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Table 8 Clinical trials of PDC drugs for lung cancer treatment

From: Drug conjugates for the treatment of lung cancer: from drug discovery to clinical practice

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Withdrawn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Withdrawn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Withdrawn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

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