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NCT07476001 · ClinicalTrials.gov registry record · Phase 2

Phase 2a Study of High-Dose Testosterone Followed by Radioligand Therapy in mCRPC

A Phase 2 study of Metastatic Castration-Resistant Prostate Cancer, sponsored by H. Lee Moffitt Cancer Center and Research Institute.

Recruiting
Registry status
Phase 2
Development phase
12
Enrollment target
1
Study location

NCT07476001 is a Phase 2 study of Metastatic Castration-Resistant Prostate Cancer that is actively recruiting participants, run by H. Lee Moffitt Cancer Center and Research Institute. The registered enrollment target is 12 participants, below the 198-participant average among 69 other Metastatic Castration-Resistant Prostate Cancer trials with a reported enrollment target (94% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT07476001, a Phase 2 study of Metastatic Castration-Resistant Prostate Cancer, is actively recruiting participants, sponsored by H. Lee Moffitt Cancer Center and Research Institute.

RECRUITING
Registry status
Phase 2
Development phase
12 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to evaluate whether high-dose testosterone followed by targeted radioligand therapy (TRT) is effective in treating metastatic castration resistant prostate cancer. Participants will be asked to spend about 6 months in this study. Participants will take study drug for 3.5 months.

Interventions

  • DRUG Testosterone cypionate (Tc)
  • DRUG ADT with Luteinizing hormone-releasing hormone (LHRH) analog
  • DRUG PSMA-617

Study Locations (1)

Florida

  • Moffitt Cancer Center - Tampa

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2026-03
Est. Completion 2027-09
Phase Phase 2

What the Registry Record Tells You About NCT07476001

The ClinicalTrials.gov registry entry for NCT07476001 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 12 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 198-participant average among 69 other Metastatic Castration-Resistant Prostate Cancer trials with a reported enrollment target (94% lower). The listed sponsor is H. Lee Moffitt Cancer Center and Research Institute, which has 502 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Metastatic Castration-Resistant Prostate Cancer appearing as the primary indexed condition, and to 3 interventions - of which Testosterone cypionate (Tc) is the first listed.

NCT07476001 reports 1 study location spanning 1 distinct geographic area - top geographies include Florida.

Frequently Asked Questions

What is clinical trial NCT07476001 about?

NCT07476001 is a clinical study titled "Phase 2a Study of High-Dose Testosterone Followed by Radioligand Therapy in mCRPC". The purpose of this study is to evaluate whether high-dose testosterone followed by targeted radioligand therapy (TRT) is effective in treating metastatic castration resistant prostate cancer. Participants will be asked to spend about 6 months in this study. Participants will take study drug for 3.5...

What is the current status of trial NCT07476001?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 12 participants. The study started on 2026-03. Estimated completion is 2027-09.

What conditions does trial NCT07476001 study?

This clinical trial studies the following conditions: Metastatic Castration-Resistant Prostate Cancer.

What interventions are being tested in trial NCT07476001?

The interventions under investigation include: Testosterone cypionate (Tc) (DRUG), ADT with Luteinizing hormone-releasing hormone (LHRH) analog (DRUG), PSMA-617 (DRUG).

Who is sponsoring clinical trial NCT07476001?

This trial is sponsored by H. Lee Moffitt Cancer Center and Research Institute, which has 502 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07476001 being conducted?

This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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