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Table 2 A summary of growth factor-based therapeutic clinical trials in IVD

From: Therapeutic angiogenesis and tissue revascularization in ischemic vascular disease

First author

Phase year

Disease

Treatment

Subject(n) treatment/control

Findings

Ref

Stewart, Duncan J

Phase II 2008

CHD

Intramyocardial VEGF plasmid

48/45

No therapeutic effect

[37]

Richard J Powell

Phase II 2010

CLI

Intramuscular HGF plasmid

21/6

Improved ABI, no change in wound healing, major amputation, or death

[38]

Jill Belch

Phase III 2011

CLI

Intramuscular FGF plasmid

259/266

Failed to reduce amputation or death

[39]

Motoyuki Kumagai

Phase I/IIa 2016

CLI

Intramuscular FGF plasmid incorporated with gelatin hydrogel microspheres

10/0

Provided a safe and effective form of angiogenesis

[40]

Deev, R

Phase IIb/III 2018

CLI

Intramuscular VEGF165 plasmid

36/12

Improved ABI, TcPO2 and PWD

[41]

Gu, Y

Phase II 2019

CLI

Intramuscular HGF plasmid

150/50

Completed pain relief and improved the healing of ulcers

[42]

Barć, P

Phase II 2021

CLI

Intramuscular pIRES/VEGF165/HGF

14/14

Increased ABI and vascularization, decreased rest pain

[43]

  1. ABI Ankle brachial index, CHD Coronary heart disease, CLI Critical limb ischemia, FGF Fibroblast growth factor, HGF Hepatocyte growth factor, IVD Ischemic vascular disease, pIRES Plasmid internal ribosome entry site, PWD Pain-free walking distance, TcPO2 Transcutaneous oxygen pressure