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Bellerophon announced results of interim analysis of phase 3 COViNOX study of INOpulseᆴ for COVID-19
COVID-19 | FDA | Life Science History

Bellerophon announced results of interim analysis of phase 3 COViNOX study of INOpulseᆴ for COVID-19

On Nov. 23, 2020, Bellerophon Therapeutics announced that the independent Data Monitoring Committee (DMC) had completed its pre-specified…

Read More Bellerophon announced results of interim analysis of phase 3 COViNOX study of INOpulseᆴ for COVID-19Continue

CytoDyn reached enrollment target of 293 patients for 2nd DSMC interim analysis of phase 3 COVID-19 trial
Biotechnology | COVID-19 | Infectious Disease | Therapeutics

CytoDyn reached enrollment target of 293 patients for 2nd DSMC interim analysis of phase 3 COVID-19 trial

On Nov. 23, 2020, CytoDyn announced it had reached enrollment of 293 patients in its Phase 3 trial…

Read More CytoDyn reached enrollment target of 293 patients for 2nd DSMC interim analysis of phase 3 COVID-19 trialContinue

National Resilience launched as the worldメs most advanced biopharmaceutical manufacturing ecosystem
Life Science History

National Resilience launched as the worldメs most advanced biopharmaceutical manufacturing ecosystem

On Nov. 23, 2020, National Resilience, founded by ARCH Venture Partnersメ Robert Nelsen, launched as the worldメs most…

Read More National Resilience launched as the worldメs most advanced biopharmaceutical manufacturing ecosystemContinue

FDA authorized monoclonal antibodies for treatment of COVID-19
COVID-19 | FDA | Life Science History

FDA authorized monoclonal antibodies for treatment of COVID-19

On Nov. 21, 2020, the FDA issued an emergency use authorization (EUA) for Regeneron Pharmaceuticals’ casirivimab and imdevimab…

Read More FDA authorized monoclonal antibodies for treatment of COVID-19Continue

Regeneron’s REGEN-COV2 ntibody cocktail for COVID-19 received FDA Emergency Use Authorization
COVID-19 | FDA | Life Science History

Regeneron’s REGEN-COV2 ntibody cocktail for COVID-19 received FDA Emergency Use Authorization

On Nov. 21, 2020, Regeneron announced that the antibody cocktail casirivimab and imdevimab administered together (also known as…

Read More Regeneron’s REGEN-COV2 ntibody cocktail for COVID-19 received FDA Emergency Use AuthorizationContinue

NIH expanded research to improve COVID-19 testing among underserved and vulnerable populations
Life Science History | NIH

NIH expanded research to improve COVID-19 testing among underserved and vulnerable populations

On Nov. 20, 2020, the National Institutes of Health (NIH) awarded nearly $45 million to expand the research…

Read More NIH expanded research to improve COVID-19 testing among underserved and vulnerable populationsContinue

Avian influenza virus spread rapidly in Europe
Biotechnology | Diagnostics | Infectious Disease | Influenza | Vaccine

Avian influenza virus spread rapidly in Europe

On Nov. 20, 2020, the ‘European Food Safety Authority reported that within the past month more than 300…

Read More Avian influenza virus spread rapidly in EuropeContinue

Prior COVID-19 infection offered protection from re-infection for at least six months
COVID-19 | Life Science History

Prior COVID-19 infection offered protection from re-infection for at least six months

On Nov. 20, 2020, the University of Oxford announced a study suggested that individuals who have previously had…

Read More Prior COVID-19 infection offered protection from re-infection for at least six monthsContinue

Eiger announced FDA approval of Zokinvyル (lonafarnib) treatment for Hutchinson-Gilford Progeria Syndrome
FDA | Life Science History

Eiger announced FDA approval of Zokinvyル (lonafarnib) treatment for Hutchinson-Gilford Progeria Syndrome

On Nov. 20, 2020, Eiger BioPharmaceuticals announced that the FDA had approved ZokinvyTM (lonafarnib) for the treatment of…

Read More Eiger announced FDA approval of Zokinvyル (lonafarnib) treatment for Hutchinson-Gilford Progeria SyndromeContinue

Lilly’s neutralizing antibody bamlanivimab received interim authorization from Health Canada as treatment for COVID-19
COVID-19 | Life Science History

Lilly’s neutralizing antibody bamlanivimab received interim authorization from Health Canada as treatment for COVID-19

On Nov. 20, 2020, Eli Lilly announced that Health Canada had granted authorization under the Interim Order Respecting…

Read More Lilly’s neutralizing antibody bamlanivimab received interim authorization from Health Canada as treatment for COVID-19Continue

