrystal Pharma collaborated with the NIAID to evaluate COVID-19 protease inhibitorsContinue

CureVac and GSKメs bivalent second-generation mRNA accine candidate shown to be highly effective against SARS-CoV-2 variants
COVID-19 | Life Science History | Vaccine

CureVac and GSKメs bivalent second-generation mRNA accine candidate shown to be highly effective against SARS-CoV-2 variants

On Apr. 21, 2022, CureVac announced preclinical data demonstrating immune responses and protective efficacy of a bivalent second-generation…

Read More CureVac and GSKメs bivalent second-generation mRNA accine candidate shown to be highly effective against SARS-CoV-2 variantsContinue

Initial results from Novavax’ COVID-19-Influenza vaccine trial were first to show feasibility of combination vaccine
Biotechnology | COVID-19 | Infectious Disease | Influenza | Vaccine

Initial results from Novavax’ COVID-19-Influenza vaccine trial were first to show feasibility of combination vaccine

On Apr. 20, 2022, Novavax announced initial results from the Phase 1/2 clinical trial of its COVID-Influenza Combination…

Read More Initial results from Novavax’ COVID-19-Influenza vaccine trial were first to show feasibility of combination vaccineContinue

Tonix Pharm announced results of retrospective observational database study in over 50,000 long COVID patients
Biotechnology | COVID-19 | Diagnostics | Infectious Disease | Therapeutics

Tonix Pharm announced results of retrospective observational database study in over 50,000 long COVID patients

On Apr. 20, 2022, Tonix Pharmaceuticals announced the results of a retrospective observational database study in over 50,000…

Read More Tonix Pharm announced results of retrospective observational database study in over 50,000 long COVID patientsContinue

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