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

ACTIVE NOT RECRUITING Phase 3

Enzalutamide in First Line Androgen Deprivation Therapy for Metastatic Prostate Cancer

NCT02446405 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to determine the effectiveness of enzalutamide, versus a conventional non-steroidal anti androgen (NSAA), when combined with a luteinizing hormone releasing hormone analog (LHRHA) or surgical castration, as first line androgen deprivation therapy (ADT) for newly diagnosed metastatic prostate cancer.

Conditions Studied

Interventions

  • DRUG Enzalutamide
  • DRUG NSAA
  • DRUG LHRHA or Surgical Castration

Study Locations (20)

New South Wales

  • Chris O'Brien Lifehouse — Camperdown
  • Coffs Harbour Health Campus — Coffs Harbour
  • Concord Cancer Centre - Concord Repatriation General Hospital — Concord
  • St Vincent's Hospital Sydney — Darlinghurst
  • Nepean Cancer Care Centre — Kingswood
  • St. George Hospital — Kogarah
  • Central West Cancer Services — Orange
  • Port Macquarie Base Hospital — Port Macquarie
  • Prince of Wales Hospital — Randwick
  • Genesis Care North Shore — St Leonards
  • Tamworth Rural Referral Hospital — Tamworth
  • The Tweed Hospital — Tweed Heads
  • Riverina Cancer Care Centre — Wagga Wagga
  • Sydney Adventist Hospital — Wahroonga
  • Wollongong Hospital — Wollongong

Queensland

  • Sunshine Coast University Hospital — Birtinya
  • Townsville Hospital — Douglas
  • Royal Brisbane and Women's Hospital — Herston

Massachusetts

  • Dana Farber Cancer Institute — Boston

Northern Territory

  • Royal Darwin Hospital — Tiwi

Trial Details

FieldValue
Enrollment Target 1,125 participants
Start Date 2014-03
Est. Completion 2027-06-30
Phase Phase 3

Sponsor

University of Sydney

6 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02446405

The ClinicalTrials.gov registry entry for NCT02446405 describes a study currently listed as active not recruiting. It is categorized as Phase 3, 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 1,125 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Sydney, which has 6 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 Prostatic Neoplasms appearing as the primary indexed condition, and to 3 interventions — of which Enzalutamide 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: NCT02446405 reports 20 study locations spanning 4 distinct geographic areas — top geographies include New South Wales, Queensland, Massachusetts. 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 NCT02446405 about?

NCT02446405 is a clinical study titled "Enzalutamide in First Line Androgen Deprivation Therapy for Metastatic Prostate Cancer". The purpose of this study is to determine the effectiveness of enzalutamide, versus a conventional non-steroidal anti androgen (NSAA), when combined with a luteinizing hormone releasing hormone analog (LHRHA) or surgical castration, as first line androgen deprivation therapy (ADT) for newly diagnose...

What is the current status of trial NCT02446405?

This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 1,125 participants. The study started on 2014-03. Estimated completion is 2027-06-30.

What conditions does trial NCT02446405 study?

This clinical trial studies the following conditions: Prostatic Neoplasms. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02446405?

The interventions under investigation include: Enzalutamide (DRUG), NSAA (DRUG), LHRHA or Surgical Castration (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02446405?

This trial is sponsored by University of Sydney, which has 6 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02446405 being conducted?

This trial has 20 study locations across Massachusetts, New South Wales, Northern Territory, Queensland. 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