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NCT00058253 · ClinicalTrials.gov registry record · Phase 1
Combination Chemotherapy in Treating Patients With Metastatic or Unresectable Solid Tumors
A Phase 1 study of Unspecified Adult Solid Tumor, Protocol Specific and Recurrent Prostate Cancer, sponsored by National Cancer Institute (NCI).
- Completed
- Registry status
- Phase 1
- Development phase
- 80
- Enrollment target
- 1
- Study location
NCT00058253: Completed Phase 1 study of Unspecified Adult Solid Tumor, Protocol Specific and Recurrent Prostate Cancer, sponsored by National Cancer Institute (NCI).
NCT00058253 is a Phase 1 study of Unspecified Adult Solid Tumor, Protocol Specific and Recurrent Prostate Cancer that has completed, run by National Cancer Institute (NCI). The registered enrollment target is 80 participants, below the 500-participant average among 83 other Unspecified Adult Solid Tumor, Protocol Specific trials with a reported enrollment target (84% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00058253, a Phase 1 study of Unspecified Adult Solid Tumor, Protocol Specific and Recurrent Prostate Cancer, has completed, sponsored by National Cancer Institute (NCI).
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 80 participants
- Enrollment target
- 1
- Study location
Study Summary
This phase I trial is studying the side effects and best dose of combination chemotherapy in treating patients with metastatic or unresectable solid tumors. Drugs used in chemotherapy, such as docetaxel and 17-N-allylamino-17-demethoxygeldanamycin, work in different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells.
Conditions Studied
Interventions
- DRUG docetaxel
- DRUG tanespimycin
Study Locations (1)
New York
- Memorial Sloan-Kettering Cancer Center - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 80 participants |
| Start Date | 2003-02 |
| Est. Completion | 2010-03 |
| Phase | Phase 1 |
What the finished NCT00058253 record still lists
NCT00058253 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 80 participants, a relatively small participant target, below the 500-participant average among 83 other Unspecified Adult Solid Tumor, Protocol Specific trials with a reported enrollment target (84% lower).
The record links to 3 conditions, with Unspecified Adult Solid Tumor, Protocol Specific appearing as the primary indexed condition, and to 2 interventions - of which docetaxel is the first listed.
NCT00058253 reports a single indexed study location in New York.
Frequently Asked Questions
What is clinical trial NCT00058253 about?
NCT00058253 is a clinical study titled "Combination Chemotherapy in Treating Patients With Metastatic or Unresectable Solid Tumors". This phase I trial is studying the side effects and best dose of combination chemotherapy in treating patients with metastatic or unresectable solid tumors. Drugs used in chemotherapy, such as docetaxel and 17-N-allylamino-17-demethoxygeldanamycin, work in different ways to stop tumor cells from div...
What is the current status of trial NCT00058253?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 80 participants. The study started on 2003-02. Estimated completion is 2010-03.
What conditions does trial NCT00058253 study?
This clinical trial studies the following conditions: Unspecified Adult Solid Tumor, Protocol Specific, Recurrent Prostate Cancer, Stage IV Prostate Cancer.
What interventions are being tested in trial NCT00058253?
The interventions under investigation include: docetaxel (DRUG), tanespimycin (DRUG).
Who is sponsoring clinical trial NCT00058253?
This trial is sponsored by National Cancer Institute (NCI), which has 3,257 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00058253 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Unspecified Adult Solid Tumor, Protocol Specific
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT00058253's enrollment target sits among peer trials
80 21st of 83 higher than 63 of 83 other Unspecified Adult Solid Tumor, Protocol Specific trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Unspecified Adult Solid Tumor, Protocol Specific 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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