WO2023031969 - A METHOD OF IMPROVING STABILITY OF IMMUNE CHECK POINT INHIBITORS

National phase entry:
Publication Number WO/2023/031969
Publication Date 09.03.2023
International Application No. PCT/IN2022/050787
International Filing Date 02.09.2022
Title **
[English] A METHOD OF IMPROVING STABILITY OF IMMUNE CHECK POINT INHIBITORS
[French] PROCÉDÉ D'AMÉLIORATION DE LA STABILITÉ D'INHIBITEURS DU POINT DE CONTRÔLE IMMUNITAIRE
Applicants **
DR. REDDY’S LABORATORIES LIMITED
Inventors
JAYARAMAN, Murali
K GOUD, Saisharan
ASHOK NANKAR, Sunil
NANATH, Maya
SIGIREDDI, Indra Kumar
AGGARWAL, Lovisha
KALIGATLA, Sireesha Goswamy
MARIKANTY, Ravi Kumar
S, Abirami
SIVALANKA, Giridhar
PENMETSA, Ravi Kiranmai
LABALA, Suman
INGALE, Mahesh
SARKAR, Puja
DESAI, Mayur Vijay
KIRAVE, Prathibha Chandrashekhar
SHINDE, Chetan Govindrao
Priority Data
202141040075   03.09.2021   IN
202241019550   31.03.2022   IN
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Quotation for National Phase entry

Country StagesTotal
China Filing, Examination, Granting2101
EPO Filing, Examination, Granting11930
Japan Filing, Examination, Granting2016
South Korea Filing, Examination, Granting1826
USA Filing, Examination, Granting4740
MasterCard Visa
Total: 22,613

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

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Abstract[English] The present invention relates to pharmaceutical formulations of antibodies and antigen-binding fragments against human programmed death receptor-1 (PD-1)/ programmed death receptor Ligand 1 (PD-Ll), and method for preparing the same. The disclosed formulations stabilizes anti-PD1/anti-PD L1 antibody from lower to higher concentrations rendering it suitable for different modes of administration (subcutaneous/intravenous).[French] La présente invention concerne des formulations pharmaceutiques d'anticorps et de fragments de liaison à l'antigène contre le récepteur 1 de mort programmée humain (PD-1)/ligand du récepteur de mort programmée 1 (PD-L1), et leur procédé de préparation. Les formulations décrites stabilisent l'anticorps anti-PD1/anti-PD-L1 depuis de faibles concentrations jusqu'à des concentrations plus élevées, ce qui les rend appropriées pour différents modes d'administration (sous-cutanée/intraveineuse).

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