Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING Phase 1

Study Evaluating the Safety, Tolerability, and Efficacy of Xaluritamig in Combination With Androgen Receptor Pathway Inhibitors in Participants With Metastatic Hormone-sensitive Prostate Cancer

NCT07140900 · View on ClinicalTrials.gov ↗

Study Summary

The main objective of the trial is to evaluate the safety and tolerability of xaluritamig in combination with darolutamide or abiraterone.

Interventions

  • DRUG Darolutamide
  • DRUG Abiraterone
  • DRUG Xaluritamig

Study Locations (11)

Victoria

  • Cabrini Hospital — Clayton
  • Peter MacCallum Cancer Centre — Melbourne
  • The Alfred Hospital — Melbourne

Other

  • Kantonsspital Graubuenden — Chur
  • Centre Hospitalier Universitaire Vaudois — Lausanne
  • Kantonsspital Sankt Gallen — Sankt Gallen

New South Wales

  • Chris OBrien Lifehouse — Camperdown
  • Calvary Mater Newcastle Hospital — Waratah

Massachusetts

  • Dana Farber Cancer Institute — Boston

Minnesota

  • University of Minnesota — Minneapolis

Tennessee

  • Sarah Cannon Research Institute — Nashville

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2025-10-07
Est. Completion 2030-03-30
Phase Phase 1

Sponsor

Amgen

266 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07140900

The ClinicalTrials.gov registry entry for NCT07140900 describes a study currently listed as recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Amgen, which has 266 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Metastatic Hormone-sensitive Prostate Cancer (mHSPC) appearing as the primary indexed condition, and to 3 interventions — of which Darolutamide is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT07140900 reports 11 study locations spanning 6 distinct geographic areas — top geographies include Victoria, Other, New South Wales. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT07140900 about?

NCT07140900 is a clinical study titled "Study Evaluating the Safety, Tolerability, and Efficacy of Xaluritamig in Combination With Androgen Receptor Pathway Inhibitors in Participants With Metastatic Hormone-sensitive Prostate Cancer". The main objective of the trial is to evaluate the safety and tolerability of xaluritamig in combination with darolutamide or abiraterone.

What is the current status of trial NCT07140900?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 60 participants. The study started on 2025-10-07. Estimated completion is 2030-03-30.

What conditions does trial NCT07140900 study?

This clinical trial studies the following conditions: Metastatic Hormone-sensitive Prostate Cancer (mHSPC). These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07140900?

The interventions under investigation include: Darolutamide (DRUG), Abiraterone (DRUG), Xaluritamig (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07140900?

This trial is sponsored by Amgen, which has 266 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07140900 being conducted?

This trial has 11 study locations across Massachusetts, Minnesota, Tennessee, New South Wales, Victoria. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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