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NCT00112684 · ClinicalTrials.gov registry record · Phase 1

Alvocidib in Treating Patients With Locally Advanced or Metastatic Solid Tumors

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

Terminated
Registry status
Phase 1
Development phase
25
Enrollment target

NCT00112684: Clinical Trial Phase 1 study, sponsored by National Cancer Institute (NCI).

NCT00112684 is a Phase 1 study that was terminated before completion, run by National Cancer Institute (NCI). The registered enrollment target is 25 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (58% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00112684, a Phase 1 study, was terminated before completion, sponsored by National Cancer Institute (NCI).

TERMINATED
Registry status
Phase 1
Development phase
25 participants
Enrollment target

Study Summary

This phase I trial is studying the side effects and best dose of alvocidib in treating patients with locally advanced or metastatic solid tumors. Drugs used in chemotherapy, such as alvocidib, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Alvocidib may also stimulate the immune system in different ways and stop tumor cells from growing. It may also stop the growth of solid tumors by blocking blood flow to the tumor.

Primary Outcome

Graded using the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version 3.0.

Interventions

  • OTHER laboratory biomarker analysis
  • OTHER pharmacological study
  • DRUG alvocidib

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2006-02
Phase Phase 1
National Cancer Institute (NCI)

3,257 total trials

Why NCT00112684 stopped before completion

NCT00112684 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 25 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (58% lower).

The record links to 0 conditions, and to 3 interventions - of which laboratory biomarker analysis is the first listed.

NCT00112684 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00112684 about?

NCT00112684 is a clinical study titled "Alvocidib in Treating Patients With Locally Advanced or Metastatic Solid Tumors". This phase I trial is studying the side effects and best dose of alvocidib in treating patients with locally advanced or metastatic solid tumors. Drugs used in chemotherapy, such as alvocidib, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them f...

What is the current status of trial NCT00112684?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 25 participants. The study started on 2006-02.

What interventions are being tested in trial NCT00112684?

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

Who is sponsoring clinical trial NCT00112684?

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 NCT00112684's enrollment target sits among peer trials

25 1495th of 2000 higher than 481 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 NCT00112684, the US trial registry maintained by the National Library of Medicine. NCT00112684 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.