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NCT00087217 · ClinicalTrials.gov registry record · Phase 1

17-N-Allylamino-17-Demethoxygeldanamycin and Paclitaxel in Treating Patients With Metastatic or Unresectable Solid Tumor

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

Completed
Registry status
Phase 1
Development phase
35
Enrollment target

NCT00087217: Completed Phase 1 study, sponsored by National Cancer Institute (NCI).

NCT00087217 is a Phase 1 study that has completed, run by National Cancer Institute (NCI). The registered enrollment target is 35 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (42% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00087217, a Phase 1 study, has completed, sponsored by National Cancer Institute (NCI).

COMPLETED
Registry status
Phase 1
Development phase
35 participants
Enrollment target

Study Summary

This phase I trial is studying the side effects and best dose of 17-N-allylamino-17-demethoxygeldanamycin when given together with paclitaxel in treating patients with metastatic or unresectable solid tumor. Drugs used in chemotherapy, such as 17-N-allylamino-17-demethoxygeldanamycin and paclitaxel, work in different ways to stop tumor cells from dividing so they stop growing or die. Combining 17-N-allylamino-17-demethoxygeldanamycin with paclitaxel may kill more tumor cells

Primary Outcome

Tabulated according to the NCI CTC.

Interventions

  • OTHER laboratory biomarker analysis
  • DRUG paclitaxel
  • OTHER pharmacological study
  • DRUG tanespimycin

Trial Details

FieldValue
Enrollment Target 35 participants
Start Date 2004-05
Phase Phase 1
National Cancer Institute (NCI)

3,257 total trials

What the finished NCT00087217 record still lists

NCT00087217 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 35 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (42% lower).

The record links to 0 conditions, and to 4 interventions - of which laboratory biomarker analysis is the first listed.

NCT00087217 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00087217 about?

NCT00087217 is a clinical study titled "17-N-Allylamino-17-Demethoxygeldanamycin and Paclitaxel in Treating Patients With Metastatic or Unresectable Solid Tumor". This phase I trial is studying the side effects and best dose of 17-N-allylamino-17-demethoxygeldanamycin when given together with paclitaxel in treating patients with metastatic or unresectable solid tumor. Drugs used in chemotherapy, such as 17-N-allylamino-17-demethoxygeldanamycin and paclitaxel,...

What is the current status of trial NCT00087217?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 35 participants. The study started on 2004-05.

What interventions are being tested in trial NCT00087217?

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

Who is sponsoring clinical trial NCT00087217?

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 NCT00087217's enrollment target sits among peer trials

35 1258th of 2000 higher than 728 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 NCT00087217, the US trial registry maintained by the National Library of Medicine. NCT00087217 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.