PERJETA (pertuzumab)

TherapyGenentech

PERJETA (pertuzumab) from Genentech is a HER2-directed antibody used in combination with trastuzumab-based regimens.

Approvals
3
Indications
1
Biomarkers
1
Mapped tests
3

Where this therapy is approved with a companion diagnostic

Each row represents a defined combination of indication, biomarker criteria, and PERJETA. Select a testing pathway to see the eligible companion diagnostic tests.

Indication-specific approvals

Approvals where PERJETA is tied to a specific indication and biomarker definition.

IndicationBiomarker criteriaNotes
Breast Cancer
Solid Tumor · Breast
ERBB2 (HER2)
  • gene amplification
View testing pathway →
Tumor-agnostic approvals

Approvals defined at the solid tumor level where biomarker criteria determine eligibility for PERJETA.

No tumor-agnostic companion diagnostic approvals are currently mapped for this therapy.

Tests used in these approvals

These assays are identified in FDA labeling or sponsor materials as companion diagnostics or acceptable tests when considering PERJETA for eligible patients.

Test
FoundationOne CDx
Foundation Medicine, Inc.
Method
NGS
Specimen
Tissue (FFPE)
Test
HER2 FISH pharmDx Kit
Dako Denmark A/S (Agilent Technologies, Inc.)
Method
FISH
Specimen
Tissue (FFPE)
Test
HercepTest
Dako Denmark A/S (Agilent Technologies, Inc.)
Method
IHC
Specimen
Tissue (FFPE)
This view is scoped to PERJETA (pertuzumab). You can also see how it compares with other therapies and indications on the main Know Your Companions™ map.
PERJETA (pertuzumab) | CDxTests.com | CDx Tests