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Home / SARS - Page 13

SARS

Luminex submitted joint SARS-CoV-2 and Flu/RSV respiratory panel to FDA for Emergency Use Authorization
Biotechnology | COVID-19 | FDA | Infectious Disease | Vaccine

Luminex submitted joint SARS-CoV-2 and Flu/RSV respiratory panel to FDA for Emergency Use Authorization

On Mar. 10, 2021, Luminex announced that it had submitted an Emergency Use Authorization application to the U.S….

Read More Luminex submitted joint SARS-CoV-2 and Flu/RSV respiratory panel to FDA for Emergency Use AuthorizationContinue

ImmunityBio and NantKwest began dosing participants in global trials for novel COVID-19 vaccine
COVID-19 | Life Science History | Vaccine

ImmunityBio and NantKwest began dosing participants in global trials for novel COVID-19 vaccine

On Mar. 8, 2021, ImmunityBio and NantKwest announced that the first cohorts of their South Africa and U.S….

Read More ImmunityBio and NantKwest began dosing participants in global trials for novel COVID-19 vaccineContinue

Abbott’s received FDA EUA for laboratory PCR assay that detects and differentiates SARS-CoV-2, Flu A, Flu B and RSV
Biotechnology | Diagnostics | FDA | Infectious Disease | Influenza

Abbott’s received FDA EUA for laboratory PCR assay that detects and differentiates SARS-CoV-2, Flu A, Flu B and RSV

On Mar. 5, 2021, Abbott announced the U.S. Food and Drug Administration’s (FDA) Emergency Use Authorization (EUA) for…

Read More Abbott’s received FDA EUA for laboratory PCR assay that detects and differentiates SARS-CoV-2, Flu A, Flu B and RSVContinue

Ridgeback Biotherapeutics and Merck announced preliminary findings from phase 2a trial of investigational COVID-19 therapeutic
Life Science History

Ridgeback Biotherapeutics and Merck announced preliminary findings from phase 2a trial of investigational COVID-19 therapeutic

On Mar. 5, 2021, Merck and Ridgeback Biotherapeutics, announced preliminary results from Ridgebackメs Phase 2a randomized, double-blind, placebo-controlled…

Read More Ridgeback Biotherapeutics and Merck announced preliminary findings from phase 2a trial of investigational COVID-19 therapeuticContinue

FDA issued authorization for first molecular non-prescription, at-home test
COVID-19 | Life Science History

FDA issued authorization for first molecular non-prescription, at-home test

On Mar. 5, 2021, the U.S. Food and Drug Administration issued an emergency use authorization (EUA) for the…

Read More FDA issued authorization for first molecular non-prescription, at-home testContinue

Recruitment and enrollment began for Innovation Pharma’s phase 2 clinical trial of Brilacidin for COVID-19
Biotechnology | COVID-19 | Pharmaceutical | Therapeutics

Recruitment and enrollment began for Innovation Pharma’s phase 2 clinical trial of Brilacidin for COVID-19

On Mar. 5, 2021, Innovation Pharmaceuticals reported that eight sites were participating in the Company’s international Phase 2…

Read More Recruitment and enrollment began for Innovation Pharma’s phase 2 clinical trial of Brilacidin for COVID-19Continue

Luminex received FDA Emergency Use Authorization and CE Mark for expanded NxTAG panel test Including SARS-CoV-2
Biotechnology | Disease | FDA

Luminex received FDA Emergency Use Authorization and CE Mark for expanded NxTAG panel test Including SARS-CoV-2

On Mar. 4, 2021, Luminex announced that it had received Emergency Use Authorization (EUA) from the U.S. Food…

Read More Luminex received FDA Emergency Use Authorization and CE Mark for expanded NxTAG panel test Including SARS-CoV-2Continue

Resverlogix published evidence of apabetalone’s beneficial effects on COVID-19
Biotechnology | COVID-19 | FDA

Resverlogix published evidence of apabetalone’s beneficial effects on COVID-19

On Mar. 3, 2021, Resverlogix and QIMR Berghofer Medical Research Institute announced the publishing of an article providing…

Read More Resverlogix published evidence of apabetalone’s beneficial effects on COVID-19Continue

NIH halted trial of COVID-19 convalescent plasma in emergency department patients with mild symptoms
COVID-19 | Life Science History | NIH

NIH halted trial of COVID-19 convalescent plasma in emergency department patients with mild symptoms

On Mar. 2, 2021, the NIH halted a clinical trial evaluating the safety and effectiveness of COVID-19 convalescent…

Read More NIH halted trial of COVID-19 convalescent plasma in emergency department patients with mild symptomsContinue

Merck announced partnership to produce Johnson & Johnson’s COVID-19 vaccine
Biotechnology | COVID-19 | Infectious Disease | Medicine | Vaccine

