Clinical trial
A Randomised, Double-blind Study to Determine the Safety and Efficacy of Iron Hydroxide Adipate Tartrate (IHAT) in Iron Deficient Premenopausal Women
NCT06285799 is registered in ClinicalTrials.gov with Nemysis Ltd as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Randomised, Double-blind Study to Determine the Safety and Efficacy of Iron Hydroxide Adipate Tartrate (IHAT) in Iron Deficient Premenopausal Women
- Lead sponsor
- Nemysis Ltd
- Phase
- Phase 3
- Overall status
- Completed
- Start date
- March 5, 2024
- Completion date
- February 15, 2025
- Enrollment
- 180 (actual)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.
iron-deficiency