Status:

NO_LONGER_AVAILABLE

A Single-patient Study of Repeat-dose Administration of Prometic Plasminogen (Human) Intravenous

Lead Sponsor:

Prometic Biotherapeutics, Inc.

Collaborating Sponsors:

Cedars-Sinai Medical Center

Vanderbilt University Medical Center

Conditions:

Hypoplasminogenemia

Eligibility:

All Genders

16+ years

Brief Summary

These are single-patient studies with repeat-dose administration of ProMetic Plasminogen IV infusion in one adult and one child with hypoplasminogenemia. These patients are under treatment to address ...

Eligibility Criteria

Inclusion

  • Patient has provided informed consent.
  • Patient has a diagnosis of compound homozygous Type 1 plasminogen deficiency as evidence by ligneous conjunctivitis since birth as well as involvement of the conjunctiva, nasopharynx, gingiva, tracheobronchial tree, gastrointestinal tract, and urinary tract.

Exclusion

  • Not applicable

Key Trial Info

Start Date :

Trial Type :

EXPANDED_ACCESS

End Date :

Estimated Enrollment :

Patients enrolled

Trial Details

Trial ID

NCT03265171

Last Update

April 24 2020

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