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NCT00287937 · ClinicalTrials.gov registry record · Phase 1

Vorinostat, Paclitaxel, and Carboplatin in Treating Patients With Advanced or Refractory Solid Tumors

A Phase 1 study, sponsored by National Cancer Institute (NCI).

Completed
Registry status
Phase 1
Development phase
30
Enrollment target

NCT00287937: Completed Phase 1 study, sponsored by National Cancer Institute (NCI).

NCT00287937 is a Phase 1 study that has completed, run by National Cancer Institute (NCI). The registered enrollment target is 30 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (50% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00287937, a Phase 1 study, has completed, sponsored by National Cancer Institute (NCI).

COMPLETED
Registry status
Phase 1
Development phase
30 participants
Enrollment target

Study Summary

This phase I trial is studying the side effects and best dose of vorinostat when given together with paclitaxel and carboplatin in treating patients with advanced or refractory solid tumors. Vorinostat may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as paclitaxel and carboplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving vorinostat together with paclitaxel and carboplatin may kill more tumor cells

Interventions

  • OTHER laboratory biomarker analysis
  • DRUG carboplatin
  • DRUG vorinostat
  • DRUG paclitaxel
  • OTHER pharmacological study

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2005-07
Phase Phase 1
National Cancer Institute (NCI)

3,257 total trials

What the finished NCT00287937 record still lists

NCT00287937 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (50% lower).

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

NCT00287937 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00287937 about?

NCT00287937 is a clinical study titled "Vorinostat, Paclitaxel, and Carboplatin in Treating Patients With Advanced or Refractory Solid Tumors". This phase I trial is studying the side effects and best dose of vorinostat when given together with paclitaxel and carboplatin in treating patients with advanced or refractory solid tumors. Vorinostat may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs u...

What is the current status of trial NCT00287937?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 30 participants. The study started on 2005-07.

What interventions are being tested in trial NCT00287937?

The interventions under investigation include: laboratory biomarker analysis (OTHER), carboplatin (DRUG), vorinostat (DRUG), paclitaxel (DRUG), pharmacological study (OTHER).

Who is sponsoring clinical trial NCT00287937?

This trial is sponsored by National Cancer Institute (NCI), which has 3,257 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00287937's enrollment target sits among peer trials

30 1332nd of 2000 higher than 561 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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 NCT00287937, the US trial registry maintained by the National Library of Medicine. NCT00287937 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.