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NCT00103272 · ClinicalTrials.gov registry record · Phase 1

17-N-Allylamino-17-Demethoxygeldanamycin and Bortezomib in Treating Patients With Relapsed or Refractory Hematologic Cancer

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

Terminated
Registry status
Phase 1
Development phase
74
Enrollment target

NCT00103272: Clinical Trial Phase 1 study, sponsored by National Cancer Institute (NCI).

NCT00103272 is a Phase 1 study that was terminated before completion, run by National Cancer Institute (NCI). The registered enrollment target is 74 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (23% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00103272, a Phase 1 study, was terminated before completion, sponsored by National Cancer Institute (NCI).

TERMINATED
Registry status
Phase 1
Development phase
74 participants
Enrollment target

Study Summary

This phase I trial is studying the side effects and best dose of 17-N-allylamino-17-demethoxygeldanamycin and bortezomib in treating patients with relapsed or refractory hematologic cancer. Drugs used in chemotherapy, such as 17-N-allylamino-17-demethoxygeldanamycin, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Bortezomib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Giving 17-N-allylamino-17-demethoxygeldanamycin together with bortezomib may kill more cancer cells.

Primary Outcome

Defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity.

Interventions

  • DRUG bortezomib
  • DRUG tanespimycin

Trial Details

FieldValue
Enrollment Target 74 participants
Start Date 2005-04
Phase Phase 1
National Cancer Institute (NCI)

3,257 total trials

Why NCT00103272 stopped before completion

NCT00103272 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 74 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (23% higher).

The record links to 0 conditions, and to 2 interventions - of which bortezomib is the first listed.

NCT00103272 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00103272 about?

NCT00103272 is a clinical study titled "17-N-Allylamino-17-Demethoxygeldanamycin and Bortezomib in Treating Patients With Relapsed or Refractory Hematologic Cancer". This phase I trial is studying the side effects and best dose of 17-N-allylamino-17-demethoxygeldanamycin and bortezomib in treating patients with relapsed or refractory hematologic cancer. Drugs used in chemotherapy, such as 17-N-allylamino-17-demethoxygeldanamycin, work in different ways to stop t...

What is the current status of trial NCT00103272?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 74 participants. The study started on 2005-04.

What interventions are being tested in trial NCT00103272?

The interventions under investigation include: bortezomib (DRUG), tanespimycin (DRUG).

Who is sponsoring clinical trial NCT00103272?

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 NCT00103272's enrollment target sits among peer trials

74 725th of 2000 higher than 1,269 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 NCT00103272, the US trial registry maintained by the National Library of Medicine. NCT00103272 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.