FDA Grants Telix ODD for Glioma PET Imaging Agent

By News Release

Low Grade Glioma | The Neurosurgical Atlas, by Aaron Cohen-Gadol, M.D.Telix Pharmaceuticals Limited has announced that the United States Food and Drug Administration (FDA) has granted Orphan Drug Designation (ODD) for O-(2-[18F]fluoroethyl)-L-tyrosine (18F-FET), for the positron emission tomography (PET) imaging of glioma, a type of brain tumor.

The granting of an ODD for 18F-FET qualifies Telix for various drug development incentives which may include FDA-administered market exclusivity for seven years, waived FDA prescription drug user fees, and tax credits for R&D and clinical development costs.

Telix CEO Dr Christian Behrenbruch said, “PET imaging of the brain is increasingly used to supplement conventional imaging with MRI, which for many years has been the primary clinical imaging modality in patients with glioma at all stages of disease. The granting of an Orphan Drug Designation by the FDA for 18F-FET provides Telix with the option to develop this valuable PET imaging agent commercially, to ensure it is available to patients with glioma across the disease spectrum. 18F-FET’s relevance as a patient selection and therapeutic monitoring tool for TLX101 is particularly beneficial to the company.”

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FDA Grants Telix ODD for Glioma PET Imaging Agent.  Appl Radiol. 

By News Release| October 07, 2020

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