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. 2024 Mar 1;13:26. doi: 10.1186/s40164-024-00493-8

Table 8.

Clinical trials of PDC drugs for lung cancer treatment

PDC drug name Target NCT number Status Study phase Actual enrollment Primary endpoint Start date
ZL-2306 PARP NCT03516084 Terminated III 185 PFS Aug 2018
CYH33 STAT3 NCT04586335 Recruiting I 350 ORR Sep 2020
CYH33 STAT3 NCT03544905 Recruiting I 100 MTD Jul 2018
MEDI9197 IL-17RA NCT02556463 Terminated I 53 MTD Oct 2018
BT-1718 STn NCT03486730 Not recruiting I/II 72 MTD Jan 2018
GRN1005 LPR1 NCT01679743 Withdrawn II 20 Not provided Aug 2012
GRN1005 LPR1 NCT01497665 Terminated II 16 ORR Jan 2013
GRN1005 LPR1 NCT00539383

Completed

(NA)

I 56 MTD Mar 2010
BT-5528 CD13 NCT04180371 Recruiting I/II 288 MTD Nov 2019
G-202 CD13 NCT01056029

Completed

(NA)

I 30 MTD Dec 2012
PEN-221 CD13 NCT02936323

Completed

(Positive)

I/II 89 MTD Dec 2016
tTF–NGR CD13 NCT02902237

Completed

(Positive)

I 24 MTD Mar 2017
TH1902 SORT1 NCT04706962 Not recruiting I 70 MTD Mar 2021
CBP-1008 Frα and TRPV6 NCT04740398 Recruiting I 143 AEs Mar 2019
CBP-1018 PSMA and FRα NCT04928612 Recruiting I 170 AEs Nov 2021
SOR-C13 TRPV6 NCT01578564

Completed

(NA)

I 23 Plasma levels of SOR-C13 Jul 2015
Paclitaxel with Poliglumex PCSK9 NCT00487669

Completed

(Positive)

II 14 ORR Nov 2009
Paclitaxel with Poliglumex PCSK9 NCT00551733 Terminated III 450 OS Dec 2007
Paclitaxel with Poliglumex PCSK9 NCT00352690 Terminated II 10 OS Jun 2008
Paclitaxel with Poliglumex PCSK9 NCT00269828 Terminated III 600 OS Dec 2005
EP-100 GnRH NCT00949559

Completed

(NA)

I 38 Not provided Mar 2012
Lutathera NCT03325816

Completed

(Positive)

I/II 9 MTD Nov 2017
[18F]Fluciclatide αvβ5 and αvβ3 NCT02193672 Withdrawn I 0 Not provided Aug 2014
[18F]Fluciclatide αvβ5 and αvβ3 NCT01176500 Withdrawn I/II 0 Safety Nov 2011
[18F]RGD-K5 NCT00988936

Completed

(NA)

II 35 Usefulness Mar 2012
[18F]RGD-K5 NCT00743353

Completed

(NA)

I 16 Not provided Jan 2009

DLT dose-limiting toxicity, MTD maximum tolerated dose, AE adverse event, Cmax maximum plasma concentration, TEAE treatment-emergent adverse event, NA not available