Hyaluronidase/pertuzumab/trastuzumab - Roche
Alternative Names: Herceptin/perjeta; Perjeta/herceptin; Pertuzumab FDC SC; Pertuzumab/trastuzumab; Pertuzumab/trastuzumab/hyaluronidase-zzxf; Pertuzumab/trastuzumab/vorhyaluronidase alfa; PH FDC SC; Phesgo; Phesgo OBI; RG-6264; Trastuzumab/pertuzumabLatest Information Update: 14 May 2025
At a glance
- Originator Roche
- Developer Chugai Pharmaceutical; Medica Scientia Innovation Research; Merck & Co; Roche; Seagen
- Class Antineoplastics; Immunotherapies; Monoclonal antibodies
- Mechanism of Action Antibody-dependent cell cytotoxicity; Dimerisation inhibitors; Hyaluronidase replacements
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Orphan Drug Status
Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.
- New Molecular Entity No
Highest Development Phases
- Marketed Colorectal cancer; HER2 positive breast cancer
- Phase II Solid tumours
Most Recent Events
- 30 Apr 2025 European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP) issues a positive opinion for Hyaluronidase/pertuzumab/trastuzumab in European Union
- 22 Jul 2024 Phase-II clinical trials in HER2-positive-breast-cancer (Inoperable/Unresectable, Recurrent, Metastatic disease, Combination therapy) in Spain (SC) (NCT06172127)
- 27 Feb 2024 Genentech completes a phase II trial in Solid tumours (Inoperable/Unresectable, Late-stage disease, Metastatic disease) in USA (PO) (NCT04632992)