Posted on June 3, 2008 by crimsoncanary
Sunesis are cutting 60% of its workforce to concentrate on development of its lead compound voreloxin. Development of its CDK inhibitor SNS-032 currently in Phase I and and its Aurora kinase inhibitor SNS-314 will continue. Clinical data on these programs is expected later this year. Sunesis are seeking a development partner for SNS-314
Filed under: kinase | Tagged: aurora, CDK, licensing, phase I, SNS-032, SNS-314, SNS032, SNS314, Sunesis | Leave a Comment »
Posted on June 3, 2008 by crimsoncanary
Data presented at ASCO show ImmunoGen/Genentechs Trastuzumab-DM1 immunoconjugate demonstrates efficacy in metastatic breast cancer. The median progression-free survival in these patients was 9.8 months.
Filed under: Uncategorized | Tagged: Genentech, HER2, Herceptin, Immunogen, Pro-132365, Pro132365, Roche, Trastuzumab, Trastuzumab-DM1 | Leave a Comment »
Posted on June 3, 2008 by crimsoncanary
Nerviano have presented data on their kinase programs at ASCO:
PHA 848125 – CDK2, CDK1, CDK4 and TRKA – prolonged disease stabilization in 2 patients with advanced or metastatic solid tumours
PHA 739358 – Aurora – disease stabilization observed in 10/50 patients with advanced solid tumors. The drug was well tolerated
Filed under: kinase | Tagged: aurora, CDK1, CDK2, CDK4, kinase, nerviano, PHA-739358, PHA-848125, PHA739358, PHA848125, TRKA | Leave a Comment »
Posted on June 3, 2008 by crimsoncanary
Genmab have initiated a Phase I/II trial of zalutumumab (HuMax-EGFr) in colorectal cancer. The drug will be administered in combination with irinotecan
Filed under: Uncategorized | Tagged: EGF, Genmab, MAb, phase I, Phase II | Leave a Comment »
Posted on June 3, 2008 by crimsoncanary
Researchers at Jacobs University Bremen describe a new docking methodology using CDK2 inhibitors to demonstrate the method
Filed under: kinase | Tagged: kinase, Research, Univ Bremen | Leave a Comment »
Posted on June 3, 2008 by crimsoncanary
Phase II data to be presented at the lymphoma meeting in Lugano, Switzerland show Rigel’s Syk inhibitor R788 (fostamatinib disodium) to demonstrate efficacy in patients with relapsed or refractory B-cell non-Hodgkin’s lymphomas. R788 was well tolerated
Filed under: kinase | Tagged: fostamatinib, kinase, Pfizer, R788, rigel, syk | Leave a Comment »
Posted on June 3, 2008 by crimsoncanary
Phase II data presented at ASCO show Entremed’s drug MKC-1 to demonstrate efficacy in metastatic breast cancer. MKC-1 is a cell cycle inhibitor that targets mTor and PI3 kinases and HIF-1
Filed under: kinase | Tagged: Entremed, kinase, MKC-1, MKC1, mTOR, Phase II, PI3K | Leave a Comment »