Overview

Safety, Pharmacokinetics and Efficacy of an AT-III Concentrate.

Status:
Active, not recruiting
Trial end date:
2029-03-01
Target enrollment:
Participant gender:
Summary
To assess the safety, pharmacokinetics and efficacy of a plasma-derived AT-III concentrate in the treatment of subjects with congenital AT-III deficiency.
Phase:
Phase 2/Phase 3
Details
Lead Sponsor:
Grifols Biologicals Inc.
Grifols Biologicals, LLC
Treatments:
Antithrombin III
Antithrombins