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NCT04269707 · ClinicalTrials.gov registry record · Phase 3
Efficacy and Safety of Intravenous Ferric Carboxymaltose in Pediatric Patients With Iron Deficiency Anemia and Unsatisfactory Response Oral Iron Under Study Protocol 1VIT17044
A Phase 3 study of Iron Deficiency Anemia, sponsored by American Regent.
- Completed
- Registry status
- Phase 3
- Development phase
- 7
- Enrollment target
- 2
- Study locations
NCT04269707 is a Phase 3 study of Iron Deficiency Anemia that has completed, run by American Regent. The registered enrollment target is 7 participants, below the 193-participant average among 24 other Iron Deficiency Anemia trials with a reported enrollment target (96% lower). The trial reports 2 study locations across 1 state.
The verdict
NCT04269707, a Phase 3 study of Iron Deficiency Anemia, has completed, sponsored by American Regent.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 7 participants
- Enrollment target
- 2
- Study locations
Study Summary
Evaluating the Efficacy and Safety of Intravenous Ferric Carboxymaltose in Pediatric Patients with Iron Deficiency Anemia and an Unsatisfactory Response to Oral Iron under Study Protocol 1VIT17044
Conditions Studied
Interventions
- DRUG Ferric carboxymaltose
Study Locations (2)
Florida
- Miami Clinical Research - Miami
- South Florida Research Phase I-IV - Miami Springs
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 7 participants |
| Start Date | 2019-11-19 |
| Est. Completion | 2021-01-29 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04269707
The ClinicalTrials.gov registry entry for NCT04269707 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 7 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 193-participant average among 24 other Iron Deficiency Anemia trials with a reported enrollment target (96% lower). The listed sponsor is American Regent, which has 34 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Iron Deficiency Anemia appearing as the primary indexed condition, and to 1 intervention - of which Ferric carboxymaltose is the first listed.
NCT04269707 reports 2 study locations spanning 1 distinct geographic area - top geographies include Florida.
Frequently Asked Questions
What is clinical trial NCT04269707 about?
NCT04269707 is a clinical study titled "Efficacy and Safety of Intravenous Ferric Carboxymaltose in Pediatric Patients With Iron Deficiency Anemia and Unsatisfactory Response Oral Iron Under Study Protocol 1VIT17044". Evaluating the Efficacy and Safety of Intravenous Ferric Carboxymaltose in Pediatric Patients with Iron Deficiency Anemia and an Unsatisfactory Response to Oral Iron under Study Protocol 1VIT17044
What is the current status of trial NCT04269707?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 7 participants. The study started on 2019-11-19. Estimated completion is 2021-01-29.
What conditions does trial NCT04269707 study?
This clinical trial studies the following conditions: Iron Deficiency Anemia.
What interventions are being tested in trial NCT04269707?
The interventions under investigation include: Ferric carboxymaltose (DRUG).
Who is sponsoring clinical trial NCT04269707?
This trial is sponsored by American Regent, which has 34 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04269707 being conducted?
This trial has 2 study locations across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Iron Deficiency Anemia
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-
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-
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Read our methodology - how this data is sourced, computed, and verified.
Related
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