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NCT00317239 · ClinicalTrials.gov registry record · Phase 3
VIT45 Versus Oral Iron in the Treatment of Anemia in Non-Dialysis Dependent Chronic Kidney Disease
A Phase 3 study, sponsored by American Regent.
- Completed
- Registry status
- Phase 3
- Development phase
- 255
- Enrollment target
NCT00317239 is a Phase 3 study that has completed, run by American Regent. The registered enrollment target is 255 participants.
The verdict
NCT00317239, a Phase 3 study, has completed, sponsored by American Regent.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 255 participants
- Enrollment target
Study Summary
This study compares the efficacy and safety of intravenous (IV) iron (VIT45) versus oral iron (ferrous sulfate) administered to subjects who suffer from anemia and are diagnosed with non-dialysis dependent chronic kidney disease (NDD-CKD).
Interventions
- DRUG Ferric Carboxymaltose (FCM)
- DRUG Ferrous Sulfate tablets
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 255 participants |
| Start Date | 2005-05 |
| Est. Completion | 2007-08 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00317239
The ClinicalTrials.gov registry entry for NCT00317239 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 255 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is American Regent, which has 34 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Ferric Carboxymaltose (FCM) is the first listed.
NCT00317239 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00317239 about?
NCT00317239 is a clinical study titled "VIT45 Versus Oral Iron in the Treatment of Anemia in Non-Dialysis Dependent Chronic Kidney Disease". This study compares the efficacy and safety of intravenous (IV) iron (VIT45) versus oral iron (ferrous sulfate) administered to subjects who suffer from anemia and are diagnosed with non-dialysis dependent chronic kidney disease (NDD-CKD).
What is the current status of trial NCT00317239?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 255 participants. The study started on 2005-05. Estimated completion is 2007-08.
What interventions are being tested in trial NCT00317239?
The interventions under investigation include: Ferric Carboxymaltose (FCM) (DRUG), Ferrous Sulfate tablets (DRUG).
Who is sponsoring clinical trial NCT00317239?
This trial is sponsored by American Regent, which has 34 total clinical trials registered on ClinicalTrials.gov.
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