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

NCT03265171 · Status: NO_LONGER_AVAILABLE · Type: EXPANDED_ACCESS

Last updated 2020-04-24

No results posted yet for this study

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 wound healing and obstructions.

Conditions

  • Hypoplasminogenemia

Interventions

BIOLOGICAL

Plasminogen (Human)

Sponsors & Collaborators

  • Cedars-Sinai Medical Center

    collaborator OTHER
  • Vanderbilt University Medical Center

    collaborator OTHER
  • Indiana Hemophilia &Thrombosis Center, Inc.

    collaborator OTHER
  • Prometic Biotherapeutics, Inc.

    lead INDUSTRY

Eligibility

Min Age
16 Months
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03265171 on ClinicalTrials.gov