WO2023214437 - SYSTEM AND METHOD OF DELIVERING INHIBITORS FOR PREVENTING THE ENTRY OF SARS-CoV-2 AND EMERGING VARIANTS

National phase entry is expected:
Publication Number WO/2023/214437
Publication Date 09.11.2023
International Application No. PCT/IN2023/050437
International Filing Date 05.05.2023
Title **
[English] SYSTEM AND METHOD OF DELIVERING INHIBITORS FOR PREVENTING THE ENTRY OF SARS-CoV-2 AND EMERGING VARIANTS
[French] SYSTÈME ET MÉTHODE D'ADMINISTRATION D'INHIBITEURS POUR EMPÊCHER L'ENTRÉE DU SARS-COV-2 ET DE VARIANTS ÉMERGENTS
Applicants **
BORDOLOI, Binoy K. Bordoloi Nagar, Kushal Kanwar Path, Jail Road, Assam Jorhat 785001, IN
Inventors
SAINI, Kulwant S. WS 144, Woodstock, Nirvana Country, Sector-50, Haryana Gurugram 122018, IN
KUMAR, Sachin D63 IIT Guwahati Campus, Assam Guwahati 781039, IN
MAZUMDER, Priyanka Block A-8/133, P.O Kalyani, West Bengal Nadia 741235, IN
Priority Data
202231026507   06.05.2022   IN
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Quotation for National Phase entry

Country StagesTotal
China Filing1055
EPO Filing, Examination4980
Japan Filing590
South Korea Filing574
USA Filing, Examination2710
MasterCard Visa

Total: 9909

The term for entry into the National Phase has expired. This quotation is for informational purposes only

Abstract[English] The present invention discloses a composition and method for treating viral infections. The composition and method deliver inhibitors for preventing the entry of SARS-Cov-2 viral infections and the emerging variants are disclosed. The composition comprises a protease inhibitor comprising calcium salt of Tranexamic acid (Ca-TA). The protease inhibitor further comprises lithium salt of Tranexamic acid (Li-TA). The composition demonstrates efficacy in fibrin clot systems, where the Ca salt shows unexpected behavior of clot swelling, unlike TA. This inhibitor blocks the peptide or enzyme known as plasmin from interacting with fibrin (a protein) and subsequently breaking it down. TA is a safe and commonly used small molecule drug. The Ca-TA inhibitor interferes with the binding of the viral spike protein of SARS-CoV-2 to the human cell surface receptor angiotensin- converting enzyme-2 (ACE-2) to avoid infections caused by SARS-CoV-2 infections and emerging variants.[French] La présente invention divulgue une composition et une méthode de traitement d'infections virales. La composition et la méthode fournissent des inhibiteurs pour prévenir l'entrée d'infections virales du SARS-CoV-2 et les variants émergents. La composition comprend un inhibiteur de protéase comprenant un sel de calcium d'acide tranexamique (Ca-TA). L'inhibiteur de protéase comprend en outre un sel de lithium d'acide tranexamique (Li-TA). La composition démontre une efficacité dans des systèmes de caillot de fibrine, le sel de Ca présentant un comportement inattendu de gonflement de caillot, contrairement au TA. Le présent inhibiteur bloque l'interaction du peptide ou de l'enzyme, connu sous le nom de plasmine, avec la fibrine (une protéine) et sa décomposition ultérieurement. Le TA est un médicament à petites molécules sûr et couramment utilisé. L'inhibiteur de Ca-TA interfère avec la liaison de la protéine de spicule virale du SARS-CoV-2 à l'enzyme 2 de conversion d'angiotensine de récepteur de surface de cellule humaine (ACE-2) pour éviter des infections provoquées par des infections par le SARS-CoV-2 et des variants émergents.
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