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Clinical trialNCT06549465RecruitingPhase 2Interventional

Study Evaluating Dosimetry, Randomized Dose Optimization, Dose Escalation and Efficacy of Ac-225 Rosopatamab Tetraxetan in Participants With PSMA PET-Positive Castration-Resistant Prostate Cancer (CRPC)

SponsorConvergent TherapeuticsEnrollment93PSMA PET-Positive Castration-Resistant Prostate Cancer
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

This is a four-part study evaluating the safety and efficacy of a PSMA-directed radioantibody (rosopatamab tetraxetan, conjugated to either In-111 or Ac-225). Part 1 will consist of one administration of In-111-rosopatamab tetraxetan to characterize the biodistribution of the radioantibody to target organs and prostate cancer lesions. Participants then will be enrolled into either Part 2 (Dose Optimization) or Part 3 (Dose Escalation and Expansion) depending on their prior treatment history. Part 4 will be an extended regimen in dose escalation and expansion. Participants qualifying for Part 2 will be randomized to receive Ac-225 rosopatamab tetraxetan in a single fractionated cycle (dose administration on Day 1 and Day 15) at either 45 or 60 kBq/Kg. Participants qualifying for Part 3 must have received prior Lu-177-PSMA-radioligand therapy and will receive Ac-225 rosopatamab tetraxetan in a single fractionated cycle at 45, 55, or 60 kBq/Kg. Dose limiting toxicities (DLTs) will be monitored in Part 3 to determine the recommended phase 2 dose (RP2D), and the study may enroll additional participants to be treated with the RP2D dose level. Participants qualifying for Part 4 will initially receive two doses (dose administration on Day 1 and Day 15) at the dose level selected in Part 2, followed by a single third dose of Ac-225 rosopatamab tetraxetan administered approximately 12 weeks after completion of the Part 2 fractionated dosing regimen. The starting dose level for Part 4 will be 22 kBq/kg (or fixed activity equivalent). Dose limiting toxicities (DLTs) will be monitored following administration of the third dose in Part 4 to determine the recommended phase 2 dose (RP2D) of a third dose of Ac-225 rosopatamab tetraxetan. Participants enrolled into any part will attend study visits which will include blood samples, electrocardiogram (ECG), radiographic imaging, and physical examinations along with other assessments.

Investigators

No overall officials are registered on this study record. Site-level investigators, where published, appear with their sites below. Why? →

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

9 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • University of California San Diego

    San Diego, California, United States

    Rana McKay, MD
    Recruiting
  • Dana-Farber Cancer Institute

    Boston, Massachusetts, United States

    Praful Ravi, MB, BChir, MRCP
    Recruiting
  • Washington University in St. Louis

    St Louis, Missouri, United States

    Vikas Prasad, MD, PhD
    Recruiting
  • X Cancer Omaha / Urology Cancer Center

    Omaha, Nebraska, United States

    Luke Nordquist, MD
    Recruiting
  • Laura & Isaac Perlmutter Cancer Center

    New York, New York, United States

    David Wise, MD
    Recruiting
  • Memorial Sloan Kettering Cancer Center

    New York, New York, United States

    Anis Hamid, MD
    Recruiting
  • New York Presbyterian/weill Cornell Medical Center

    New York, New York, United States

    Cora Sternberg, MD
    Recruiting
  • Duke University Medical Center

    Durham, North Carolina, United States

    Daniel George, MD
    Recruiting
  • the Cleveland Clinic Foundation

    Cleveland, Ohio, United States

    Shilpa Gupta, MD
    Recruiting

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

45 kBq55 kBq60 kBqIn-111 rosopatamab tetraxetan45 kBq/kg or equivalent fixed dose activity Ac-225 rosopatamab tetraxetan55 kBq/kg or equivalent fixed dose activity Ac-225 rosopatamab tetraxetan60 kBq/kg or equivalent fixed dose activity Ac-225 rosopatamab tetraxetanSingle dose 22 kBq/kg or equivalent fixed dose activity Ac-225 rosopatamab tetraxetanSingle dose 34 kBq/kg or equivalent fixed dose activity Ac-225 rosopatamab tetraxetanSingle dose 45 kBq/kg or equivalent fixed dose activity Ac-225 rosopatamab tetraxetan
Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
6 Aug 2024
Primary completion
20 Apr 2027
Completion
20 Apr 2027
Last update posted
20 Jul 2026
Registered enrollment
93
Registry id
NCT06549465

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.