Merck announced partnership to produce Johnson & Johnson’s COVID-19 vaccine

On Mar. 2, 2021, Merck announced multiple agreements to support efforts to expand manufacturing capacity and supply of…

Read More Merck announced partnership to produce Johnson & Johnson’s COVID-19 vaccineContinue

NIH launched effort to understand MIS-C, range of SARS-CoV-2 effects on children
COVID-19 | Life Science History | NIH

NIH launched effort to understand MIS-C, range of SARS-CoV-2 effects on children

On Mar. 2, 2021, the NIH announced that it had launched a research effort to understand how SARS-CoV-2,…

Read More NIH launched effort to understand MIS-C, range of SARS-CoV-2 effects on childrenContinue

MediciNova announced it had discontinued development of a SARS-CoV-2 vaccine for COVID-19
COVID-19 | Life Science History | Vaccine

MediciNova announced it had discontinued development of a SARS-CoV-2 vaccine for COVID-19

On Mar. 2, 2021, MediciNova announced it that given the COVID-19 vaccines currently in use and other vaccines…

Read More MediciNova announced it had discontinued development of a SARS-CoV-2 vaccine for COVID-19Continue

Innovation Pharma announced publication in Journal Viruses on the anti-SARS-CoV-2 properties of brilacidin
COVID-19 | Life Science History

Innovation Pharma announced publication in Journal Viruses on the anti-SARS-CoV-2 properties of brilacidin

On Mar. 2, 2021, Innovation Pharmaceuticals reported that eight sites were participating in the Companyメs international Phase 2…

Read More Innovation Pharma announced publication in Journal Viruses on the anti-SARS-CoV-2 properties of brilacidinContinue

Quidel received Emergency Use Authorization for QuickVue at-home COVID-19 test
Biotechnology | COVID-19 | FDA

Quidel received Emergency Use Authorization for QuickVue at-home COVID-19 test

On Mar. 1, 2021, Quidel announced that it had received an Emergency Use Authorization (EUA) from the FDA,…

Read More Quidel received Emergency Use Authorization for QuickVue at-home COVID-19 testContinue

Roche SARS-CoV-2 rapid rntigen test received special approval for at-home patient self-testing in Germany
Life Science History

Roche SARS-CoV-2 rapid rntigen test received special approval for at-home patient self-testing in Germany

On Feb. 26, 2021, Roche announced it had been granted special approval by the German Federal Institute for…

Read More Roche SARS-CoV-2 rapid rntigen test received special approval for at-home patient self-testing in GermanyContinue

Pfizer and BioNTech initiated sudy to evaluate COVID-19 booster and new vaccine variants
COVID-19 | Life Science History | Vaccine

Pfizer and BioNTech initiated sudy to evaluate COVID-19 booster and new vaccine variants

On Feb. 25, 2021, Pfizer and BioNTech announced they had begun an evaluation of the safety and immunogenicity…

Read More Pfizer and BioNTech initiated sudy to evaluate COVID-19 booster and new vaccine variantsContinue

XPhyto placed first order for 25-minute COVID-19 RT-PCR tests
COVID-19 | Life Science History

XPhyto placed first order for 25-minute COVID-19 RT-PCR tests

On Feb. 24, 2021, XPhyto announced that it has placed the first order for its rapid point-of-care SARS-CoV-2…

Read More XPhyto placed first order for 25-minute COVID-19 RT-PCR testsContinue

Quest Diagnostics introduced new COVID-19 semi-quantitative serology test service
COVID-19 | Life Science History

Quest Diagnostics introduced new COVID-19 semi-quantitative serology test service

On Feb. 24, 2021, Quest Diagnostics introduced a new COVID-19 testing service that aids in providing insight into…

Read More Quest Diagnostics introduced new COVID-19 semi-quantitative serology test serviceContinue

PerkinElmer changed COVID-19 rapid testing with highly sensitive point of care antigen test for mass screening
COVID-19 | Life Science History

PerkinElmer changed COVID-19 rapid testing with highly sensitive point of care antigen test for mass screening

On Feb. 23, 2021, PerkinElmer announced the launch of the PerkinElmerᆴ COVID-19 Antigen Test for the qualitative detection…

Read More PerkinElmer changed COVID-19 rapid testing with highly sensitive point of care antigen test for mass screeningContinue

Biohaven’s multimodal antibody therapy demonstrated effective neutralization of multiple strains of COVID-19
COVID-19 | Life Science History

Biohaven’s multimodal antibody therapy demonstrated effective neutralization of multiple strains of COVID-19

On Feb. 22, 2021, Biohaven Pharmaceutical announced that a hyperimmune globulin mimic (HGM) developed with Biohaven’s proprietary MATE…

