Bradmer announces Phase II results published in newly diagnosed glioblastoma which demonstrate improved survival and support upcoming Phase...(in a recently held guidance meeting. Bra...),Health

Date:2/26/2008

in a recently held guidance meeting. Bradmer has qualified the initial clinical sites in the study, received IRB approval or is in the process of completing the approval at the other sites and is continuing the IRB process and budgetary discussions at the first tier centers. The goal of the Phase III trial is to replicate the patient-specific dosing protocol as adjunct to standard of care in a controlled study at multiple leading GBM centers in North America.

Bradmer expects very shortly to submit the final manufacturing update and the standard clinical and regulatory documents to the FDA for their final review and approval. Allowing for the standard review period by the FDA, and pending its approval, the Company expects to be in a position to begin dosing GBM patients immediately after receiving notification from the FDA.

Bradmer's proposed Phase III trial, evaluating Neuradiab as a treatment for primary glioblastoma multiforme, is a randomized two arm multi-center study targeting 380 patients in each arm comparing the current standard of care with a group receiving Neuradiab as an adjunct to the current standard of care.

About Bradmer Pharmaceuticals Inc. (http://www.bradmerpharma.com)

Bradmer Pharmaceuticals is a biopharmaceutical company focused on the development and commercialization of new and innovative cancer therapies. Bradmer's lead clinical candidate, Neuradiab, was developed at Duke University Medical Center as a proprietary therapy for a particularly aggressive form of brain cancer, glioblastoma multiforme. To date, over US$60 million in grants and related support has driven research and development of the licensed treatment, which has been delivered to over 200 patients with promising results and has completed Phase II clinical trials at Duke University. Bradmer is currently in the process of organizing a pivotal multi-center clinical trial of the licensed treatment.
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SOURCE Bradmer Pharmaceuticals Inc. Copyright©2008 PR Newswire. All rights reserved

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