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NCT03827473 · ClinicalTrials.gov registry record · Phase 2

Docetaxel or Abiraterone Acetate With ADT in Treating Patients With Metastatic Hormone Sensitive Prostate Cancer

A Phase 2 study, sponsored by University of Utah.

Terminated
Registry status
Phase 2
Development phase
1
Enrollment target

NCT03827473: Clinical Trial Phase 2 study, sponsored by University of Utah.

NCT03827473 is a Phase 2 study that was terminated before completion, run by University of Utah. The registered enrollment target is 1 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03827473, a Phase 2 study, was terminated before completion, sponsored by University of Utah.

TERMINATED
Registry status
Phase 2
Development phase
1 participants
Enrollment target

Study Summary

This phase II trial studies how well docetaxel or abiraterone acetate work when combined with androgen deprivation therapy (ADT) in treating patients with hormone sensitive prostate cancer that has spread to other parts of the body. Drugs used in chemotherapy, such as docetaxel and abiraterone acetate, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Antihormone therapy, such as ADT may lessen the amount of androgen made by the body. It is not yet known whether docetaxel or abiraterone acetate work better when combined with ADT in treating patients with hormone sensitive prostate cancer.

Primary Outcome

The impact of abiraterone acetate and docetaxel on health related quality of life will be assessed every 3 months from screening to month 12 of treatment or follow-up. The scale used will be the Functional Assessment of Cancer Therapy-Prostate (FACT-P) scale. The total score ranges from 0 to 156, with higher scores indicating a higher quality of life. The primary endpoint was intended to be quality of life at 12 months, but since no participants completed 12 months of treatment/follow-up, scores

Interventions

  • DRUG Docetaxel
  • OTHER Quality-of-Life Assessment
  • DRUG Antiandrogen Therapy
  • DRUG Prednisone
  • DRUG Abiraterone Acetate

Trial Details

FieldValue
Enrollment Target 1 participants
Start Date 2019-02-08
Est. Completion 2019-07-31
Phase Phase 2
University of Utah

818 total trials

Why NCT03827473 stopped before completion

NCT03827473 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 1 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (99% lower).

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

NCT03827473 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03827473 about?

NCT03827473 is a clinical study titled "Docetaxel or Abiraterone Acetate With ADT in Treating Patients With Metastatic Hormone Sensitive Prostate Cancer". This phase II trial studies how well docetaxel or abiraterone acetate work when combined with androgen deprivation therapy (ADT) in treating patients with hormone sensitive prostate cancer that has spread to other parts of the body. Drugs used in chemotherapy, such as docetaxel and abiraterone aceta...

What is the current status of trial NCT03827473?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 1 participants. The study started on 2019-02-08. Estimated completion is 2019-07-31.

What interventions are being tested in trial NCT03827473?

The interventions under investigation include: Docetaxel (DRUG), Quality-of-Life Assessment (OTHER), Antiandrogen Therapy (DRUG), Prednisone (DRUG), Abiraterone Acetate (DRUG).

Who is sponsoring clinical trial NCT03827473?

This trial is sponsored by University of Utah, which has 818 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03827473's enrollment target sits among peer trials

1 2001st of 2000 the lowest 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 NCT03827473, the US trial registry maintained by the National Library of Medicine. NCT03827473 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.