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Lead-212 PSV359 Therapy for Patients With Solid Tumors

← catalyst calendar

NCT06710756 · readout in 530 d

Sponsored by Perspective Therapeutics (industry) · CATX — their whole pipeline →.

Phase
Phase 1/2
Status
Recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
112estimated
Sites
11
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2025-04-28actualWhen the study began enrolling
Primary completion2028-01-31estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2032-05-28estimatedThe whole study's end, after follow-up
First posted2024-11-29actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-06actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Pancreatic Ductal Adenocarcinoma
  • Gastric Cancer
  • Esophageal Cancer
  • Colorectal Cancer
  • Ovarian Cancer
  • Head and Neck Cancer
  • Sarcoma
  • Mesothelioma

Interventions

  • Drug: [203Pb]Pb-PSV359
  • Drug: [212Pb]Pb-PSV359

Primary outcomes

what the primary-completion date above is the date OF
Determination of safety and tolerability of [203Pb]Pb-PSV359
measured 30 days (±1day) post dose
Determination of safety and tolerability of [212Pb]Pb-PSV359
measured Up to 3 years
To determine the recommended phase 2 dose of [212Pb]Pb-PSV359
measured Up to approximately 6 months

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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