Adagrasib

(Krazati®)

Krazati®

Drug updated on 10/24/2024

Dosage FormTablet (oral; 200 mg)
Drug ClassRAS GTPase family inhibitors
Ongoing and
Completed Studies
ClinicalTrials.gov

Indication

  • As a single agent, indicated for the treatment of adult patients with KRAS G12C-mutated locally advanced or metastatic non-small cell lung cance (NSCLC), as determined by an FDA-approved test, who have received at least one prior systemic therapy
  • In combination with cetuximab, indicated for the treatment of adult patients with KRAS G12C-mutated locally advanced or metastatic colorectal cancer (CRC), as determined by an FDA-approved test, who have received prior treatment with fluoropyrimidine-, oxaliplatin-, and irinotecanbased chemotherapy.

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Summary
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  • This summary is based on the review of two systematic review(s)/meta-analysis(es). [1-2]
  • The pooled Objective Response Rate (ORR) for KRAS(G12C) inhibitors was 28.6% (95% Confidence Interval (CI), 21.2-36.6%) and 31% (95% CI, 25-37%).
  • The pooled Disease Control Rate (DCR) was 85.5% (95% CI, 82.2-88.6%) and 86% (95% CI, 82-89%).
  • The Progression-Free Survival (PFS) rate at 6 months was 49.6% (95% CI, 41.4-57.9%) and at 12 months, 26.7% (95% CI, 19.8-34.1%).
  • The pooled analysis of treatment-related adverse events (trAEs) showed an incidence of 79.3% (95% CI, 66.2-90.0%) for any grade trAEs, with 24.4% (95% CI, 16.7-32.9%) of patients experiencing grade three or more trAEs.
  • Sotorasib was associated with significantly lower incidences of any grade trAEs (OR (Odds Ratio) = 0.07, 95% CI, 0.03-0.14) and grade three or more trAEs (OR = 0.34, 95% CI, 0.24-0.49) compared to adagrasib.
  • There is no population types or subgroups information available in the reviewed documents.

Product Monograph / Prescribing Information

Document TitleYearSource
Krazati (adagrasib) Prescribing Information.2024Bristol-Myers Squibb Company, Princeton, NJ

Systematic Reviews / Meta-Analyses