No OS efficacy readout is available. ClinicalTrials.gov shows NCT06520345 is recruiting with no results posted and estimated primary completion in Dec 2027. Public updates report only Part 1 safety/dosimetry and Part 2 initiation, not overall survival efficacy.
Registry lists the trial as Recruiting, with No Results Posted; primary completion is estimated Dec 2027 and the primary objective is rPFS comparison.
Telix says Part 2 randomized expansion has just begun and that preliminary Part 1 results would be disclosed after FDA engagement; no OS result reported.
Article describes Part 1 as meeting primary safety/dosimetry objectives and notes Part 2 randomized expansion will enroll about 490 patients; not an OS efficacy readout.