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NCT00350948 · ClinicalTrials.gov registry record · Phase 3
Phase 3 Randomized Study of Telcyta + Doxorubicin Versus Doxorubicin in Platinum Refractory or Resistant Ovarian Cancer
A Phase 3 study, sponsored by Telik.
- Terminated
- Registry status
- Phase 3
- Development phase
- 244
- Enrollment target
NCT00350948: Clinical Trial Phase 3 study, sponsored by Telik.
NCT00350948 is a Phase 3 study that was terminated before completion, run by Telik. The registered enrollment target is 244 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (68% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00350948, a Phase 3 study, was terminated before completion, sponsored by Telik.
- TERMINATED
- Registry status
- Phase 3
- Development phase
- 244 participants
- Enrollment target
Study Summary
The purpose of this research study is to determine if Telcyta® given in combination with liposomal doxorubicin is more effective than liposomal doxorubicin alone in treating women who have recurrent ovarian epithelial cancer, fallopian tube cancer or primary peritoneal cancer that is refractory or resistant to platinum chemotherapy.
Interventions
- DRUG Liposomal Doxorubicin
- DRUG Telcyta
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 244 participants |
| Start Date | 2006-05 |
| Est. Completion | 2008-12 |
| Phase | Phase 3 |
Why NCT00350948 stopped before completion
NCT00350948 is an interventional study that assigns participants to a tested intervention. The registered 244 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (68% lower).
The record links to 0 conditions, and to 2 interventions - of which Liposomal Doxorubicin is the first listed.
NCT00350948 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00350948 about?
NCT00350948 is a clinical study titled "Phase 3 Randomized Study of Telcyta + Doxorubicin Versus Doxorubicin in Platinum Refractory or Resistant Ovarian Cancer". The purpose of this research study is to determine if Telcyta® given in combination with liposomal doxorubicin is more effective than liposomal doxorubicin alone in treating women who have recurrent ovarian epithelial cancer, fallopian tube cancer or primary peritoneal cancer that is refractory or r...
What is the current status of trial NCT00350948?
This trial is currently terminated. It is a Phase 3 study. The enrollment target is 244 participants. The study started on 2006-05. Estimated completion is 2008-12.
What interventions are being tested in trial NCT00350948?
The interventions under investigation include: Liposomal Doxorubicin (DRUG), Telcyta (DRUG).
Who is sponsoring clinical trial NCT00350948?
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 NCT00350948's enrollment target sits among peer trials
244 1269th of 2000 higher than 732 of 2,000 other Phase 3 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 3 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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