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NCT00047801 · ClinicalTrials.gov registry record · Phase 1
Phase 1-2a Dose-Ranging Study of TLK286 in Combination With Docetaxel in Platinum-Resistant Non-Small Cell Lung Cancer
A Phase 1 study, sponsored by Telik.
- Completed
- Registry status
- Phase 1
- Development phase
- 28
- Enrollment target
NCT00047801: Completed Phase 1 study, sponsored by Telik.
NCT00047801 is a Phase 1 study that has completed, run by Telik. The registered enrollment target is 28 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (53% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00047801, a Phase 1 study, has completed, sponsored by Telik.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 28 participants
- Enrollment target
Study Summary
The purpose of this study is to determine the effectiveness and safety of TLK286 given intravenously once every three weeks in combination with docetaxel (Taxotere) in the treatment of patients with non-small cell lung cancer that is resistant to platinum-based chemotherapy.
Interventions
- DRUG TLK286 in combination with docetaxel
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 28 participants |
| Start Date | 2002-10 |
| Est. Completion | 2004-09 |
| Phase | Phase 1 |
What the finished NCT00047801 record still lists
NCT00047801 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 28 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (53% lower).
The record links to 0 conditions, and to 1 intervention - of which TLK286 in combination with docetaxel is the first listed.
NCT00047801 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00047801 about?
NCT00047801 is a clinical study titled "Phase 1-2a Dose-Ranging Study of TLK286 in Combination With Docetaxel in Platinum-Resistant Non-Small Cell Lung Cancer". The purpose of this study is to determine the effectiveness and safety of TLK286 given intravenously once every three weeks in combination with docetaxel (Taxotere) in the treatment of patients with non-small cell lung cancer that is resistant to platinum-based chemotherapy.
What is the current status of trial NCT00047801?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 28 participants. The study started on 2002-10. Estimated completion is 2004-09.
What interventions are being tested in trial NCT00047801?
The interventions under investigation include: TLK286 in combination with docetaxel (DRUG).
Who is sponsoring clinical trial NCT00047801?
This trial is sponsored by Telik, which has 21 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00047801's enrollment target sits among peer trials
28 1447th of 2000 higher than 538 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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