Apotransferrin in Atransferrinemia

  • STATUS
    Recruiting
  • End date
    Jan 8, 2024
  • participants needed
    10
  • sponsor
    Prothya Biosolutions
Updated on 8 December 2021

Summary

Atransferrinemia is a very rare disorder, which is caused by a deficiency of the protein transferrin. No regular treatment is available for these patients. The objective of this study is to investigate the pharmacokinetics, efficacy and safety of Apotransferrin replacement therapy in atransferrinemia patients.

Details
Condition Congenital Atransferrinemia
Treatment Human apotransferrin
Clinical Study IdentifierNCT01797055
SponsorProthya Biosolutions
Last Modified on8 December 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Established diagnosis of atransferrinemia, defined as serum levels of transferrin below 40 mg/dl
Informed consent

Exclusion Criteria

Known with allergic reactions against human plasma or plasma products
Having detectable anti-immunoglobulin A antibodies
Clear my responses

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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