Aptima HIV-1 Quant Dx assay receivds additional FDA approval for use as aAid in diagnosis of HIV infection
FDA | HIV | Life Science History

Aptima HIV-1 Quant Dx assay receivds additional FDA approval for use as aAid in diagnosis of HIV infection

On Nov. 30, 2020, Hologic announced that the FDA had approved a diagnostic claim for its HIV-1 (human…

Read More Aptima HIV-1 Quant Dx assay receivds additional FDA approval for use as aAid in diagnosis of HIV infectionContinue

Broad Institute rapid COVID-19 test delivered accurate results with minimal equipment
COVID-19 | Life Science History

Broad Institute rapid COVID-19 test delivered accurate results with minimal equipment

On Nov. 20, 2020, researchers at the Broad Institute of MIT and Harvard announced they had developed a…

Read More Broad Institute rapid COVID-19 test delivered accurate results with minimal equipmentContinue

Pfizer and BioNTech to submit Emergency Use Authorization Request to the FDA for COVID-19 vaccine
FDA | Life Science History

Pfizer and BioNTech to submit Emergency Use Authorization Request to the FDA for COVID-19 vaccine

On Nov. 20, 2020, Pfizer and BioNTech announced they submitted a request to the Food and Drug Administration…

Read More Pfizer and BioNTech to submit Emergency Use Authorization Request to the FDA for COVID-19 vaccineContinue

Study of ‘exceptional responders’ yields clues to cancer and potential treatments
Biotechnology | NIH | Therapeutics

Study of ‘exceptional responders’ yields clues to cancer and potential treatments

On Nov. 19, 2020, in a comprehensive analysis of patients with cancer who had exceptional responses to therapy,…

Read More Study of ‘exceptional responders’ yields clues to cancer and potential treatmentsContinue

FX06 clinical trial for treatment of most severely affected patients with COVID-19 begun in France
COVID-19 | Life Science History

FX06 clinical trial for treatment of most severely affected patients with COVID-19 begun in France

On Nov. 19, 2020, F4 Pharma announced the inclusion of the first patient with severe COVID-19 in a…

Read More FX06 clinical trial for treatment of most severely affected patients with COVID-19 begun in FranceContinue

Oxford Coronavirus vaccine produced strong immune response in older adults
COVID-19 | Life Science History | Vaccine

Oxford Coronavirus vaccine produced strong immune response in older adults

On Nov. 19, 2020, the University of Oxford announced that the ChAdOx1 nCov-2019 coronavirus vaccine had been shown…

Read More Oxford Coronavirus vaccine produced strong immune response in older adultsContinue

Viruses shown to evolve as a result of different immune responses in different ethnic populations
Biotechnology | COVID-19 | Diagnostics | HIV

Viruses shown to evolve as a result of different immune responses in different ethnic populations

On Nov. 19, 2020, University of Oxford researchers announced that research into the HIV-1 virus had shed light…

Read More Viruses shown to evolve as a result of different immune responses in different ethnic populationsContinue

Novartis secured exclusive rights for potential acute respiratory distress syndrome cell therapy
Biotechnology | COVID-19 | Therapeutics

Novartis secured exclusive rights for potential acute respiratory distress syndrome cell therapy

On Nov. 19, 2020, Novartis announced that it had entered into an exclusive worldwide license and collaboration agreement…

Read More Novartis secured exclusive rights for potential acute respiratory distress syndrome cell therapyContinue

Medigen Vaccines announced publication of positive results from preclinical studies of COVID-19 vaccine candidate
Biotechnology | COVID-19 | Therapeutics | Vaccine

Medigen Vaccines announced publication of positive results from preclinical studies of COVID-19 vaccine candidate

On Nov. 19, 2020, Medigen Vaccine Biologics announced that preclinical results of their COVID-19 vaccine candidate had been…

Read More Medigen Vaccines announced publication of positive results from preclinical studies of COVID-19 vaccine candidateContinue

Cue’s Molecular, point-of-care COVID-19 tests deployed to five states in HHS and DOD pilot program
Biotechnology | COVID-19 | Diagnostics | Infectious Disease | Medical Device

Cue’s Molecular, point-of-care COVID-19 tests deployed to five states in HHS and DOD pilot program

On Nov. 19, 2020, Cue Health announced that, as of November 9, the U.S. Department of Health and…

Read More Cue’s Molecular, point-of-care COVID-19 tests deployed to five states in HHS and DOD pilot programContinue

ApiJect approved for $590 million loan from US International DFC to build drug manufacturing facility in North Carolina
COVID-19 | Life Science History | Vaccine

