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Home / COVID-19 - Page 80

COVID-19

Sinovac announced first animal study results of vaccine against COVID-19 published in SCIENCE
COVID-19 | Life Science History | Vaccine

Sinovac announced first animal study results of vaccine against COVID-19 published in SCIENCE

On May 6, 2020, Sinovac Biotech announced publication of the preclinical study on animals for its vaccine candidate…

Read More Sinovac announced first animal study results of vaccine against COVID-19 published in SCIENCEContinue

Miami University confirmed high quality of IGEA’s COVID-19 rapid test
Biotechnology | COVID-19 | Life Science History

Miami University confirmed high quality of IGEA’s COVID-19 rapid test

On May 6, 2020, IGEA Pharma announced that an evaluation by the University of Miami Miller School of…

Read More Miami University confirmed high quality of IGEA’s COVID-19 rapid testContinue

bioMerieux serology tests for SARS-CoV-2 on VIDAS underwent validation preceding launch
Biotechnology | COVID-19

bioMerieux serology tests for SARS-CoV-2 on VIDAS underwent validation preceding launch

On May 6, 2020, bioMerieux announced performance validation and the launch of VIDAS anti-SARS-CoV-2 serology tests to detect…

Read More bioMerieux serology tests for SARS-CoV-2 on VIDAS underwent validation preceding launchContinue

Laurent Pharmaceuticals received Health Canada’s approval to initiate COVID-19 clinical trial
Biotechnology | COVID-19 | Infectious Disease | Pharmaceutical | Therapeutics

Laurent Pharmaceuticals received Health Canada’s approval to initiate COVID-19 clinical trial

On May 6, 2020, Laurent Pharmaceuticals announced that it has obtained the approval from Health Canada to initiate…

Read More Laurent Pharmaceuticals received Health Canada’s approval to initiate COVID-19 clinical trialContinue

First patient dosed in FDA-approved phase III lenzilumab study for COVID-19
COVID-19 | Life Science History

First patient dosed in FDA-approved phase III lenzilumab study for COVID-19

On May 6, 2020, Humanigen announced that the first COVID-19 patient had been dosed in its previously announced…

Read More First patient dosed in FDA-approved phase III lenzilumab study for COVID-19Continue

3M and Ford begin shipping newly designed powered air-purifying respirators for health care workers fighting COVID-19
COVID-19 | Life Science History

3M and Ford begin shipping newly designed powered air-purifying respirators for health care workers fighting COVID-19

On May 6, 2020, 3M and Ford announced that newly designed powered air-purifying respirators (PAPRs), developed are on…

Read More 3M and Ford begin shipping newly designed powered air-purifying respirators for health care workers fighting COVID-19Continue

Predictive Oncology launched new AI platform for vaccine and drug development targeting coronaviruses and Acute Respiratory Syndromes
COVID-19 | Influenza | Life Science History | Nanotechnology | NIH | Vaccine

Predictive Oncology launched new AI platform for vaccine and drug development targeting coronaviruses and Acute Respiratory Syndromes

On May 6, 2020, Predictive Oncology announced the acquisition of Soluble Therapeutics and partnership and licensing of a…

Read More Predictive Oncology launched new AI platform for vaccine and drug development targeting coronaviruses and Acute Respiratory SyndromesContinue

Meridian Bioscience partnered with QuantuMDx on COVID-19 assay
COVID-19 | Life Science History

Meridian Bioscience partnered with QuantuMDx on COVID-19 assay

On May 6, 2020, Meridian Bioscience announced a collaboration with QuantuMDx on its newly launched SARS-CoV-2 assay for…

Read More Meridian Bioscience partnered with QuantuMDx on COVID-19 assayContinue

FDA provided Emergency Use Authorization to PerkinElmer for serological test to identify COVID-19 antibodies
Biotechnology | COVID-19 | Diagnostics | FDA

FDA provided Emergency Use Authorization to PerkinElmer for serological test to identify COVID-19 antibodies

On May 5, 2020, PerkinElmer announced the FDA provided Emergency Use Authorization (EUA) for EUROIMMUN’s (a PerkinElmer company)…

Read More FDA provided Emergency Use Authorization to PerkinElmer for serological test to identify COVID-19 antibodiesContinue

Medigen Vaccine Biologics signed a license agreement with NIH on COVID-19 vaccine
COVID-19 | Life Science History | NIH | Vaccine

Medigen Vaccine Biologics signed a license agreement with NIH on COVID-19 vaccine

On May 5, 2020, Medigen Vaccine Biologics (MVB) announced a global commercial license agreement with National Institutes of…

Read More Medigen Vaccine Biologics signed a license agreement with NIH on COVID-19 vaccineContinue

TGen and HonorHealth initiated COVID-19 combination therapy of atovaquone and azithromycin  in patients with moderate-to-severe COVID-19 infection
COVID-19 | Life Science History

