Table 2.
Name | Target | Type of study | Trial ID* |
---|---|---|---|
Individual therapy | |||
MK-0752 (Merck and Co, whitehouse Station, NJ, USA) | Metastatic or locally advanced breast cancer | Phase I | NCT00106145 |
PF03084014 (Pfizer, Groton, CT, USA) | Advanced solid tumors | Phase I | NCT00878189 |
RO-4929097 (Roche, Nutley, NJ, USA) | Advanced or metastatic breast cancer or recurrent triple negative breast cancer | Phase II | NCT01151449 |
Combination therapy | |||
MK-0752 + Docetaxel | Locally advanced or metastatic breast cancer | Phase I/II | NCT00645333 |
MK-0752 + Tamoxifen or Letrozole | Early stage breast cancer | Pilot study | NCT00756717 |
Ridaforolimus (MK-8669) with either MK-0752 or MK-2206 (Akt inhibitor) | Advanced solid tumor | Phase I | NCT01295632 |
RO-4929097 + Capecitabine | Refractory solid tumors | Phase I | NCT01158274 |
RO-4929097 + Cediranib maleate | Advanced solid tumors | Phase I clinical trial | NCT01131234 |
RO-4929097 + Letrozole | Post-menopausal ER+/PR+ Stage I or II breast cancer | Phase Ib clinical trial | NCT01208441 |
RO-4929097 + Vismodegib | Metastatic breast cancer | Phase I clinical trial | NCT01071564 |
RO-4929097 + Paclitaxel + Carboplatin | Stage II or III triple negative breast cancer | Phase I clinical trial | NCT01238133 |
Note:
clinicaltrials.gov.
Abbreviations: ER, estrogen receptor; PR, progesterone receptor.