Ferric maltol

(Accrufer®)

Accrufer®

Drug updated on 10/29/2024

Dosage FormCapsule (oral; 30 mg)
Drug ClassIron replacement products
Ongoing and
Completed Studies
ClinicalTrials.gov

Indication

  • Indicated for the treatment of iron deficiency in adults.

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Summary
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  • This summary is based on the review of one systematic review(s)/meta-analysis(es). [1]
  • Intravenous ferric carboxymaltose is probably superior to intravenous iron sucrose for increasing hemoglobin by 20 g/L or 10 g/L (Relative Risk 1.25, 95% Confidence Interval 1.06 to 1.46, Number Needed to Treat for Benefit = 9).
  • Oral ferric maltol shows superiority over placebo for increasing hemoglobin levels (Relative Risk 73.00, 95% Confidence Interval 4.58 to 1164.36).
  • Intravenous iron preparations may lead to more responders compared to oral iron (Relative Risk 1.17, 95% Confidence Interval 1.05 to 1.31, Number Needed to Treat for Benefit = 11), with fewer withdrawals due to adverse events (Relative Risk 0.39, 95% Confidence Interval 0.20 to 0.74).
  • No significant differences in serious adverse events or therapy withdrawals were found between the studied intervention agents; however, the certainty of these findings is very low due to risk of bias and imprecision.
  • Withdrawals due to adverse events may be greater with oral iron preparations compared to intravenous iron (15/554 vs. 31/373, Relative Risk 0.39, 95% Confidence Interval 0.20 to 0.74, low-certainty).
  • There is no population types or subgroups information available in the reviewed studies.

Product Monograph / Prescribing Information

Document TitleYearSource
Accrufer (ferric maltol) Prescribing Information.2023Shield Therapeutics Inc, North Austin, TX

Systematic Reviews / Meta-Analyses

Document TitleYearSource
Interventions for treating iron deficiency anaemia in inflammatory bowel disease2021The Cochrane Database of Systematic Reviews

Clinical Practice Guidelines