Sirius Genomics

www.siriusgenomics.com

Sirius Genomics is a private biotechnology company based in Vancouver, British Columbia. By correlating genes to phenotypes, we are developing DNA-based diagnostic (Dx) and pharmacogenetic (PGx) tests for critical care.

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MELINTA THERAPEUTICS PARTNERS WITH BARDA TO ADVANCE TWO FDA-APPROVED ANTIBIOTICS FOR USE IN PEDIATRIC PATIENTS

Businesswire | July 11, 2023

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Melinta Therapeutics, LLC a commercial-stage company providing innovative therapies for acute and life-threatening illnesses, announced today a partnership with the Biomedical Advanced Research and Development Authority (BARDA) to advance two antibiotics currently FDA-approved for adults, BAXDELA® (delafloxacin) and VABOMERE® (meropenem and vaborbactam), for use in pediatrics. In addition, Melinta and BARDA will partner on the development of BAXDELA® against biothreat pathogens...

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MedTech

ENTOS AND BIOMARIN ENTER INTO AGREEMENT FOR PRODUCT CANDIDATES INCORPORATING ENTOS' FUSOGENIX DRUG DELIVERY PLATFORM

Entos Pharmaceuticals, Inc., BioMarin | November 16, 2021

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Entos Pharmaceuticals, Inc. (Entos), a clinical-stage biotechnology company developing genetic medicines with its Fusogenix proteolipid vehicle (PLV) nucleic acid delivery platform, and BioMarin Pharmaceutical Inc. (Nasdaq: BMRN) today announced that they have entered into an agreement that will see Entos apply its Fusogenix nucleic acid delivery technology to promising gene therapy candidates in the BioMarin pipeline. Under the agreement, Entos will create specially formulated product candidate...

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AXCELLA ANNOUNCES FDA IND CLEARANCE FOR AXA1125

Axcella | February 16, 2023

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On February 15, 2023, Axcella Therapeutics, a clinical-stage biotechnology firm that develops innovative approaches to complex diseases using multi-targeted endogenous metabolic modulator (EMM) compositions, announced that the U.S. Food and Drug Administration (FDA) has cleared its Investigational New Drug (IND) application to initiate a phase 2b/3 trial in the United States for AXA1125 for the treatment of Long COVID Fatigue. The company stated that it has obtained FDA regulato...

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BioSpace | March 20, 2020

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Adaptive Biotechnologies Corp. (Nasdaq: ADPT) and Microsoft Corp. (Nasdaq: MSFT) on Friday announced they will leverage their existing partnership mapping population-wide adaptive immune responses to diseases at scale to study COVID-19. Finding the relevant immune response signature may advance solutions to diagnose, treat and prevent the disease, augmenting existing research efforts that primarily focus on the biology of the virus. These data will be made freely available to any researcher, pub...

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Medical

MELINTA THERAPEUTICS PARTNERS WITH BARDA TO ADVANCE TWO FDA-APPROVED ANTIBIOTICS FOR USE IN PEDIATRIC PATIENTS

Businesswire | July 11, 2023

Melinta Therapeutics, LLC a commercial-stage company providing innovative therapies for acute and life-threatening illnesses, announced today a partnership with the Biomedical Advanced Research and Development Authority (BARDA) to advance two antibiotics currently FDA-approved for adults, BAXDELA® (delafloxacin) and VABOMERE® (meropenem and vaborbactam), for use in pediatrics. In addition, Melinta and BARDA will partner on the development of BAXDELA® against biothreat pathogens...

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news image

MedTech

ENTOS AND BIOMARIN ENTER INTO AGREEMENT FOR PRODUCT CANDIDATES INCORPORATING ENTOS' FUSOGENIX DRUG DELIVERY PLATFORM

Entos Pharmaceuticals, Inc., BioMarin | November 16, 2021

Entos Pharmaceuticals, Inc. (Entos), a clinical-stage biotechnology company developing genetic medicines with its Fusogenix proteolipid vehicle (PLV) nucleic acid delivery platform, and BioMarin Pharmaceutical Inc. (Nasdaq: BMRN) today announced that they have entered into an agreement that will see Entos apply its Fusogenix nucleic acid delivery technology to promising gene therapy candidates in the BioMarin pipeline. Under the agreement, Entos will create specially formulated product candidate...

Read More
news image

Cell and Gene Therapy, Industrial Impact

AXCELLA ANNOUNCES FDA IND CLEARANCE FOR AXA1125

Axcella | February 16, 2023

On February 15, 2023, Axcella Therapeutics, a clinical-stage biotechnology firm that develops innovative approaches to complex diseases using multi-targeted endogenous metabolic modulator (EMM) compositions, announced that the U.S. Food and Drug Administration (FDA) has cleared its Investigational New Drug (IND) application to initiate a phase 2b/3 trial in the United States for AXA1125 for the treatment of Long COVID Fatigue. The company stated that it has obtained FDA regulato...

Read More
news image

ADAPTIVE BIOTECHNOLOGIES AND MICROSOFT EXPAND PARTNERSHIP TO DECODE COVID-19 IMMUNE RESPONSE AND PROVIDE OPEN DATA ACCESS

BioSpace | March 20, 2020

Adaptive Biotechnologies Corp. (Nasdaq: ADPT) and Microsoft Corp. (Nasdaq: MSFT) on Friday announced they will leverage their existing partnership mapping population-wide adaptive immune responses to diseases at scale to study COVID-19. Finding the relevant immune response signature may advance solutions to diagnose, treat and prevent the disease, augmenting existing research efforts that primarily focus on the biology of the virus. These data will be made freely available to any researcher, pub...

Read More

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