ZIOPHARM Presents New Darinaparsin Preclinical Data at EORTC-NCI-AACR Meeting
-- Darinaparsin Demonstrates Potent Efficacy Effects in Various Solid Tumor Models --
The preclinical work was designed to study darinaparsin's cytotoxic and radiosensitizing effects against different solid tumor cell lines under both normoxic (NO) and hypoxic (HO) conditions. Hypoxia is an important condition in the microenvironment of solid tumor cells which creates resistance to cytotoxic drugs and radiation and causes cancer stem cells to re-grow the tumor. In these studies, hormone independent prostate cancer, pancreatic cancer, cervical cancer, and glioblastoma cell lines were treated with darinaparsin at concentrations ranging from 0.01 to 10 uM under either NO or HO conditions and irradiated with doses of 0 - 5 Gy. Results showed that darinaparsin is a potent cytotoxin under both NO and HO conditions and under HO when cells are resistant to radiation. Significant radiation enhancement was also observed in clonogenic assays under HO at clinically relevant doses, raising the potential for synergistic and dose-sparing radiation therapy. Darinaparsin's cytotoxic and radiation enhancing modes of action are distinct from other cytotoxic agents and were not dependent on generation of reactive oxygen species and DNA damage under HO.
"Darinaparsin's multiple mechanisms of action and potency provide for cytotoxicity and radiosensitization in a variety of tumor cell lines and environments," commented Dr. Knox. "This activity suggests a broad potential applicability for darinaparsin in the treatment of chemo- and radio-resistant solid tumors, with near term translational potential."
In September, ZIOPHARM announced that darinaparsin was granted Orphan
Drug Designation by the
About
Palifosfamide (ZymafosTM or ZIO-201) is a novel DNA cross-linker in class with bendamustine, ifosfamide, and cyclophosphamide. ZIOPHARM is currently enrolling patients in a randomized, double-blinded, placebo-controlled Phase III trial with palifosfamide administered intravenously for the treatment of metastatic soft tissue sarcoma in the front-line setting. The Company expects to initiate additional studies in the near-term, including a Phase I intravenous study of palifosfamide in combination with standard of care addressing small cell lung cancer and a Phase I study of oral palifosfamide.
Darinaparsin (ZinaparTM or ZIO-101) is a novel mitochondrial-targeted agent (organic arsenic) being developed intravenously for the treatment of peripheral T-cell lymphoma with a pivotal study expected to begin in late 2011. An oral form is in a Phase I trial in solid tumors.
Indibulin (ZybulinTM or ZIO-301) is a novel, oral tubulin binding agent that is expected to have several potential benefits including oral dosing, application in multi-drug resistant tumors, no neuropathy and minimal overall toxicity. It is currently being studied in Phase I/II in metastatic breast cancer.
ZIOPHARM's operations are located in
ZIOP-G
Forward-Looking Safe Harbor Statement:
This press release contains forward-looking statements for
tcook@ziopharm.com
or
Media:
david@argotpartners.com
Source:
News Provided by Acquire Media
