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Active, not recruiting Phase 1 Interventional

ARX517/JNJ-95298177 as Monotherapy or Combination Therapy in Subjects With Metastatic Prostate Cancer

ClinicalTrials.gov ID: NCT04662580

Public ClinicalTrials.gov record NCT04662580. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 7:37 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1, Multicenter, Open-Label, Dose-Escalation, and Dose-Expansion Study to Evaluate the Safety, Pharmacokinetics, and Anti-Tumor Activity of ARX517 as Monotherapy and in Combination With Androgen Receptor Pathway Inhibitors in Subjects With Metastatic Prostate Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a phase 1 study to assess the safety and tolerability of ARX517 as monotherapy or combination therapy in adult subjects with metastatic prostate cancer (mPC).

Study identification

NCT ID
NCT04662580
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 1
Enrollment
183 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 3, 2021 (Actual)
Primary completion
Dec 31, 2026 (Estimated)
Completion
Dec 31, 2026 (Estimated)
Last update posted
Sep 28, 2026

2021 – 2026

United States locations

U.S. sites
12
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
UC San Diego Moores Cancer Center La Jolla California 92093 —
University of California, Los Angeles School of Medicine Los Angeles California 90095-3000 —
UCSF Medical Center at Mission Bay San Francisco California 94143-2350 —
Winship Cancer Institute of Emory University Atlanta Georgia 30322 —
Indiana University Melvin and Bren Simon Cancer Center Indianapolis Indiana 46202-5116 —
University of Michigan Comprehensive Cancer Center Ann Arbor Michigan 48109-5000 —
Washington University St. Louis School Medicine Siteman Cancer Center St Louis Missouri 63110 —
GU Research Network Omaha Nebraska 68130 —
Weill Cornell Medical College New York New York 10021-5663 —
University Hospitals Cleveland Medical Center Cleveland Ohio 44106 —
Carolina Urologic Research Center Myrtle Beach South Carolina 29572 —
University of Washington Seattle Washington 98101 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04662580, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 28, 2026 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04662580 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →