Aldoxorubicin, the company’s main drug candidate, is a novel conjugate of doxorubicin, a commonly prescribed chemotherapeutic agent that binds to albumin, the most abundant protein in blood plasma, and is circulated throughout the body. Doxorubicin is used, either alone or in combination with other chemotherapy agents, as a treatment for a variety of cancers. The addition of aldoxorubicin is designed to essentially improve the release of doxorubicin in tumors, where it does the most good. This conjugate formulation has the potential to safely deliver greater amounts of doxorubicin directly to the tumor compared with standard doxorubicin treatment, which could lead to improved efficacy.
In a Phase 1 clinical trial, aldoxorubicin was administered in doses at up to six times the standard dosing of doxorubicin without an increase in observed side effects over those historically seen with doxorubicin. Additional tests have demonstrated statistically significant therapeutic results in breast, ovarian, pancreatic, and small cell lung cancers. Results of these studies were published in the peer-reviewed journal Investigational New Drugs. In tests for soft tissue sarcoma, median estimated progression-free survival for advanced soft tissue sarcoma patients in the trial was 6.4 months with a range of 1.0 to more than 10.7 months. This compares favorably with the historical median progression-free survival for this patient population of approximately 3 months.
CytRx holds the exclusive worldwide rights to aldoxorubicin.
For additional information, visit www.cytrx.com
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