Table 2.
Integrin inhibitors in clinical development as anticancer agents.
Antibodies | Other names | Target integrin | Comments on highest phase reached | Company | References |
---|---|---|---|---|---|
LM609 | Vitaxin, MEDI-552 | αVβ3 | Currently in Phase II | Scripps Research Institute | Brooks et al. 1994; Gutheil et al. 2000,McNeel et al. 2005 |
CNTO95 | αVβ3, αVβ5 | Currently in phase I | Centocor. Medarex | Trikha et al. 2004,Mullamitha et al. 2007 | |
Ha31/8 | α1β1 | Senger et al. 2002 | |||
17E6 | αVβ3 | Merck | Mitjans et al. 1995, 2000 | ||
Ha1/29 | α2β1 | Senger et al. 2002 | |||
NKI-SAM-1, JBS5 | α5β1 | Francis et al. 2002 | |||
M200 | Volociximab Eos-200-4 | α5β1 | Currently in phase II | Protein design Labs | Protein Design Labs, www.pdl.com |
Peptides | |||||
SCH 221153 | Kumar et al. 2001 | ||||
EMD 121974 | Cilengitide | αVβ5 | Currently in phase II | Merck KGaA, EMD Pharmaceuticals, National cancer Institute | Taga et al. 2002 |
ST1646 | αVβ3 | Belvisi et al. 2005 | |||
angiocidin | α2β1 | Sabherwal et al. 2006 | |||
18F-Galacto-RGD | Haubner et al. 2004, 2001 | ||||
Nonpeptidic | |||||
SJ749 | α5β1 | Marinelli et al. 2005; Maglott et al. 2006 | |||
E7820 | α2 subunit | Phase I | Eisai Medical Research | ||
S36578-2 | αVβ3, αVβ5 | Maubant et al. 2006 | |||
S-247 | αVβ3, αVβ5 | Reinmuth et al. 2003; Harms et al. 2004 |