Novel therapeutics categorized by pharmacologic class and target of interaction.
Mechanism Modulated (Pharmacologic Class) . | Agent . |
---|---|
Survival Signals | |
Antiangiogenic | thalidomide (Thalomid™) CC5013 (Revimid™), CC1088 bevacizumab (Avastin™) arsenic trioxide (Trisenox™) |
Receptor tyrosine kinase inhibitors | SU5416, SU11248 PTK787 AG13736 imatinib mesylate (Gleevec™) |
Protein kinase C inhibitor | PKC412 |
Matrix metalloprotease inhibitor | AG3340 (Prinomastat™) |
Farnesyl transferase Inhibitors | R115777 (Zarnestra™) SCH66336 (lonafarnib; Sarasar™) |
Genetic Integrity | |
Immunoconjugate | gemtuzumab ozogamicin (Mylotarg™) |
P-glycoprotein antagonist | cyclosporine-A quinine sulfate LY335979 (zosuquidar trihydrochloride) |
Mechanism Modulated (Pharmacologic Class) . | Agent . |
---|---|
Survival Signals | |
Antiangiogenic | thalidomide (Thalomid™) CC5013 (Revimid™), CC1088 bevacizumab (Avastin™) arsenic trioxide (Trisenox™) |
Receptor tyrosine kinase inhibitors | SU5416, SU11248 PTK787 AG13736 imatinib mesylate (Gleevec™) |
Protein kinase C inhibitor | PKC412 |
Matrix metalloprotease inhibitor | AG3340 (Prinomastat™) |
Farnesyl transferase Inhibitors | R115777 (Zarnestra™) SCH66336 (lonafarnib; Sarasar™) |
Genetic Integrity | |
Immunoconjugate | gemtuzumab ozogamicin (Mylotarg™) |
P-glycoprotein antagonist | cyclosporine-A quinine sulfate LY335979 (zosuquidar trihydrochloride) |