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NCT00112723 · ClinicalTrials.gov registry record · Phase 1

Flavopiridol in Treating Patients With Relapsed or Refractory Lymphoma or Multiple Myeloma

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

Terminated
Registry status
Phase 1
Development phase
46
Enrollment target

NCT00112723: Clinical Trial Phase 1 study, sponsored by National Cancer Institute (NCI).

NCT00112723 is a Phase 1 study that was terminated before completion, run by National Cancer Institute (NCI). The registered enrollment target is 46 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (23% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00112723, a Phase 1 study, was terminated before completion, sponsored by National Cancer Institute (NCI).

TERMINATED
Registry status
Phase 1
Development phase
46 participants
Enrollment target

Study Summary

This phase I/II trial is studying the side effects and best dose of flavopiridol and to see how well it works in treating patients with lymphoma or multiple myeloma. Drugs used in chemotherapy, such as flavopiridol, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing.

Primary Outcome

Dose limiting toxicity (DLT) for an individual disease group is defined as 1) any grade 3-4 non-hematologic toxicity (except leukopenia or neutropenia) that does not resolve or decrease to grade 1-2 within 2 weeks, or 2) any grade 4 hematologic toxicity that causes more than a 1 week delay in administration of therapy.

Interventions

  • DRUG alvocidib

Trial Details

FieldValue
Enrollment Target 46 participants
Start Date 2005-12
Est. Completion 2015-11
Phase Phase 1
National Cancer Institute (NCI)

3,257 total trials

Why NCT00112723 stopped before completion

NCT00112723 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 46 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (23% lower).

The record links to 0 conditions, and to 1 intervention - of which alvocidib is the first listed.

NCT00112723 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00112723 about?

NCT00112723 is a clinical study titled "Flavopiridol in Treating Patients With Relapsed or Refractory Lymphoma or Multiple Myeloma". This phase I/II trial is studying the side effects and best dose of flavopiridol and to see how well it works in treating patients with lymphoma or multiple myeloma. Drugs used in chemotherapy, such as flavopiridol, work in different ways to stop the growth of cancer cells, either by killing the cel...

What is the current status of trial NCT00112723?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 46 participants. The study started on 2005-12. Estimated completion is 2015-11.

What interventions are being tested in trial NCT00112723?

The interventions under investigation include: alvocidib (DRUG).

Who is sponsoring clinical trial NCT00112723?

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 NCT00112723's enrollment target sits among peer trials

46 1058th of 2000 higher than 935 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 NCT00112723, the US trial registry maintained by the National Library of Medicine. NCT00112723 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.