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DelMar Pharmaceuticals To Present At The 15th Annual Rodman & Renshaw Global Investment Conference
Date:9/3/2013

a potential new treatment for GBM patients who have failed standard therapies. In June, DelMar reported encouraging interim results from the trial at the American Society for Clinical Oncology (ASCO). Last month, the FDA allowed DelMar to accelerate the dose-escalation in the clinical trial.

Temodar generates more than US$950 million annually in global revenues, primarily from the treatment of brain cancer.

In addition to its clinical activities in the United States, DelMar has acquired the commercial rights to VAL-083 in China, where it is approved for chronic myelogenous leukemia (CML) and lung cancer. DelMar and its manufacturing partner, Guangxi Wuzhou Pharmaceuticals, plan to work with leading clinicians in China to develop new post-market data to support the sales and marketing of VAL-083 in these indications in China and to expand the market opportunities for the drug on a worldwide basis.

DelMar's Recent Highlights:

  • August: FDA Allows Accelerated Dose-escalation for VAL-083 Clinical Trial in Gliobastoma
  • July: VAL-083 Clinical Trial in Glioblastoma Expands to UC San Francisco (UCSF)
  • July: DelMar and Guangxi Wuzhou Announce Chinese Government Funding Award
  • July: First U.S. Patent Issued for VAL-083, Part of International IP Strategy

Follow us on Twitter @DelMarPharma and use #Rodman2013 for conference updates.  

About DelMar Pharmaceuticals

DelMar Pharmaceuticals was founded in 2010 to develop and commercialize proven cancer therapies in new orphan drug indications where patients are failing modern targeted or biologic treatments. The Company's lead asset, VAL-083, is currently undergoing clinical trials in the U.S. as a potential treatment for refractory glioblastoma multiforme, the most
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