Read More Biohaven’s multimodal antibody therapy demonstrated effective neutralization of multiple strains of COVID-19Continue

BD announced collaboration for at-home rapid test for COVID-19
Diagnostics | Life Science History

BD announced collaboration for at-home rapid test for COVID-19

On Feb. 22, 2021, BD (Becton, Dickinson) and Scanwell Health, a leader in smartphone-enabled at-home medical tests, announced…

Read More BD announced collaboration for at-home rapid test for COVID-19Continue

Luminex received BARDA funding to support development and validation of test combining SARS-CoV-2 and Flu/RSV respiratory pane
Biotechnology | COVID-19 | FDA | Infectious Disease | Influenza | Therapeutics

Luminex received BARDA funding to support development and validation of test combining SARS-CoV-2 and Flu/RSV respiratory pane

On Feb. 19, 2021, Luminex announced that it had received $11.3 million in funding from the Biomedical Advanced…

Read More Luminex received BARDA funding to support development and validation of test combining SARS-CoV-2 and Flu/RSV respiratory paneContinue

Agilent announced immunoassay kit to detect SARS-CoV-2 antibodies
FDA | Life Science History

Agilent announced immunoassay kit to detect SARS-CoV-2 antibodies

On Feb. 18, 2021, Agilent Technologies announced the launch of the Agilent Dako SARS-CoV-2 IgG Enzyme-Linked Immunosorbent Assay…

Read More Agilent announced immunoassay kit to detect SARS-CoV-2 antibodiesContinue

Pacific Biosciences Sequel II Systems deployed to scale-up global viral surveillance initiatives focused on COVID-19
CDC | Genomics | Life Science History

Pacific Biosciences Sequel II Systems deployed to scale-up global viral surveillance initiatives focused on COVID-19

On Feb. 18, 2021, Pacific Biosciences announced that Labcorp had increased its commitment to highly accurate HiFi sequencing…

Read More Pacific Biosciences Sequel II Systems deployed to scale-up global viral surveillance initiatives focused on COVID-19Continue

Study published in NEJM demonstrated Pfizer-BioNTech COVID-19 vaccine neutralize South African variant spike mutations
Biotechnology | COVID-19 | Diagnostics | Infectious Disease | Therapeutics | Vaccine

Study published in NEJM demonstrated Pfizer-BioNTech COVID-19 vaccine neutralize South African variant spike mutations

On Feb. 17, 2021, BioNTech announced results from an in vitro study that provided additional data on the…

Read More Study published in NEJM demonstrated Pfizer-BioNTech COVID-19 vaccine neutralize South African variant spike mutationsContinue

XPhyto announced completion of European CE-IVD application for 25-Minute COVID-19 RT-PCR test
COVID-19 | Life Science History

XPhyto announced completion of European CE-IVD application for 25-Minute COVID-19 RT-PCR test

On Feb. 16, 2021, XPhyto and 3a-diagnostics announced that all actions and procedures required for its European regulatory…

Read More XPhyto announced completion of European CE-IVD application for 25-Minute COVID-19 RT-PCR testContinue

Meridian provided an update on the Revogeneᆴ SARS-CoV-2 EUA submission
FDA | Life Science History

Meridian provided an update on the Revogeneᆴ SARS-CoV-2 EUA submission

On Feb. 16, 2021, Meridian Bioscience provided an update on its application for Emergency Use Authorization (EUA) with…

Read More Meridian provided an update on the Revogeneᆴ SARS-CoV-2 EUA submissionContinue

BD announced EUA, CE Mark for combination molecular diagnostic to detect SARS-CoV-2, influenza A+B in single test
COVID-19 | Diagnostics | FDA | Medical Device

BD announced EUA, CE Mark for combination molecular diagnostic to detect SARS-CoV-2, influenza A+B in single test

On Feb. 12, 2021, BD (Becton, Dickinson) announced that the U.S. Food and Drug Administration (FDA) had granted…

Read More BD announced EUA, CE Mark for combination molecular diagnostic to detect SARS-CoV-2, influenza A+B in single testContinue

DOD participated in COVID-19 antibody treatment trial
Life Science History

DOD participated in COVID-19 antibody treatment trial

On Feb. 11, 2021, the the Military Health System (MHS) announced partcipation in the AstraZeneca phase III clinical…

Read More DOD participated in COVID-19 antibody treatment trialContinue

Oregon mink farm cleared from SARS-CoV-2; farm quarantine lifted
Biotechnology | COVID-19 | Diagnostics | USDA | Veterinary

Oregon mink farm cleared from SARS-CoV-2; farm quarantine lifted

On Feb. 11, 2021, the Oregon Department of Agriculture (ODA) lifted the quarantine on the Oregon mink farm…

Read More Oregon mink farm cleared from SARS-CoV-2; farm quarantine liftedContinue

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