A Study to Evaluate BBI-001 in Hereditary Haemochromatosis (HH) Patients and Iron Deficient Volunteers

  • participants needed
  • sponsor
    Bond Biosciences
Updated on 28 November 2022
Accepts healthy volunteers


This is a first in human, double-blind, randomized, placebo-controlled, two-arm crossover study evaluating the safety, tolerability and PD of ascending dose levels of BBI-001 after:

  • a single administration in iron deficient male and female participants, and male and female HH patients (Part A),
  • two administrations per day in HH patients (Part B). BBI-001 administrations will be accompanied with consumption of a meal enriched with stable iron isotope Fe57, while corresponding placebo dose administrations will be with a meal enriched with stable iron isotope Fe58.

Condition Hereditary Hemochromatosis
Treatment BBI-001, Original Fibre Metamucil
Clinical Study IdentifierNCT05238207
SponsorBond Biosciences
Last Modified on28 November 2022

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