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NCT03442556 · ClinicalTrials.gov registry record · Phase 2

Docetaxel, Carboplatin, and Rucaparib Camsylate in Treating Patients With Metastatic Castration Resistant Prostate Cancer With Homologous Recombination DNA Repair Deficiency

A Phase 2 study, sponsored by University of Washington.

Terminated
Registry status
Phase 2
Development phase
18
Enrollment target

NCT03442556: Clinical Trial Phase 2 study, sponsored by University of Washington.

NCT03442556 is a Phase 2 study that was terminated before completion, run by University of Washington. The registered enrollment target is 18 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (86% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03442556, a Phase 2 study, was terminated before completion, sponsored by University of Washington.

TERMINATED
Registry status
Phase 2
Development phase
18 participants
Enrollment target

Study Summary

This phase II trial studies how well docetaxel with carboplatin followed by rucaparib camsylate works in treating patients with metastatic castration resistant prostate cancer (spread outside of prostate and resistant to testosterone suppression) with homologous recombination DNA repair deficiency. Chemotherapy drugs, such as docetaxel and carboplatin, work to stop the growth of cancer cells, by stopping them from dividing or spreading. Rucaparib camsylate may stop the growth of tumor cells with defects in the ability to repair mistakes in DNA by forcing additional errors so that the cancer cells cannot overcome the number of errors and will then die. Giving induction docetaxel and carboplatin followed by maintenance rucaparib camsylate may work better in treating patients with castration resistant prostate cancer.

Primary Outcome

Radiologic progression free survival (rPFS) is defined as the time from first dose of docetaxel/carboplatin to the date of first objective evidence of radiographic progression (soft tissue or bone lesion) or death due to any cause, whichever occurs first. Radiographic disease progression includes confirmed bone disease progression and soft tissue disease progression adjudicated by investigator assessment using the RECIST 1.1/PCWG3 criteria.

Interventions

  • DRUG Carboplatin
  • DRUG Docetaxel
  • OTHER Laboratory Biomarker Analysis
  • DRUG Rucaparib
  • DRUG Rucaparib Camsylate

Trial Details

FieldValue
Enrollment Target 18 participants
Start Date 2018-08-24
Est. Completion 2025-06-04
Phase Phase 2
University of Washington

1,048 total trials

Why NCT03442556 stopped before completion

NCT03442556 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 18 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (86% lower).

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

NCT03442556 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03442556 about?

NCT03442556 is a clinical study titled "Docetaxel, Carboplatin, and Rucaparib Camsylate in Treating Patients With Metastatic Castration Resistant Prostate Cancer With Homologous Recombination DNA Repair Deficiency". This phase II trial studies how well docetaxel with carboplatin followed by rucaparib camsylate works in treating patients with metastatic castration resistant prostate cancer (spread outside of prostate and resistant to testosterone suppression) with homologous recombination DNA repair deficiency. ...

What is the current status of trial NCT03442556?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 18 participants. The study started on 2018-08-24. Estimated completion is 2025-06-04.

What interventions are being tested in trial NCT03442556?

The interventions under investigation include: Carboplatin (DRUG), Docetaxel (DRUG), Laboratory Biomarker Analysis (OTHER), Rucaparib (DRUG), Rucaparib Camsylate (DRUG).

Who is sponsoring clinical trial NCT03442556?

This trial is sponsored by University of Washington, which has 1,048 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03442556's enrollment target sits among peer trials

18 1898th of 2000 higher than 98 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03442556, the US trial registry maintained by the National Library of Medicine. NCT03442556 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.