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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

NIH study to determine incidence of novel Coronavirus infection in US children began
Life Science History | NIH

NIH study to determine incidence of novel Coronavirus infection in US children began

On May 4, 2020, a NIH study to help determine the rate of novel coronavirus infection in children…

Read More NIH study to determine incidence of novel Coronavirus infection in US children beganContinue

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

Cerus announced FDA approval for INTERCEPT Blood System for plasma with alternate plastic disposable kits
FDA | Life Science History

Cerus announced FDA approval for INTERCEPT Blood System for plasma with alternate plastic disposable kits

On May 4, 2020, Cerus announced FDA regulatory approval for manufacture of INTERCEPT plasma with a new, alternative…

Read More Cerus announced FDA approval for INTERCEPT Blood System for plasma with alternate plastic disposable kitsContinue

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

DNA Genotek’s ORAcollect RNA kit included in EUA granted to Biocerna SARS-CoV-2 test
Biotechnology | Diagnostics | FDA | Medical Device

DNA Genotek’s ORAcollect RNA kit included in EUA granted to Biocerna SARS-CoV-2 test

On May 4, 2020, DNA Genotek, a subsidiary of OraSure Technologies, announced that its ORAcollect RNA kit (OR-100)…

Read More DNA Genotek’s ORAcollect RNA kit included in EUA granted to Biocerna SARS-CoV-2 testContinue

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

Roche’s COVID-19 antibody test received FDA Emergency Use Authorization and is available in markets accepting the CE mark
Biotechnology | FDA

Roche’s COVID-19 antibody test received FDA Emergency Use Authorization and is available in markets accepting the CE mark

On May 2, 2020, Roche announced that the FDA has issued an Emergency Use Authorization for its new…

Read More Roche’s COVID-19 antibody test received FDA Emergency Use Authorization and is available in markets accepting the CE markContinue

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

FDA issued Emergency Use Authorization for potential COVID-19 treatment
COVID-19 | FDA | Life Science History

FDA issued Emergency Use Authorization for potential COVID-19 treatment

On May 1, 2020, the FDA issued an Emergency Use Authorization (EUA) for the investigational antiviral drug remdesivir…

Read More FDA issued Emergency Use Authorization for potential COVID-19 treatmentContinue

USC study showed Alzheimer’s gene triggers early breakdowns in the blood-brain barrier, predicting cognitive decline
Biotechnology | COVID-19 | Non-Profit Research | Therapeutics

USC study showed Alzheimer’s gene triggers early breakdowns in the blood-brain barrier, predicting cognitive decline

On May 1, 2020, a University of Southern California (USC) study suggested that temporarily suppressing the body’s immune…

Read More USC study showed Alzheimer’s gene triggers early breakdowns in the blood-brain barrier, predicting cognitive declineContinue

CDC launched the National Healthcare Safety Network COVID-19 Module Data Dashboard
CDC | COVID-19 | Life Science History

CDC launched the National Healthcare Safety Network COVID-19 Module Data Dashboard

On May 1, 2020, the CDC launched the National Healthcare Safety Network (NHSN) COVID-19 Module Data Dashboard showing…

Read More CDC launched the National Healthcare Safety Network COVID-19 Module Data DashboardContinue

US Dept of Veterans Affairs participated in drug, plasma trials in fight against COVID-19
Biotechnology | COVID-19 | Non-Profit Research | Therapeutics

US Dept of Veterans Affairs participated in drug, plasma trials in fight against COVID-19

On May 1, 2020, the U.S. Dept. of Veterans Affairs (VA) announced participation in a series of clinical…

Read More US Dept of Veterans Affairs participated in drug, plasma trials in fight against COVID-19Continue

FDA approved DARZALEX FASPRO, a new subcutaneous formulation of Daratumumab in treatment of patients with Multiple Myeloma
Biotechnology | FDA | Therapeutics

FDA approved DARZALEX FASPRO, a new subcutaneous formulation of Daratumumab in treatment of patients with Multiple Myeloma