TGen and HonorHealth initiated COVID-19 combination therapy of atovaquone and azithromycin in patients with moderate-to-severe COVID-19 infection

On May 5, 2020, the HonorHealth Research Institute and HonorHealth announced the successful enrollment on a novel combination…

Read More TGen and HonorHealth initiated COVID-19 combination therapy of atovaquone and azithromycin in patients with moderate-to-severe COVID-19 infectionContinue

Organicell announces FDA approval of IND application for treatment of SARS due to COVID-19
COVID-19 | FDA | Life Science History

Organicell announces FDA approval of IND application for treatment of SARS due to COVID-19

On May 5, 2020, Organicell Regenerative Medicine announced the FDA has approved the Investigational New Drug application for…

Read More Organicell announces FDA approval of IND application for treatment of SARS due to COVID-19Continue

Tyson Foods Fresh Meats resumed Waterloo, Iowa operations
Agriculture | Biotechnology | COVID-19 | Diagnostics | Infectious Disease | Vaccine

Tyson Foods Fresh Meats resumed Waterloo, Iowa operations

On May 5, 2020, Tyson Foods announced resumption of limited production at its Waterloo, Iowa facility May 7….

Read More Tyson Foods Fresh Meats resumed Waterloo, Iowa operationsContinue

Innovation Pharma announced the next phase of Brilacidin Coronavirus testing begun
COVID-19 | Life Science History

Innovation Pharma announced the next phase of Brilacidin Coronavirus testing begun

On May 5, 2020, Innovation Pharma reported it had executed a Material Transfer Agreement (MTA) with a leading…

Read More Innovation Pharma announced the next phase of Brilacidin Coronavirus testing begunContinue

Massachusetts Eye and Ear and Massachusetts General Hospital advancied gene-based COVID-19 vaccine
COVID-19 | Life Science History | Vaccine

Massachusetts Eye and Ear and Massachusetts General Hospital advancied gene-based COVID-19 vaccine

On May 5, 2020, Massachusetts Eye and Ear and Massachusetts General Hospital (MGH), members of Mass General Brigham,…

Read More Massachusetts Eye and Ear and Massachusetts General Hospital advancied gene-based COVID-19 vaccineContinue

LabCorp announced availability of COVID-19 antibody test
Biotechnology | COVID-19 | Medical Device

LabCorp announced availability of COVID-19 antibody test

On May 5, 2020, LabCorp announced that its COVID-19 Immunoglobulin G (IgG) antibody test is now available for…

Read More LabCorp announced availability of COVID-19 antibody testContinue

Pfizer and BioNTech dosed first participants in US as part of global COVID-19 mRNA vaccine development program
COVID-19 | Life Science History | Vaccine

Pfizer and BioNTech dosed first participants in US as part of global COVID-19 mRNA vaccine development program

On May 5, 2020, Pfizer and BioNTech announced the first participants have been dosed in the U.S. in…

Read More Pfizer and BioNTech dosed first participants in US as part of global COVID-19 mRNA vaccine development programContinue

Athersys announced commencement of patient enrollment in MACOVIA Study, a pivotal phase 2/3 trial evaluating MultiStemᆴ cell therapy for COVID-19 induced ARDS
COVID-19 | Life Science History

Athersys announced commencement of patient enrollment in MACOVIA Study, a pivotal phase 2/3 trial evaluating MultiStemᆴ cell therapy for COVID-19 induced ARDS

On May 5, 2020, Athersys announced the first patients have been enrolled in Athersysメ pivotal Phase 2/3 study…

Read More Athersys announced commencement of patient enrollment in MACOVIA Study, a pivotal phase 2/3 trial evaluating MultiStemᆴ cell therapy for COVID-19 induced ARDSContinue

Diffusion Pharma announced FDA Accelerated Review of TSC clinical development plan to treat COVID-19 patients with ARDS
COVID-19 | FDA | Life Science History

Diffusion Pharma announced FDA Accelerated Review of TSC clinical development plan to treat COVID-19 patients with ARDS

On May 5, 2020, Diffusion Pharmaceuticals announced the FDA accelerated its review of the Companyメs clinical development plan…

Read More Diffusion Pharma announced FDA Accelerated Review of TSC clinical development plan to treat COVID-19 patients with ARDSContinue

ACON Laboratories announced international availability of SARS-CoV-2 rapid test
COVID-19 | Life Science History

ACON Laboratories announced international availability of SARS-CoV-2 rapid test

On May 5, 2020, ACON Laboratories announced the availability of its SARS-COV-2 IgG/IgM Rapid Test. ACONメs test is…

Read More ACON Laboratories announced international availability of SARS-CoV-2 rapid testContinue

USPTO launched platform to facilitate connections between patent holders and potential licensees in key technologies
Biotechnology | COVID-19 | Diagnostics | Medical Device | Non-Profit Research | Pharmaceutical | Therapeutics

USPTO launched platform to facilitate connections between patent holders and potential licensees in key technologies

