[PDF][PDF] Pharmaceutical development of a parenteral lyophilised dosage form for the novel anticancer agent C1311

MWJ Den Brok, B Nuijen… - … of selected novel …, 2005 - researchgate.net
Abstract C1311 (5-[[2-(diethylamino) ethyl] amino]-8-hydroxyimidazo [4, 5, 1-de]-acridin-6-
onedihydrochloride trihydrate) is the lead compound from the group of imidazoacridinones …

Pharmacokinetics and tissue distribution of the imidazoacridinone C1311 in tumour-bearing mice

CR Calabrese, MC Bibby, JA Double… - Cancer chemotherapy …, 1998 - Springer
C1311 is the most active member of a new series of rationally designed anti-cancer agents,
the imidazoacridinones, which has shown promising pre-clinical anti-tumour activity in vitro …

Development and validation of an LC–UV method for the quantification and purity determination of the novel anticancer agent C1311 and its pharmaceutical dosage …

MWJ den Brok, B Nuijen, MJX Hillebrand… - … of pharmaceutical and …, 2005 - Elsevier
C1311 (5-[[2-(diethylamino) ethyl] amino]-8-hydroxyimidazo [4, 5, 1-de]-acridin-6-one-
dihydrochloride trihydrate) is the lead compound from the group of imidazoacridinones, a …

Analysis of the imidazoacridinone C1311 by high-performance liquid chromatography

CR Calabrese, PM Loadman - Journal of Chromatography B: Biomedical …, 1997 - Elsevier
The imidazoacridinone C1311 has shown anti-tumour activity both in vitro and in vivo,
prompting its acceptance for Phase I clinical trials. A high-performance liquid …

Preclinical evaluation of novel imidazoacridinone derivatives with potent activity against experimental colorectal cancer

AM Burger, JA Double, J Konopa, MC Bibby - British journal of cancer, 1996 - nature.com
Novel imidazoacridinone derivatives, C1310 and C1311, have been evaluated for their
potential to inhibit tumour cell growth in vitro and in vivo. A cell line panel, including seven …

Compatibility and stability of the novel anti-cancer agent C1311 in infusion devices and its in vitro biocompatibility

MWJ den Brok, B Nuijen, R Harms… - Journal of Oncology …, 2005 - journals.sagepub.com
C1311 is the lead compound from the imidazoacridinones, a novel group of rationally
designed anti-cancer agents. The compound is pharmaceutically formulated as a lyophilized …

[PDF][PDF] Pharmaceutical development of a parenteral lyophilised formulation of the investigational anticancer agent ES-285. HCl.

MW Den Brok, B Nuijen, DM Meijer… - … of selected novel …, 2005 - researchgate.net
Abstract ES-285. HCl [(2S, 3R)-2-aminooctadecan-3-ol hydrochloride] is a novel
investigational anticancer agent which has shown activity against various tumour cell lines …

In vivo metabolism of the antitumor imidazoacridinone C1311 in the mouse and in vitro comparison with humans

CR Calabrese, PM Loadman, LSE Lim, MC Bibby… - Drug metabolism and …, 1999 - ASPET
C1311 has emerged as the lead compound from a novel group of anticancer agents, the
imidazoacridinones, and will be entering clinical trials shortly. Previous murine …

Comparative Cytotoxicity of C-1311 in Colon Cancer In Vitro and In Vivo Using the Hollow Fiber Assay

N Alami, J Paterson, S Belanger, S Juste… - Journal of …, 2007 - Taylor & Francis
The aim of this study was to investigate the antiproliferative effects of C-1311 (Symadex), a
member of the imidazoacridinone family, in human colorectal cancer cells. In the in vitro …

Evaluation of the safety of C-1311 (SYMADEX) administered in a phase 1 dose escalation trial as a weekly infusion for 3 consecutive weeks in patients with advanced …

N Isambert, M Campone, E Bourbouloux… - European Journal of …, 2010 - Elsevier
PURPOSE: C-1311 is a member of the novel imidazoacridinone family of anticancer agents.
This phase 1 trial was designed to investigate the safety, tolerability and preliminary anti …