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NCT00450970 · ClinicalTrials.gov registry record · Phase 3
Expanded Access Study of Satraplatin Plus Prednisone in Patients With Hormone Refractory Prostate Cancer (HRPC)
A Phase 3 study, sponsored by Agennix.
- Terminated
- Registry status
- Phase 3
- Development phase
- 344
- Enrollment target
NCT00450970: Clinical Trial Phase 3 study, sponsored by Agennix.
NCT00450970 is a Phase 3 study that was terminated before completion, run by Agennix. The registered enrollment target is 344 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (55% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00450970, a Phase 3 study, was terminated before completion, sponsored by Agennix.
- TERMINATED
- Registry status
- Phase 3
- Development phase
- 344 participants
- Enrollment target
Study Summary
The SPERA trial is designed to 1. provide satraplatin to physicians with patients who have hormone refractory prostate cancer (HRPC) which has progressed following unlimited cytotoxic chemotherapy regimens for metastatic disease and 2. to evaluate the safety of oral satraplatin in this patient population.
Interventions
- DRUG Oral Satraplatin
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 344 participants |
| Start Date | 2007-02 |
| Est. Completion | 2009-12 |
| Phase | Phase 3 |
Why NCT00450970 stopped before completion
NCT00450970 is an interventional study that assigns participants to a tested intervention. The registered 344 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 (55% lower).
The record links to 0 conditions, and to 1 intervention - of which Oral Satraplatin is the first listed.
NCT00450970 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00450970 about?
NCT00450970 is a clinical study titled "Expanded Access Study of Satraplatin Plus Prednisone in Patients With Hormone Refractory Prostate Cancer (HRPC)". The SPERA trial is designed to 1. provide satraplatin to physicians with patients who have hormone refractory prostate cancer (HRPC) which has progressed following unlimited cytotoxic chemotherapy regimens for metastatic disease and 2. to evaluate the safety of oral satraplatin in this patient popul...
What is the current status of trial NCT00450970?
This trial is currently terminated. It is a Phase 3 study. The enrollment target is 344 participants. The study started on 2007-02. Estimated completion is 2009-12.
What interventions are being tested in trial NCT00450970?
The interventions under investigation include: Oral Satraplatin (DRUG).
Who is sponsoring clinical trial NCT00450970?
This trial is sponsored by Agennix, which has 13 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00450970's enrollment target sits among peer trials
344 1050th of 2000 higher than 950 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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