Jubilant Therapeutics Inc, a patient-centric biopharmaceutical company, has collaborated with The Wistar Institute, an independent, non-profit research institution in biomedical science, to assess the ability of Peptidyl Arginine Deiminase 4 (PAD4) inhibitors to block neutrophil extracellular trap (NET) formation in the context of COVID-19 related cytokine storms, it was reported on Friday.
PAD4 is an enzyme that catalyses the conversion of arginine to citrulline in proteins including histones and has been highly expressed in NET formation. According to certain evidences, NET is likely to be connected to the severity of COVID-19, as their formation is an outcome of pro-inflammatory cytokine release syndrome (CRS) or cytokine storms, developed by the body's immune response to the SARS-CoV-2 virus.
Syed Kazmi, president and chief executive officer of Jubilant Therapeutics, said, 'We are very pleased to announce our collaboration with the renowned Wistar Institute. Even with COVID-19 vaccines on the horizon, we know its wrath will persist for some time to come and the need to reduce its death toll remains critical. Beyond COVID-19, understanding the potential of PAD4 inhibitors to address aberrant NET formation will be important due to their role in the pathogenesis of many disease states beyond viral infections.'
Biophytis secures Brazilian funding and partnerships for obesity Phase 2 trial
Phrontline Biopharma doses first patient in TJ101 Phase 1 clinical trial
Gene Solutions' mitochondrial therapy platform targeting neurological diseases secures patent
Zhimeng Biopharma's investigational drug gains Phase 2 epilepsy clinical trial approval in China
Avidity Biosciences prices upsized common stock public offering
Sanofi's SAR402663 granted FDA fast track designation for wet AMD
Endo to share PFI and PFA data at American Orthopaedic Foot & Ankle Society Annual Meeting
Diamyd Medical secures Eurasian patent for insulin-based antigen therapy in type 1 diabetes
Sobi's Biologics License Application for NASP in uncontrolled gout accepted by FDA
Hydrosome Labs announces promising fermentation breakthrough with ultrafine bubbles
Ionis receives FDA Breakthrough Therapy designation for ION582 in Angelman syndrome
AMO Pharma signs licence agreement with PHRI and Venca Research Inc to advance new study in ARVC
Saol Therapeutics receives US FDA Complete Response Letter for SL1009 (DCA) in PDCD