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Pharmaceutical development of IPI-504, an Hsp90 inhibitor and clinical candidate for the treatment of cancer

Authors :
John Lee
Roger H. Pak
Louis Grenier
Vince Ammoscato
Michael Curtis
Kaiming Li
John Henderson
Matthew Campbell
Denise Mayes
Jason Kropp
Natalie Goltz
Bennett Carter
Johan Sebastian Basuki
Bradley Maurer
Gary Baker
James R. Wright
David Rusch
Rebecca Ahn
Brian C. Austad
Kris Depew
Joseph Helble
Jie Ge
Jason J. Piotrowski
Marlene R. Booth
Julian Adams
Mark Douglas
Steven G. Wong
Laila Kott
James R. Porter
Geoff E. Sylvester
Dumitru Ionescu
Jennifer R. Porter
Brendan Arsenault
Source :
Drug Development Research. 71:429-438
Publication Year :
2010
Publisher :
Wiley, 2010.

Abstract

IPI-504 (retaspimycin hydrochloride) is an Hsp90 inhibitor that is the subject of multiple clinical trials for the treatment of cancer. IPI-504 is an aqueous soluble (>200 mg/ml) hydroquinone hydrochloride salt of 17-(allylamino)-17-demethoxygeldanamycin (17-AAG), a quinone derivative also undergoing clinical evaluation, albeit with suboptimal formulations that address its inferior aqueous solubility (∼50 µg/ml). IPI-504 interconverts with 17-AAG in vivo through oxidation-reduction reactions that result in a dynamic redox equilibrium. The development challenges associated with redox active molecules are significant due to the pH, oxygen, and temperature sensitivities associated with such chemotypes. The API and sterile drug product manufacturing processes thus warrant the monitoring and control of these key variables. Furthermore, the pharmaceutical development challenges associated with cancer agents that are often fast-tracked due to unmet medical needs mandate a rapid development cycle with associated regulatory hurdles. Drug Dev Res 71: 429–438, 2010. © 2010 Wiley-Liss, Inc.

Details

ISSN :
02724391
Volume :
71
Database :
OpenAIRE
Journal :
Drug Development Research
Accession number :
edsair.doi...........1542e76e86b5ffd5bfe160834ae9e695
Full Text :
https://doi.org/10.1002/ddr.20383