At a glance
ClinicalIndex Comparison RecordPhase 1Completed· 14 enrolled
Drug / intervention
Triferic +2 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Pharmacokinetics and Absolute Bioavailability of Fer-In-Sol (Ferrous Sulfate) and Triferic (Ferric Pyrophosphate Citrate) Administered Orally With Shohl's Solution in Healthy Volunteers
In Brief
A Phase 1 clinical trial evaluating Triferic, Fer-In-Sol, and 1 other intervention for Iron-refractory, Iron-deficiency Anemia (IRIDA). Completed, enrolled 14 participants across 1 site.
Detailed Summary
The main purpose is to determine the pharmacokinetics (PK) of Triferic iron administered orally in healthy adult volunteers. It is a randomized multiple treatments, single dose study.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--
Timeline
Phase 1CompletedFinished
20162017201820192020202120222023202420252026
Enrollment StartApr 2016
Primary CompletionApr 2016
First PostedMay 2016
TodayJul 2026
First PostedMay 10, 2016
Enrollment StartApr 1, 2016
Primary CompletionApr 1, 2016
TodayJul 2, 2026
Enrollment to primary: 0 daysPosted 10.1 years ago
Interventions
Trifericdrug
Fer-In-Soldrug
Shohl's solutiondrug