ZIRCON Phase 3 IND Submitted to the US FDA

Melbourne (Australia) – 24 December 2019. Telix Pharmaceuticals Limited announces that it has submitted a Phase 3 IND application to the FDA for TLX250-CDx

Telix Pharmaceuticals Limited is pleased to announce that it has submitted a Phase 3 Investigational New Drug (IND) application to the United States Food and Drug Administration for TLX250-CDx (89Zr-girentuximab, for the imaging of renal cancer with Position Emission Tomography) as part of the international Phase 3 ZIRCON study.

The ZIRCON study is expected to commence enrolling US patients in Q1 2020.

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