ApiJect approved for $590 million loan from US International DFC to build drug manufacturing facility in North Carolina

On Nov. 19, 2020, ApiJect Systems, a public benefit corporatio, announced that it had been approved by the…

Read More ApiJect approved for $590 million loan from US International DFC to build drug manufacturing facility in North CarolinaContinue

Baricitinib received Emergency Use Authorization from FDA for treatment of hospitalized patients with COVID-19
Biotechnology | COVID-19 | FDA | Therapeutics

Baricitinib received Emergency Use Authorization from FDA for treatment of hospitalized patients with COVID-19

On Nov. 19, 2020, Eli Lilly and Incyte announced that the FDA had issued an Emergency Use Authorization…

Read More Baricitinib received Emergency Use Authorization from FDA for treatment of hospitalized patients with COVID-19Continue

XBiotech data showed effective anti-virus activity for antibodies in candidate influenza-COVID-19 therapeutic
Biotechnology | COVID-19 | Diagnostics | Infectious Disease | Influenza | Therapeutics

XBiotech data showed effective anti-virus activity for antibodies in candidate influenza-COVID-19 therapeutic

On Nov. 19, 2020, XBiotech announced data for its breakthrough candidate therapy for treating infections of influenza and…

Read More XBiotech data showed effective anti-virus activity for antibodies in candidate influenza-COVID-19 therapeuticContinue

Texas A&M System, Worlds Inc. collaborated on COVID-19 breathalyzer
Biotechnology | COVID-19 | Diagnostics | Infectious Disease | Medical Device

Texas A&M System, Worlds Inc. collaborated on COVID-19 breathalyzer

On Nov. 19, 2020, Dallas-based company, Worlds Inc., the U.S. Air Force and Texas A&M University announced a…

Read More Texas A&M System, Worlds Inc. collaborated on COVID-19 breathalyzerContinue

11th Ebola outbreak in the Democratic Republic of the Congo declared over
Disease | WHO

11th Ebola outbreak in the Democratic Republic of the Congo declared over

On Nov. 18, 2020, marked the end of the 11th Ebola outbreak in the Democratic Republic of the…

Read More 11th Ebola outbreak in the Democratic Republic of the Congo declared overContinue

BioVersys announced first subjects dosed in phase 1 clinical trial of BV100
Life Science History

BioVersys announced first subjects dosed in phase 1 clinical trial of BV100

On Nov. 18, 2020, BioVersys announced a milestone by entering clinical development with the start of Phase 1…

Read More BioVersys announced first subjects dosed in phase 1 clinical trial of BV100Continue

Relief Therapeutics selected CRO and CDMO for RLF-100TM in Europe
COVID-19 | Life Science History

Relief Therapeutics selected CRO and CDMO for RLF-100TM in Europe

On Nov. 18, 2020, RELIEF THERAPEUTICS announced the appointment of Syneos Healthᆴ, a leading global clinical research organization…

Read More Relief Therapeutics selected CRO and CDMO for RLF-100TM in EuropeContinue

Gilead announced long-acting HIV-1 capsid inhibitor, lenacapavir, achieved primary endpoint in phase 2/3 study
Biotechnology | HIV | Therapeutics

Gilead announced long-acting HIV-1 capsid inhibitor, lenacapavir, achieved primary endpoint in phase 2/3 study

On Nov. 18, 2020, Gilead Sciences announced topline results from the Phase 2/3 CAPELLA trial evaluating the company’s…

Read More Gilead announced long-acting HIV-1 capsid inhibitor, lenacapavir, achieved primary endpoint in phase 2/3 studyContinue

Pfizer and BioNTech announced phase 3 study of COVID-19 vaccine candidate met all efficacy endpoints
COVID-19 | Life Science History | Vaccine

Pfizer and BioNTech announced phase 3 study of COVID-19 vaccine candidate met all efficacy endpoints

On Nov. 18, 2020, Pfizer and BioNTech announced that, after conducting the final efficacy analysis in their ongoing…

Read More Pfizer and BioNTech announced phase 3 study of COVID-19 vaccine candidate met all efficacy endpointsContinue

Todos Medical announced positive initial clinical proof-of-concept data for rapid SARS-CoV-2 3CL protease detection assay
COVID-19 | FDA | Life Science History

Todos Medical announced positive initial clinical proof-of-concept data for rapid SARS-CoV-2 3CL protease detection assay

On Nov. 18, 2020, Todos Medical announced positive clinical proof of concept data from its lab-based rapid SARS-CoV-2…

Read More Todos Medical announced positive initial clinical proof-of-concept data for rapid SARS-CoV-2 3CL protease detection assayContinue

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