Tumor type | Coformulated drug(S) | Mode of administration | Clinical trial | Remark | References |
---|---|---|---|---|---|
Metastatic breast cancer | Trastuzumab | IV infusion | Phase II human study | Prolonged progression time with minimal toxicities | Esteva et al. (2002) |
HER2 positive metastatic breast cancer | Trastuzumab | Intravenous infusion | Phase II human trials | Greater efficacy with minimal toxicity | Marty et al. (2005) |
Prostate cancer | ABT 627 | Intravenous infusion | Preclinical studies (in vivo and in vitro) | ABT 627 enhances sensitivity of tumor cells to docetaxel, hence enhancing docetaxel induced growth inhibition | Banerjee et al. (2007) |
HER2 negative metastatic breast cancer | Bevacizumab | IV infusion | Phase III trials | Enhanced progression free survival with limited increase in toxicity | Miles et al. (2010) |
HER2 Metastatic breast cancer | Pertuzumab and trastuzumab | IV infusion | Phase II human study | Prolonged survival with no disease progression when compared with trastuzumab/docetaxel only | Baselga et al. (2012) |
Refractory tumors | Ritonavir | Oral | Phase II clinical trial | Comparable efficacy of combined drug in capsule and DTX/RTV separately | Moes et al. (2013) |
Metastatic breast cancer | Capecitabine | Intravenous | Phase 1II human trials | Prolonged progression time with combination when compared with docetaxel alone | Glück et al. (2013) |
Metastatic triple negative breast cancer | Cisplatin | Intravenous infusion | Phase II clinical trials | Cisplatin/DTX more effective than capecitabine/DTX | Fan et al. (2013) |
Advanced recurrent non-small cell lung cancer | Ramucirumab | IV Infusion | Retrospective study in Human subject | Combination more effective, delays disease progression | Harada et al. (2019) |
Advanced or metastatic solid tumors | Ritonavir | Oral | Phase 1 clinical trial | 75% of subject did not experience toxic side effects. Twofold increase in Cmax when combined with RTV |