On May 4, 2020, the U.S. Patent and Trademark Office (USPTO) unveiled a new web-based intellectual property marketplace…

Read More USPTO launched platform to facilitate connections between patent holders and potential licensees in key technologiesContinue

BIOFIRE respiratory panel 21 (RP21) with SARS-CoV-2 obtained FDA Emergency Use Authorization
Biotechnology | COVID-19 | FDA

BIOFIRE respiratory panel 21 (RP21) with SARS-CoV-2 obtained FDA Emergency Use Authorization

On May 4, 2020, bioMerieux announced that BioFire Diagnostics, its subsidiary specialized in syndromic infectious disease testing, has…

Read More BIOFIRE respiratory panel 21 (RP21) with SARS-CoV-2 obtained FDA Emergency Use AuthorizationContinue

Vir and Alnylam identified RNAi therapeutic development candidate, VIR-2703 (ALN-COV), targeting SARS-CoV-2 for treatment of COVID-19
Biotechnology | COVID-19 | FDA | Genomics | Infectious Disease | Therapeutics

Vir and Alnylam identified RNAi therapeutic development candidate, VIR-2703 (ALN-COV), targeting SARS-CoV-2 for treatment of COVID-19

On May 4, 2020, Vir Biotech and Alnylam Pharma announced the selection of a development candidate for VIR-2703,…

Read More Vir and Alnylam identified RNAi therapeutic development candidate, VIR-2703 (ALN-COV), targeting SARS-CoV-2 for treatment of COVID-19Continue

Anixa Biosciences and OntoChem announced discovery of first Covid-19 therapeutic candidate
Biotechnology | COVID-19 | Infectious Disease | Therapeutics

Anixa Biosciences and OntoChem announced discovery of first Covid-19 therapeutic candidate

On May 4, 2020, Anixa Biosciences and partner OntoChem, announced they had identified its first therapeutic candidate against…

Read More Anixa Biosciences and OntoChem announced discovery of first Covid-19 therapeutic candidateContinue

NanoViricides signed confidential disclosure agreement with international pharma company to explore collaboration on COVID-19 program
COVID-19 | Life Science History

NanoViricides signed confidential disclosure agreement with international pharma company to explore collaboration on COVID-19 program

On May 4, 2020, NanoViricides announced that it has signed a Confidential Disclosure Agreement with a leading pharmaceutical…

Read More NanoViricides signed confidential disclosure agreement with international pharma company to explore collaboration on COVID-19 programContinue

Eli Lilly and Junshi Biosciences to co-develop antibody therapies for pevention and treatment of COVID-19
COVID-19 | Life Science History

Eli Lilly and Junshi Biosciences to co-develop antibody therapies for pevention and treatment of COVID-19

On May 4, 2020, Junshi Biosciences and Eli Lilly announced an agreement to co-develop therapeutic antibodies for the…

Read More Eli Lilly and Junshi Biosciences to co-develop antibody therapies for pevention and treatment of COVID-19Continue

Mayo Clinic received $26 million from BARDA for COVID-19 convalescent plasma expanded access program
Biotechnology | COVID-19 | Infectious Disease | Non-Profit Research | Therapeutics

Mayo Clinic received $26 million from BARDA for COVID-19 convalescent plasma expanded access program

On May 4, 2020, Mayo Clinic was awarded a $26 million contract from the Biomedical Advanced Research and…

Read More Mayo Clinic received $26 million from BARDA for COVID-19 convalescent plasma expanded access programContinue

Arcturus Therapeutics and Catalent announced partnership to manufacture mRNA-Based COVID-19 vaccine
COVID-19 | Life Science History | Vaccine

Arcturus Therapeutics and Catalent announced partnership to manufacture mRNA-Based COVID-19 vaccine

On May 4, 2020, Arcturus Therapeutics and Catalent announced a partnership to support the expected manufacture of Arcturusメ…

Read More Arcturus Therapeutics and Catalent announced partnership to manufacture mRNA-Based COVID-19 vaccineContinue

AbCellera identified antibodies for potential use in drugs to treat and prevent COVID-19
Biotechnology | COVID-19 | Infectious Disease | NIH | Therapeutics

AbCellera identified antibodies for potential use in drugs to treat and prevent COVID-19

On May 3, 2020, AbCellera announced it had received a commitment of up to $175.6 million in support…

Read More AbCellera identified antibodies for potential use in drugs to treat and prevent COVID-19Continue

Gilead announced investigational antiviral remdesivir received FDA Emergency Use Authorization for treatment of COVID-19
COVID-19 | FDA | Therapeutics

Gilead announced investigational antiviral remdesivir received FDA Emergency Use Authorization for treatment of COVID-19

On May 1, 2020, Gilead announced the FDA granted emergency use authorization (EUA) for the investigational antiviral remdesivir…

Read More Gilead announced investigational antiviral remdesivir received FDA Emergency Use Authorization for treatment of COVID-19Continue

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