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Home / Blog - Page 63

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DNA from air could revolutionize the way we measure animal biodiversity
Biotechnology | Diagnostics | Disease | Environmental

DNA from air could revolutionize the way we measure animal biodiversity

On Jan. 6, 2022, two new studies published in the journal Current Biology showed that environmental DNA (eDNA)…

Read More DNA from air could revolutionize the way we measure animal biodiversityContinue

Humanigen announced target enrollment in phase 2/3 ACTIV-5/BET-B trial of Lenzilumab for treatment of COVID-19 was met
COVID-19 | Life Science History

Humanigen announced target enrollment in phase 2/3 ACTIV-5/BET-B trial of Lenzilumab for treatment of COVID-19 was met

On Jan. 5, 2021, Humanigen announced that target enrollment in the Phase 2/3 ACTIV-5/BET-B study had been achieved….

Read More Humanigen announced target enrollment in phase 2/3 ACTIV-5/BET-B trial of Lenzilumab for treatment of COVID-19 was metContinue

Pfizer and BioNTech signed global collaboration agreement to develop first mRNA-based shingles vaccine
Biotechnology | COVID-19 | Infectious Disease | Vaccine

Pfizer and BioNTech signed global collaboration agreement to develop first mRNA-based shingles vaccine

On Jan. 5, 2022, Pfizer and BioNTech announced a new research, development and commercialization collaboration to develop a…

Read More Pfizer and BioNTech signed global collaboration agreement to develop first mRNA-based shingles vaccineContinue

NRx Pharmac submited EUA Application to US FDA for ZYESAMIᆴ (aviptadil) to treat patients at risk of death from COVID-19
COVID-19 | FDA | Life Science History | NIH

NRx Pharmac submited EUA Application to US FDA for ZYESAMIᆴ (aviptadil) to treat patients at risk of death from COVID-19

On Jan 5, 2022, NRx Pharmaceuticals announced that it had submitted an application for Emergency Use Authorization (EUA)…

Read More NRx Pharmac submited EUA Application to US FDA for ZYESAMIᆴ (aviptadil) to treat patients at risk of death from COVID-19Continue

Hologic added Aptima SARS-CoV-2 assay to its Global Access Initiative in resource-limited countries
HIV | Life Science History

Hologic added Aptima SARS-CoV-2 assay to its Global Access Initiative in resource-limited countries

On Jan 5, 2022, Hologic the addition of the Aptimaᆴ SARS-CoV-2 assay to its Global Access Initiative, a…

Read More Hologic added Aptima SARS-CoV-2 assay to its Global Access Initiative in resource-limited countriesContinue

Revelar Biotherapeutics and Twist Bioscience announced RBT-0813 neutralized SARS-CoV-2 Omicron and Delta variants
Life Science History

Revelar Biotherapeutics and Twist Bioscience announced RBT-0813 neutralized SARS-CoV-2 Omicron and Delta variants

On Jan 5, 2022, Revelar Biotherapeutics and Twist Bioscience announced that RBT-0813 binded to and neutralized the Omicron…

Read More Revelar Biotherapeutics and Twist Bioscience announced RBT-0813 neutralized SARS-CoV-2 Omicron and Delta variantsContinue

Pfizer provided U.S. Government with additional 10 million treatment courses of oral therapy to help combat COVID-19
Biotechnology | COVID-19 | Infectious Disease | Therapeutics

Pfizer provided U.S. Government with additional 10 million treatment courses of oral therapy to help combat COVID-19

On Jan. 4, 2022, Pfizer announced that the U.S. government had committed to purchasing an additional 10 million…

Read More Pfizer provided U.S. Government with additional 10 million treatment courses of oral therapy to help combat COVID-19Continue

Tonix Pharma announced exclusive collaboration with Kansas State University to develop LNP-Free mRNA vaccines
Biotechnology | Infectious Disease | Nanotechnology | Vaccine

Tonix Pharma announced exclusive collaboration with Kansas State University to develop LNP-Free mRNA vaccines

On Jan. 4, 2022, Tonix Pharmaceuticals announced an exclusive option agreement and research collaboration with Kansas State University…

Read More Tonix Pharma announced exclusive collaboration with Kansas State University to develop LNP-Free mRNA vaccinesContinue

Pfizer and BioNTech received U.S. FDA EUA of COVID-19 vaccine booster for individuals 12 years of age and older
COVID-19 | FDA | Life Science History

Pfizer and BioNTech received U.S. FDA EUA of COVID-19 vaccine booster for individuals 12 years of age and older

On Jan. 3, 2022, Pfizer and BioNTech announced that the U.S. Food and Drug Administration had expanded the…

Read More Pfizer and BioNTech received U.S. FDA EUA of COVID-19 vaccine booster for individuals 12 years of age and olderContinue

Amyris and Immunitybio completed joint venture for next generation Covid-19 RNA vaccine
COVID-19 | Life Science History | Vaccine

Amyris and Immunitybio completed joint venture for next generation Covid-19 RNA vaccine

On Jan. 3, 2022, Amyris and ImmunityBio announced the completion of a previously announced joint venture agreement to…

