International Journal For Multidisciplinary Research

E-ISSN: 2582-2160     Impact Factor: 9.24

A Widely Indexed Open Access Peer Reviewed Multidisciplinary Bi-monthly Scholarly International Journal

Call for Paper Volume 6 Issue 6 November-December 2024 Submit your research before last 3 days of December to publish your research paper in the issue of November-December.

Capivasertib:the Breakthrough Cancer Treatment of the Decade's

Author(s) Gaikwad Dipti Ramesh, Dube Shubhada B., Kawade Rajendra M
Country India
Abstract Capivasertib (TRUQAP), a novel oral AKT inhibitor, targets the PI3K/AKT/mTOR pathway to overcome tumour resistance in advanced breast cancer.Capivasertib has a unique pyrrolopyrimidine derivative structure and is a highly strong ATP-competitive inhibitor of all three AKT isoforms (AKT1, AKT2, and AKT3).This article provides a thorough examination of capivasertib's synthesis, mechanisms of action, physical and chemical properties, and preclinical and clinical efficacy.Its advantages over existing treatments, possible adverse effects, and prospective use in combination therapy are examined.We also examine possible future paths for managing resistance, optimising the therapeutic advantages of capivasertib, and selecting the best patients using biomarkers.Preclinical research has demonstrated the potential of capivasertib in conjunction with endocrine therapy and anti-HER2 drugs. Its clinical importance is highlighted by the FDA's recent approval of TRUQAP in conjunction with Faslodex in November 2023 for advanced HR-positive and HER2-negative breast cancer.
Keywords Capivasertib, AKT Inhibitor, Breast cancer, TRUQAP
Field Medical / Pharmacy
Published In Volume 6, Issue 6, November-December 2024
Published On 2024-12-07
Cite This Capivasertib:the Breakthrough Cancer Treatment of the Decade's - Gaikwad Dipti Ramesh, Dube Shubhada B., Kawade Rajendra M - IJFMR Volume 6, Issue 6, November-December 2024. DOI 10.36948/ijfmr.2024.v06i06.31595
DOI https://doi.org/10.36948/ijfmr.2024.v06i06.31595
Short DOI https://doi.org/g8t3kz

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