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. 2019 Nov 13;11(11):1786. doi: 10.3390/cancers11111786

Table 1.

Tabular representation of drugs and their corresponding clinical trial information.

Drug Target Clinical Trial ID Number of Patients Phase Result
Birinapant IAPs NCT01681368 11 2 SD = 2 (18.2 %) upto 4-5 months
CR = 0
PR = 0
Birinapant IAPs NCT01940172 18 1 PR = 1
SD = 4
DEBIO1143 IAPs NCT01930292 11 out of 31 with ovarian cancer 1 PR = 4 (36.4%)
SD = 4 (36.4%)
PD = 3 (27.2%)
Terminated
PRIMA-1MET P53 NCT02098343 200 1 & 2 Ongoing
Alisertib Aurora kinase (PI3K/Akt/mTOR pathway) NCT01091428 191 and 142 respectively 1 & 2 median PFS increased by 2 months
Alisertib Aurora kinase (PI3K/Akt/mTOR pathway) NCT00853307 31 2 CR = 3 (10%)
PR = 4 (31%)
SD = 7 (23%)
PD = 12 (40%)
NE = 5 (16.1%)
Crizotinib MET/ALK/ROS1 NCT02465060 7/635 with MET amplification (ovarian cancer) 2 Ongoing
Crizotinib MET/ALK/ROS1 NCT02568267 300 patients with different types of cancer 2 Ongoing
Cabozantinib MET NCT00940225 70 2 PR = 14 (20%)
OS = 50% at 12 weeks
PFS= 5.9 months
Cabozantinib MET NCT02315430 13 2 Results awaited

CR = complete response, PR = partial response, SD = stable disease, PD = progressive disease, OS = overall survival, PFS = Platinum free survival, and NE = inevaluable, IAPs = inhibitor of apoptotic proteins, PI3K = phosphatidylinositol 3-kinase, mTOR = mammalian target of rapamycin, MET = mesenchymal-epithelial transition factor, ALK = anaplastic lymphoma kinase, ROS1 = ROS proto-oncogene 1.