Capivasertib

(TruQap®)

TruQap®

Drug updated on 10/21/2024

Dosage FormTablet (oral; 160 mg, 200 mg)
Drug ClassKinase inhibitors
Ongoing and
Completed Studies
ClinicalTrials.gov

Indication

  • Indicated for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative, locally advanced or metastatic breast cancer with one or more PIK3CA/AKT1/PTEN-alterations as detected by an FDA-approved test following progression on at least one endocrine-based regimen in the metastatic setting or recurrence on or within 12 months of completing adjuvant therapy.

Latest News

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Summary
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  • This summary is based on the review of one systematic review(s)/meta-analysis(es). [1]
  • In the endocrine-sensitive setting, CDK4/6 inhibitors combined with fulvestrant 500 mg (CDK4/6i+F500) had a SUCRA of 97.3% for both progression-free survival (PFS) and overall survival (OS). The hazard ratio (HR) for OS between CDK4/6i+F500 versus fulvestrant 500 mg alone was 0.77 (95% CrI 0.63-0.95).
  • In the endocrine-resistant setting, CDK4/6i+F500 showed a SUCRA of 95.7% for PFS, and capivasertib combined with fulvestrant 500 mg (capivasertib+F500) had a SUCRA of 84.7% for OS. The HR for OS between CDK4/6i+F500 and fulvestrant 500 mg alone was 0.77 (95% CrI 0.67-0.89).
  • There is no safety information available in the reviewed documents.
  • There is no population types or subgroups information available in the reviewed documents.

Product Monograph / Prescribing Information

Document TitleYearSource
TruQap (capivasertib) Prescribing Information.2023AstraZeneca Pharmaceuticals LP., Wilmington, DE

Systematic Reviews / Meta-Analyses

Clinical Practice Guidelines