Top page > What's new

What's new

2010.06.17
CanBas and Takeda to Terminate Collaboration for CBP501 for the Treatment of Cancer
2009.07.07
Phase 2 for the clinical study of CBP501, an anticancer drug for non-small-cell lung carcinoma, has begun PDF (60.1KB)
2009.04.03
To increase the efficiency of drug screening methods, NEC's "ChemMiner(TM)" technology was introduced to the screen compounds in candidate pharmaceuticals
2009.10.16
Phase 2 for the clinical study of CBP501, an anticancer drug for malignant pleural mesothelioma, has begun PDF (51KB)
2008.06.01
Report of the Phase 1 clinical study of CBP501 at ASCO2008
2008.05.01
Phase 2 clinical study of the combined usage of CBP501, Pemetrexed and Cisplatin in patients with Malignant Pleural Mesothelioma initiated in the US
2007.04.02
CanBas delivered the anticancer drug CBP501 to Takeda Pharmaceuticals. In the US, joint development and co-op promotion were started
2007.03.30
CanBas and Takeda Pharmaceuticals to Sign a Joint Venture Agreement for Investigational Compounds for Treatment of Cancer
2007.01.01
Paper on CBP501 published in Molecular Cancer Therapeutics
2006.11.01
Midterm results of the CBP501 Phase 1 clinical study reported in the 18th EORTC-NCI-AACR
2006.10.01
Phase 1 clinical study for CBP501 / Cisplatin combination therapy has been initiated in the US
2006.02.22
Patent for the most advanced compound CBP501 issued by USPTO PDF (34.7KB)
2006.02.16
2nd closing of 4th financing round, total procurement fund to JPY 2,500 million PDF (36.4KB)
2005.12.29
CanBas to procure JPY 2,360 million to invest in clinical studies of anticancer drugs
2005.11.01
4th financing round results in the appropriation of JPY 2,359 million for clinical study costs PDF (37.1KB)
2005.07.01
Journal of the National Cancer Institute Vol. 97, No. 14, 1026-1028, July 20, 2005 "New Checkpoint Blockers Begin Human Trials"
2005.05.01
Phase 1 clinical study for CBP501 has been initiated in the US

▲Return to top

Company information

  • What's new