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COMPLETED

Real-World Study of Enzalutamide and Abiraterone Acetate (With Prednisone) Tolerability

NCT02663193 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to characterize the tolerability profiles of enzalutamide and abiraterone acetate (with prednisone) -with specific focus on central nervous system (CNS) tolerability-and quality of life (QoL) after approximately 2 months of participants starting treatment with one of these agents for metastatic castration-resistant prostate cancer (mCRPC).

Conditions Studied

Interventions

  • OTHER No Intervention

Study Locations (20)

New Jersey

  • — Englewood
  • — Lawrenceville
  • — Morristown

Indiana

  • — Indianapolis
  • — Jeffersonville

New York

  • — Poughkeepsie
  • — Syracuse

Pennsylvania

  • — Bala-Cynwyd
  • — Lancaster

South Carolina

  • — Charleston
  • — Myrtle Beach

Alabama

  • — Homewood

California

  • — La Mesa

Colorado

  • — Wheat Ridge

Trial Details

FieldValue
Enrollment Target 108 participants
Start Date 2015-12
Est. Completion 2017-01

Sponsor

Janssen Scientific Affairs

10 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02663193

The ClinicalTrials.gov registry entry for NCT02663193 describes a study currently listed as completed. It is categorized as an unspecified phase, 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 108 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Janssen Scientific Affairs, which has 10 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 Prostate Cancer appearing as the primary indexed condition, and to 1 intervention — of which No Intervention 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: NCT02663193 reports 20 study locations spanning 14 distinct geographic areas — top geographies include New Jersey, Indiana, New York. 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 NCT02663193 about?

NCT02663193 is a clinical study titled "Real-World Study of Enzalutamide and Abiraterone Acetate (With Prednisone) Tolerability". The purpose of this study is to characterize the tolerability profiles of enzalutamide and abiraterone acetate (with prednisone) -with specific focus on central nervous system (CNS) tolerability-and quality of life (QoL) after approximately 2 months of participants starting treatment with one of the...

What is the current status of trial NCT02663193?

This trial is currently completed. The enrollment target is 108 participants. The study started on 2015-12. Estimated completion is 2017-01.

What conditions does trial NCT02663193 study?

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

What interventions are being tested in trial NCT02663193?

The interventions under investigation include: No Intervention (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02663193?

This trial is sponsored by Janssen Scientific Affairs, which has 10 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02663193 being conducted?

This trial has 20 study locations across Alabama, California, Colorado, Florida, Indiana. 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