Brain tumor drug receives rare disease designations from the FDA

Brain tumor drug receives rare disease designations from the FDA
The Food and Drug Administration has given Orphan Disease Designation and Rare Pediatric Disease Designation to OKN-007, an experimental brain cancer treatment currently in Phase 2 clinical trials at eight U.S. sites. The drug was discovered by Oklahoma Medical Research Foundation scientists Rheal Towner, Ph.D., (front) and Robert Floyd, Ph.D. (back). Credit: Oklahoma Medical Research Foundation

The U.S. Food and Drug Administration has awarded Rare Pediatric Disease Designation (RPDD) for diffuse intrinsic pontine glioma (DIPG) and Orphan Drug Designation for treatment of malignant glioma to OKN-007, an investigational drug discovered at the Oklahoma Medical Research Foundation and being developed by Oblato, Inc.

DIPG is a fast-growing that starts in the . It is one of several sub-categories of malignant gliomas, deadly cancers of the brain and .

"We are very pleased to receive the successful designations from the FDA for our proprietary compound OKN-007," said Oblato President and Chief Executive Officer Won S. Yang. These designation programs provide for special status and priority review of regulatory applications for new therapies for rare pediatric or "orphan" diseases, conditions that affect limited patient populations.

According to the National Brain Tumor Society, approximately 26,000 Americans will be diagnosed with primary malignant brain tumors this year. Of those, reports that up to 300 will be cases of DIPG.

OKN-007 was initially discovered by OMRF scientists Rheal Towner, Ph.D., and Robert Floyd, Ph.D. Oblato acquired all rights to OKN-007 from OMRF, and the company is currently testing the investigational drug in a Phase 2 clinical study of 56 patients suffering from recurrent glioblastoma, the most aggressive form of glioma. The patients are being treated with the drug in combination with another medication, temozolomide, at eight sites in the U.S.

In pre- at OMRF, Towner has also shown that OKN-007 inhibits growth of human DIPG tumors implanted in experimental models. Oblato is planning to begin clinical trials in DIPG patients in 2021. "Right now, there is no for this deadly brain cancer," said Towner.

Going forward, Oblato and OMRF will continue collaborating, with a focus on improving treatment for patients suffering from a variety of solid-tumor cancers.

"OMRF and Oblato are committed to a single goal: helping patients overcome these life-threatening illnesses," said OMRF Director of Technology Ventures Andrew Westmuckett, Ph.D. "Our hope is that OKN-007 can transform the therapeutic landscape."

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Provided by Oklahoma Medical Research Foundation
Citation: Brain tumor drug receives rare disease designations from the FDA (2020, September 2) retrieved 30 June 2022 from
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