Read More Amyris and Immunitybio completed joint venture for next generation Covid-19 RNA vaccineContinue

Lenzilumab treatment response in hospitalized COVID-19 patients correlated with C-Reactive protein levels
COVID-19 | Life Science History

Lenzilumab treatment response in hospitalized COVID-19 patients correlated with C-Reactive protein levels

On Jan. 3, 2021, Humanigen announced that a manuscript detailing the results of an analysis of CRP levels…

Read More Lenzilumab treatment response in hospitalized COVID-19 patients correlated with C-Reactive protein levelsContinue

Johnson & Johnson COVID-19 vaccine demonstrated 85 percent effectiveness against hospitalization in South Africa when Omicron was dominant
COVID-19 | Life Science History | Vaccine

Johnson & Johnson COVID-19 vaccine demonstrated 85 percent effectiveness against hospitalization in South Africa when Omicron was dominant

On Dec. 30, 2021, Johnson & Johnson announced preliminary results from the South African Phase 3b Sisonke study…

Read More Johnson & Johnson COVID-19 vaccine demonstrated 85 percent effectiveness against hospitalization in South Africa when Omicron was dominantContinue

NRx Pharma filed Breakthrough Therapy Designation request for ZYESAMIᆴ (aviptadil) in patients at risk of COVID-19 death
COVID-19 | Life Science History

NRx Pharma filed Breakthrough Therapy Designation request for ZYESAMIᆴ (aviptadil) in patients at risk of COVID-19 death

On Dec. 29, 2021, NRx Pharmaceuticals announced that it hds filed a new Breakthrough Therapy Designation (BTD) request…

Read More NRx Pharma filed Breakthrough Therapy Designation request for ZYESAMIᆴ (aviptadil) in patients at risk of COVID-19 deathContinue

U.S. DoD awarded $136.7 million to MilliporeSigma for domestic production capacity of COVID-19 point-of-care tests parts
Biotechnology | COVID-19 | Diagnostics | Medical Device

U.S. DoD awarded $136.7 million to MilliporeSigma for domestic production capacity of COVID-19 point-of-care tests parts

On Dec. 29, 2021, the Department of Defense (DoD), on behalf of and in coordination with the U.S….

Read More U.S. DoD awarded $136.7 million to MilliporeSigma for domestic production capacity of COVID-19 point-of-care tests partsContinue

Novavax and Serum Institute of India received Emergency Use Authorization for COVID-19 vaccine in India
Biotechnology | COVID-19 | Infectious Disease | Nanotechnology | Vaccine

Novavax and Serum Institute of India received Emergency Use Authorization for COVID-19 vaccine in India

On Dec. 28, 2021, Novavax and Serum Institute of India announced that the Drugs Controller General of India…

Read More Novavax and Serum Institute of India received Emergency Use Authorization for COVID-19 vaccine in IndiaContinue

COVID-19 vaccine developed by Biological E using Dynavax’s CpG 1018 adjuvant received India DCGI approval for emergency use
COVID-19 | Life Science History | Vaccine

COVID-19 vaccine developed by Biological E using Dynavax’s CpG 1018 adjuvant received India DCGI approval for emergency use

On Dec. 28, 2021, Dynavax announced that Biological E had reported that CORBEVAXル, their COVID-19 vaccine which contains…

Read More COVID-19 vaccine developed by Biological E using Dynavax’s CpG 1018 adjuvant received India DCGI approval for emergency useContinue

PacBio’s HiFiViral Surveillance Kit Performance not impacted by Omicron mutations
Biotechnology | COVID-19 | Disease | Genomics

PacBio’s HiFiViral Surveillance Kit Performance not impacted by Omicron mutations

On Dec. 28, 2021, Pacific Biosciences announced that its new HiFiViral SARS-CoV-2 solution had successfully sequenced and captured…

Read More PacBio’s HiFiViral Surveillance Kit Performance not impacted by Omicron mutationsContinue

Development of WRAI’s pan-coronavirus vaccine showed promise
COVID-19 | Infectious Disease | Non-Profit Research | Vaccine

Development of WRAI’s pan-coronavirus vaccine showed promise

On Dec. 28, 2021, researchers at the Walter Reed Army Institute of Research in Silver Spring, Maryland announced…

Read More Development of WRAI’s pan-coronavirus vaccine showed promiseContinue

Moderna announced Switzerland exercised option to purchase seven million additional doses of COVID-19 booster vaccine
Biotechnology | COVID-19 | Infectious Disease | Vaccine

Moderna announced Switzerland exercised option to purchase seven million additional doses of COVID-19 booster vaccine

On Dec. 27, 2021, Moderna announced that the Swiss Federal Government had exercised its option to purchase an…

Read More Moderna announced Switzerland exercised option to purchase seven million additional doses of COVID-19 booster vaccineContinue

Moderna announced supply agreement with South Korea for additional 20 million doses of COVID-19 vaccine
Biotechnology | COVID-19 | Infectious Disease | Vaccine

Moderna announced supply agreement with South Korea for additional 20 million doses of COVID-19 vaccine

On Dec. 27, 2021, Moderna announced a revised supply agreement with the government of South Korea for 20…

