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NCT02903160 · ClinicalTrials.gov registry record · Phase 2

Prostate Cancer Intensive, Non-Cross Reactive Therapy (PRINT) for Castration Resistant Prostate Cancer (CRPC)

A Phase 2 study, sponsored by Icahn School of Medicine at Mount Sinai.

Completed
Registry status
Phase 2
Development phase
40
Enrollment target

NCT02903160 is a Phase 2 study that has completed, run by Icahn School of Medicine at Mount Sinai. The registered enrollment target is 40 participants.

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The verdict

NCT02903160, a Phase 2 study, has completed, sponsored by Icahn School of Medicine at Mount Sinai.

COMPLETED
Registry status
Phase 2
Development phase
40 participants
Enrollment target

Study Summary

The purpose of this study is to determine the clinical benefits of using a rapidly cycling, non-cross reactive regimen of FDA-approved prostate cancer therapeutic agents in the management of castration resistant prostate cancer. The hypothesis is that the identification of optimal combinations and sequencing of therapies can help prevent or delay the development of therapeutic drug resistance, and can be safely tolerated.

Interventions

  • DRUG Carboplatin
  • DRUG Prednisone
  • DRUG Abiraterone acetate
  • DRUG Radium-223 dichloride
  • DRUG cabazitaxel

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2017-01-13
Est. Completion 2021-11-15
Phase Phase 2

What the Registry Record Tells You About NCT02903160

The ClinicalTrials.gov registry entry for NCT02903160 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Icahn School of Medicine at Mount Sinai, which has 708 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 5 interventions - of which Carboplatin is the first listed.

NCT02903160 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02903160 about?

NCT02903160 is a clinical study titled "Prostate Cancer Intensive, Non-Cross Reactive Therapy (PRINT) for Castration Resistant Prostate Cancer (CRPC)". The purpose of this study is to determine the clinical benefits of using a rapidly cycling, non-cross reactive regimen of FDA-approved prostate cancer therapeutic agents in the management of castration resistant prostate cancer. The hypothesis is that the identification of optimal combinations and s...

What is the current status of trial NCT02903160?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 40 participants. The study started on 2017-01-13. Estimated completion is 2021-11-15.

What interventions are being tested in trial NCT02903160?

The interventions under investigation include: Carboplatin (DRUG), Prednisone (DRUG), Abiraterone acetate (DRUG), Radium-223 dichloride (DRUG), cabazitaxel (DRUG).

Who is sponsoring clinical trial NCT02903160?

This trial is sponsored by Icahn School of Medicine at Mount Sinai, which has 708 total clinical trials registered on ClinicalTrials.gov.

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.