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. 2021 Jun;173:306–330. doi: 10.1016/j.addr.2021.03.018

Table 2.

FDA-approved nanomedicines in routine clinical use for breast cancer treatment.

Name/Manufacturer Nanocarrier Drug/Compound Approval Date Indication References
Doxil® (Janssen Pharmaceutica) PEGylated Liposome Doxorubicin 1995 Metastatic [30], [47], [48]
Lipodox® (Sun Pharma Global FZE) PEGylated Liposome Doxorubicin 2013 Metastatic [28]
Myocet® (Sopherion Therapeutics) Non-PEGylated Liposome Doxorubicin 2000 Metastatic [31], [32], [49]
Lipusu® (Sike Pharmaceutical Co. Ltd) Liposome Paclitaxel 2006 Non-metastatic [33], [50], [51]
Abraxane® (Celgene) Albumin Paclitaxel 2005 Metastatic [36], [37], [38], [52], [53]
Genexol-PM® (Samyang Biopharm) mPEG-PDLLA Paclitaxel 2007 Non-metastatic [39], [40], [54], [55]
Nanoxel® (Fresenius Kabi India Pvt Ltd.) NIPAM-VP Paclitaxel 2006 Metastatic [41], [42], [56]
Kadcyla® (Hoffmann-La Roche) Antibody Trastuzumab/DM1 2013 Metastatic HER2+ [44], [45], [46], [57]
2019 Early HER2+, residual disease

Poly(ethylene glycol): PEG. Poly(ethylene glycol)-poly(lactide acid): mPEG-PDLLA. N-isopropyl acrylamide: NIPAM. Vinylpyrrolidone: VP. Emtansine: DM