Read More Moderna announced supply agreement with South Korea for additional 20 million doses of COVID-19 vaccineContinue

Sorrento announced COVISTIX COVID-19 virus rapid antigen detection test detected the Omicron variant
Biotechnology | COVID-19 | Vaccine

Sorrento announced COVISTIX COVID-19 virus rapid antigen detection test detected the Omicron variant

On Dec. 27, 2021, Sorrento Therapeutics announced that initial testing of COVISTIX on recombinant N proteins demonstrated its…

Read More Sorrento announced COVISTIX COVID-19 virus rapid antigen detection test detected the Omicron variantContinue

FDA authorized COVID-19 Over-the-Counter test based on data from NIH Independent Test Assessment Program
COVID-19 | FDA | Life Science History

FDA authorized COVID-19 Over-the-Counter test based on data from NIH Independent Test Assessment Program

On Dec. 27, 2021, the U.S. Food and Drug Administration authorized an over-the-counter (OTC) COVID-19 antigen test, the…

Read More FDA authorized COVID-19 Over-the-Counter test based on data from NIH Independent Test Assessment ProgramContinue

COVID-19 heroes & Remembrance
Biotechnology | Cartoons - Original | COVID-19 | Diagnostics | FDA | Life Science History | Non-Profit Research | Pharmaceutical | Therapeutics | U.S. Congress | Vaccine

COVID-19 heroes & Remembrance

Our Heroes and Remembrance illustration has Maurice Ralph Hilleman and John Enders, pioneering developers of common vaccines, and…

Read More COVID-19 heroes & RemembranceContinue

Merck and Ridgeback’s molnupiravir, an investigational oral antiviral COVID-19 treatment, received special approval for emergency in Japan
Biotechnology | COVID-19 | Pharmaceutical | Therapeutics

Merck and Ridgeback’s molnupiravir, an investigational oral antiviral COVID-19 treatment, received special approval for emergency in Japan

On Dec. 24, 2021, Merck and Ridgeback Biotherapeutics announced that Japanメs Ministry of Health, Labor and Welfare had…

Read More Merck and Ridgeback’s molnupiravir, an investigational oral antiviral COVID-19 treatment, received special approval for emergency in JapanContinue

Roche COVID-19 at-home test granted FDA Emergency Use Authorization to expand access to rapid self-testing solutions in the United States
COVID-19 | Life Science History

Roche COVID-19 at-home test granted FDA Emergency Use Authorization to expand access to rapid self-testing solutions in the United States

On Dec. 24, 2021, Roche announced that the U.S. Food and Drug Administration had granted Emergency Use Authorization…

Read More Roche COVID-19 at-home test granted FDA Emergency Use Authorization to expand access to rapid self-testing solutions in the United StatesContinue

Novavax and SK bioscience announed expanded manufacturing agreement
Biotechnology | COVID-19 | Infectious Disease | Nanotechnology | Vaccine

Novavax and SK bioscience announed expanded manufacturing agreement

On Dec. 23, 2021, Novavax and SK bioscience announced the expansion of the companies’ collaboration and license agreements…

Read More Novavax and SK bioscience announed expanded manufacturing agreementContinue

Merck and Ridgeback’s molnupiravir received U.S. FDA EUA for treatment of high-risk adults with COVID-19
Biotechnology | COVID-19 | FDA | Medicine | Pharmaceutical | Therapeutics

Merck and Ridgeback’s molnupiravir received U.S. FDA EUA for treatment of high-risk adults with COVID-19

On Dec. 23, 2021, Merck and Ridgeback Biotherapeutics announced that the U.S. Food and Drug Administration (FDA) had…

Read More Merck and Ridgeback’s molnupiravir received U.S. FDA EUA for treatment of high-risk adults with COVID-19Continue

OPKO Health announced topline results from phase 2 trial evaluating RAYALDEE to treat symptomatic COVID-19 outpatients
COVID-19 | Life Science History

OPKO Health announced topline results from phase 2 trial evaluating RAYALDEE to treat symptomatic COVID-19 outpatients

On Dec. 23, 2021, OPKO announced preliminary topline results from its Phase 2 trial with RAYALDEEᆴ to treat…

Read More OPKO Health announced topline results from phase 2 trial evaluating RAYALDEE to treat symptomatic COVID-19 outpatientsContinue

Pfizer and BioNTech submit updated longer-term follow-up data of COMIRNATY in adolescents to EMA
Biotechnology | COVID-19 | Pharmaceutical | Therapeutics | Vaccine

Pfizer and BioNTech submit updated longer-term follow-up data of COMIRNATY in adolescents to EMA

On Dec. 23, 2021, Pfizer and BioNTech announced that they had submitted longer-term follow-up data from the companiesメ…

Read More Pfizer and BioNTech submit updated longer-term follow-up data of COMIRNATY in adolescents to EMAContinue

Eight substances added to 15th Report on Carcinogens
Life Science History | U.S. Congress

Eight substances added to 15th Report on Carcinogens

On Dec. 23, 2021, eight substances were added to the Report on Carcinogens, bringing the total list to…

Read More Eight substances added to 15th Report on CarcinogensContinue

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