Telix Pharmaceuticals Limited provided an update on the progress of the ZIRCON Phase 3 study for the imaging of renal cancer with Positron Emission Tomography (PET). ZIRCON is a 252 patient Phase 3 pivotal study, currently being conducted at 34 sites globally. The study has exceeded 50% recruitment despite significantly reduced recruitment over the last 12 months due to a pandemic operating environment. With at least 80% of sites in the study back recruiting into clinical trials, recruitment has significantly accelerated and indicative patient recruitment is 5-10 patients per week. TLX250-CDx drug product for the ZIRCON trial is provided from Telix's manufacturing and dispensing sites in Canada, United States, Turkey and the Netherlands. Transportation and logistics have also largely enabled a resumption to normal drug product delivery schedules, including to Australia. The company expects the trial to complete recruitment in the next 4-5 months, subject to ongoing pandemic conditions. Telix expects to commence the FDA Biologics License Application (BLA) consultation process before end-calendar year, as planned. A Japanese bridging study to ZIRCON has also been successfully completed.