
Oncology NEWS International
- Oncology NEWS International Vol 16 No 6
- Volume 16
- Issue 6
PEG-SN38 Shows Anti-Tumor Activity in Resistant Models
BRIDGEWATER, New Jersey—Enzon Pharmaceuticals, Inc.'s PEG-SN38, a novel polyethyleneglycol-SN38 conjugate, resulted in significant tumor growth inhibition in mice resistant to irinotecan (Camptosar) (a 25% decrease in tumor volume) and outperformed irinotecan when given as a second-round therapy to mice initially sensitive to irinotecan, the company said in a news release. The data were presented at the American Association for Cancer Research 2007 meeting (abstract 1494). Additionally, PEG-SN38 demonstrated long-lasting anti-tumor activity in mouse models of human breast and pancreatic cancers, the company said.
BRIDGEWATER, New JerseyEnzon Pharmaceuticals, Inc.'s PEG-SN38, a novel polyethyleneglycol-SN38 conjugate, resulted in significant tumor growth inhibition in mice resistant to irinotecan (Camptosar) (a 25% decrease in tumor volume) and outperformed irinotecan when given as a second-round therapy to mice initially sensitive to irinotecan, the company said in a news release. The data were presented at the American Association for Cancer Research 2007 meeting (abstract 1494). Additionally, PEG-SN38 demonstrated long-lasting anti-tumor activity in mouse models of human breast and pancreatic cancers, the company said.
Articles in this issue
about 19 years ago
ACS Launches Major Epidemiology Studyabout 19 years ago
Pt Selection Key to Radioembolization of Liver Ca'sabout 19 years ago
Million Dollar Gotham Prize Announcedabout 19 years ago
Diagnostic Dilemma: GI Diseaseabout 19 years ago
Velcade/Doxil Approved for Relapsed or Refractory Multiple Myeloma Ptsabout 19 years ago
Junovan Fails to Win ODAC Nod for Osteosarcoma Treatmentabout 19 years ago
Surveillance Colonoscopy Guidelines Not Being Followedabout 19 years ago
Removing Stage IV Primary May Cut Mortalityabout 19 years ago
Nuclear Export Inhibitors Testing Moving Forwardabout 19 years ago
ODAC: orBec Yields No 'Substantial Efficacy' in GI GVHD















































