On May 1, 2020, Janssen Pharma, a Johnson & Johnson company, announced the U.S. Food and Drug Administration…

Read More FDA approved DARZALEX FASPRO, a new subcutaneous formulation of Daratumumab in treatment of patients with Multiple MyelomaContinue

CDC launched national viral genomics consortium to better map SARS-CoV-2 transmission
CDC | COVID-19 | Genomics | Life Science History

CDC launched national viral genomics consortium to better map SARS-CoV-2 transmission

On May 1, 2020, the CDC launched the SARS-CoV-2 Sequencing for Public Health Emergency Response, Epidemiology and Surveillance…

Read More CDC launched national viral genomics consortium to better map SARS-CoV-2 transmissionContinue

Moderna and Lonza announced worldwide strategic collaboration to manufacture Moderna’s Vaccine (mRNA-1273) against novel Coronavirus
Biotechnology | COVID-19 | Infectious Disease | Therapeutics | Vaccine

Moderna and Lonza announced worldwide strategic collaboration to manufacture Moderna’s Vaccine (mRNA-1273) against novel Coronavirus

On May 1, 2020, Moderna and Lonza announced a 10-year strategic collaboration agreement to enable larger scale manufacture…

Read More Moderna and Lonza announced worldwide strategic collaboration to manufacture Moderna’s Vaccine (mRNA-1273) against novel CoronavirusContinue

CHF Solutions shipped Aquadex product to COVID-19 specialty center in Minnesota
COVID-19 | Life Science History

CHF Solutions shipped Aquadex product to COVID-19 specialty center in Minnesota

On May 1, 2020, CHF Solutions announced that it has shipped Aquadex product to a specialty care center…

Read More CHF Solutions shipped Aquadex product to COVID-19 specialty center in MinnesotaContinue

3M completed sale of its drug delivery business
Life Science History

3M completed sale of its drug delivery business

On May 1, 2020, 3M announced it had completed the sale of substantially all of its drug delivery…

Read More 3M completed sale of its drug delivery businessContinue

Cancer patients face high mortality from COVID-19
COVID-19 | Life Science History

Cancer patients face high mortality from COVID-19

On May 1, 2020, people with cancer who develop COVID-19 are much more likely to die from the…

Read More Cancer patients face high mortality from COVID-19Continue

Athersys and University Hospitals Cleveland Medical Center announce activation of first clinical site for MACOVIA study for COVID-19 Induced ARDS
COVID-19 | Life Science History

Athersys and University Hospitals Cleveland Medical Center announce activation of first clinical site for MACOVIA study for COVID-19 Induced ARDS

On May 1, 2020, Athersys and University Hospitals Cleveland Medical Center (UH Cleveland) announced that UH Cleveland is…

Read More Athersys and University Hospitals Cleveland Medical Center announce activation of first clinical site for MACOVIA study for COVID-19 Induced ARDSContinue

XBiotech identified ‘super bloods’ for development of True Human COVID-19 therapy
COVID-19 | Diagnostics | Non-Profit Research | Therapeutics

XBiotech identified ‘super bloods’ for development of True Human COVID-19 therapy

On May 1, 2020, XBiotech announced that human immune donors had been identified that can support the Company’s…

Read More XBiotech identified ‘super bloods’ for development of True Human COVID-19 therapyContinue

Medigen Vaccine Biologics SARS-CoV-2 qPCR kit obtained CE Marking and Taiwan MOHW’s approval of specific medical device’s manufacturing
Biotechnology | CDC

Medigen Vaccine Biologics SARS-CoV-2 qPCR kit obtained CE Marking and Taiwan MOHW’s approval of specific medical device’s manufacturing

On Apr. 30, 2020, Medigen Vaccine Biologics (MVB) received notice that its SARS-CoV-2 qPCR Kit had complied with…

Read More Medigen Vaccine Biologics SARS-CoV-2 qPCR kit obtained CE Marking and Taiwan MOHW’s approval of specific medical device’s manufacturingContinue

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