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Phase 3Heart FailureCurrently Recruiting

P-Monofer-CHF-02 — Ferric Derisomaltose

Iron-Deficient Chronic Heart Failure

Sponsor: Pharmacosmos · P-Monofer-CHF-02

About this study

Phase 3 evaluation of intravenous ferric derisomaltose (Monofer) in patients with chronic heart failure and iron deficiency.

To evaluate whether intravenous iron replacement improves cardiovascular outcomes and quality of life in adults with chronic heart failure and iron deficiency.

Study details

Sponsor
Pharmacosmos
Protocol
P-Monofer-CHF-02
Phase
Phase 3
Indication
Iron-Deficient Chronic Heart Failure
Status
Currently Recruiting

High-level eligibility

  • Adults with HFrEF or HFpEF
  • Confirmed iron deficiency (TSAT <20% or ferritin criteria)
  • Stable on guideline-directed therapy

Eligibility above is a summary. Final qualification is determined by the study protocol and a screening visit at amavita Heart and Vascular Health®.

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Participation in any clinical trial is voluntary and requires written informed consent reviewed by an Institutional Review Board (IRB) before any study procedure. You may withdraw at any time. Website content is informational and is not a substitute for medical advice from a licensed clinician.