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NCT00703937 · ClinicalTrials.gov registry record · Phase 3
Safety and Tolerability of Ferric Carboxymaltose (FCM) Versus Standard of Care in Treating Iron Deficiency Anemia
A Phase 3 study, sponsored by American Regent.
- Completed
- Registry status
- Phase 3
- Development phase
- 708
- Enrollment target
NCT00703937 is a Phase 3 study that has completed, run by American Regent. The registered enrollment target is 708 participants.
The verdict
NCT00703937, a Phase 3 study, has completed, sponsored by American Regent.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 708 participants
- Enrollment target
Study Summary
The objective of this study is to evaluate the safety of FCM in patients with anemia who are not dialysis dependent.
Interventions
- DRUG Ferric Carboxymaltose (FCM)
- DRUG Standard Medical Care (SMC) for the treatment of IDA
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 708 participants |
| Start Date | 2008-07 |
| Est. Completion | 2011-03 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00703937
The ClinicalTrials.gov registry entry for NCT00703937 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 708 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.
NCT00703937 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00703937 about?
NCT00703937 is a clinical study titled "Safety and Tolerability of Ferric Carboxymaltose (FCM) Versus Standard of Care in Treating Iron Deficiency Anemia". The objective of this study is to evaluate the safety of FCM in patients with anemia who are not dialysis dependent.
What is the current status of trial NCT00703937?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 708 participants. The study started on 2008-07. Estimated completion is 2011-03.
What interventions are being tested in trial NCT00703937?
The interventions under investigation include: Ferric Carboxymaltose (FCM) (DRUG), Standard Medical Care (SMC) for the treatment of IDA (DRUG).
Who is sponsoring clinical trial NCT00703937?
This trial is sponsored by American Regent, which has 34 total clinical trials registered on ClinicalTrials.gov.
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