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NCT00052065 · ClinicalTrials.gov registry record · Phase 1

TLK286 in Combination With Doxil in Platinum Refractory or Resistant Ovarian Cancer

A Phase 1 study, sponsored by Telik.

Completed
Registry status
Phase 1
Development phase
28
Enrollment target

NCT00052065: Completed Phase 1 study, sponsored by Telik.

NCT00052065 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.

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The verdict

NCT00052065, a Phase 1 study, has completed, sponsored by Telik.

COMPLETED
Registry status
Phase 1
Development phase
28 participants
Enrollment target

Study Summary

This is a dose-ranging, open-label, Phase 1-2a study of TLK286 in combination with Doxil in patients with platinum refractory or resistant ovarian cancer.

Interventions

  • DRUG TLK286

Trial Details

FieldValue
Enrollment Target 28 participants
Start Date 2003-02
Est. Completion 2006-03
Phase Phase 1
Telik

21 total trials

What the finished NCT00052065 record still lists

NCT00052065 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 is the first listed.

NCT00052065 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00052065 about?

NCT00052065 is a clinical study titled "TLK286 in Combination With Doxil in Platinum Refractory or Resistant Ovarian Cancer". This is a dose-ranging, open-label, Phase 1-2a study of TLK286 in combination with Doxil in patients with platinum refractory or resistant ovarian cancer.

What is the current status of trial NCT00052065?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 28 participants. The study started on 2003-02. Estimated completion is 2006-03.

What interventions are being tested in trial NCT00052065?

The interventions under investigation include: TLK286 (DRUG).

Who is sponsoring clinical trial NCT00052065?

This trial is sponsored by Telik, which has 21 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00052065'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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Source: ClinicalTrials.gov NCT00052065, the US trial registry maintained by the National Library of Medicine. NCT00052065 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.