Curis Developing Multi-Target Inhibitor Drug Compounds
Posted on: Friday, 28 September 2007, 06:00 CDT
Cancer drug-development company Curis has said that it is developing a number of small molecule multi-target inhibitor drug compounds.
Providing an update on CUDC-101 and other preclinical drug candidates under its targeted cancer drug development platform, the company said CUDC-101 is its lead multi-target inhibitor drug candidate under development, which is designed to inhibit epidermal growth factor receptor and Her2, two validated cancer targets, as well as histone deacetylase (HDAC).
Curis has generated in vitro and in vivo preclinical data to support ongoing CUDC-101 preclinical development efforts. CUDC-101 displays anti-proliferation and apoptosis, or programmed cell death, inducing activities in vitro against a broad range of cancer cell types including lung, breast, prostate, colon, liver and pancreas.
CUDC-101 also inhibits the in vivo growth of various human cancers in eleven standard mouse tumor xenograft models in which human cancer cells are transplanted into the mouse, allowing the cancer cells to grow into established tumors.
Daniel Passeri, president and CEO of Curis, said: "We believe that HDAC inhibition is a very promising non-kinase target for cancer therapy. Currently there is one FDA-approved HDAC inhibitor and several other HDAC drug candidates in clinical trials for cancer."
Source: Datamonitor
Related Articles
- New Cancer Drug Delivery System Is Effective and Reversible
- Curis Initiates Dosing in Phase I Study of Cancer Drug
- Curis Selects New Development Candidate From Cancer Drug Platform
- NexGenix Pharmaceuticals Presents Data on a Novel Small Molecule Inhibitor of Heat Shock Protein 90 (Hsp90) at the GTCbio Cancer Drugs Research & Development Conference
- Renal Cancer Drug Pipeline Update Lists All Drugs and Gives You a Progress Analysis on Each One of Them
- Curis Selects First Development Candidate From Its Targeted Cancer Drug Development Platform
- Geron Presents Early Clinical Trial Data for Its Telomerase Inhibitor Cancer Drug
- Serono Cancer Drug Fails to Meet Trial Targets
- Geron Announces Publication Characterizing GRN163L, Its Telomerase Inhibitor Drug Currently in Clinical Development for Cancer
- Second Gene Mutation Explains Lung Cancer Drug Resistance
User Comments (0)

RSS Feeds