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RECRUITING Phase 3

Accelerated v's Standard BEP Chemotherapy for Patients With Intermediate and Poor-risk Metastatic Germ Cell Tumours

NCT02582697 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to determine whether accelerated BEP chemotherapy is more effective than standard BEP chemotherapy in males with intermediate and poor-risk metastatic germ cell tumours.

Conditions Studied

Interventions

  • DRUG Cisplatin
  • DRUG Etoposide
  • DRUG Filgrastim
  • DRUG Bleomycin (active name: Bleomycin Sulfate)
  • DRUG Pegylated G-CSF (Pegfilgrastim)

Study Locations (20)

New South Wales

  • Calvary Mater Newcastle — Newcastle
  • Royal North Shore Hospital — St Leonards
  • Prince of Wales Hospital — Sydney
  • Chris O'Brien Lifehouse — Sydney
  • Macquarie Cancer Clinical Trials — Sydney
  • Concord Repatriation General Hospital — Sydney
  • Westmead Hospital — Sydney
  • Nepean Hospital — Sydney
  • Tweed Hospital — Tweed Heads
  • SAN Clinical Trials Unit — Wahroonga

Queensland

  • Royal Brisbane & Women's Hospital — Brisbane
  • Queensland Children's Hospital — South Brisbane
  • Princess Alexandra — Woolloongabba

Victoria

  • Box Hill Hospital — Box Hill
  • Peter MacCallum Cancer Centre — East Melbourne
  • Austin Health — Heidelberg

South Australia

  • Royal Adelaide Hospital — Adelaide
  • Flinders Medical Centre — Bedford Park

New York

  • Memorial Sloan Kettering Cancer Centre — New York

Tasmania

  • Royal Hobart Hospital — Hobart

Trial Details

FieldValue
Enrollment Target 500 participants
Start Date 2014-02
Est. Completion 2029-12-31
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 NCT02582697

The ClinicalTrials.gov registry entry for NCT02582697 describes a study currently listed as 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 500 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 Germ Cell Tumor appearing as the primary indexed condition, and to 5 interventions — of which Cisplatin 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: NCT02582697 reports 20 study locations spanning 6 distinct geographic areas — top geographies include New South Wales, Queensland, Victoria. 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 NCT02582697 about?

NCT02582697 is a clinical study titled "Accelerated v's Standard BEP Chemotherapy for Patients With Intermediate and Poor-risk Metastatic Germ Cell Tumours". The purpose of this study is to determine whether accelerated BEP chemotherapy is more effective than standard BEP chemotherapy in males with intermediate and poor-risk metastatic germ cell tumours.

What is the current status of trial NCT02582697?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 500 participants. The study started on 2014-02. Estimated completion is 2029-12-31.

What conditions does trial NCT02582697 study?

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

What interventions are being tested in trial NCT02582697?

The interventions under investigation include: Cisplatin (DRUG), Etoposide (DRUG), Filgrastim (DRUG), Bleomycin (active name: Bleomycin Sulfate) (DRUG), Pegylated G-CSF (Pegfilgrastim) (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02582697?

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 NCT02582697 being conducted?

This trial has 20 study locations across New York, New South Wales, Queensland, South Australia, Tasmania. 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