A Phase 1/2, Open Label, Dose Ranging Study to Evaluate the Safety,Tolerability, Pharmacokinetics and Exploratory Efficacy Parameters of PRX-102 Administered by Intravenous Infusion Every 2 Weeks for 12 Weeks to Adult Fabry Patients

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Updated on 21 April 2022

Summary

A Phase 1/2, Open Label, Dose Ranging Study to Evaluate the Safety,Tolerability, Pharmacokinetics and Exploratory Efficacy Parameters of PRX-102 Administered by Intravenous Infusion Every 2 Weeks for 12 Weeks to Adult Fabry Patients

Description

To evaluate the safety and tolerability of a long-term enzyme replacement therapy(ERT) – PRX-102 – in adult subjects with Fabry disease.

Details
Condition Fabry Disease
Clinical Study IdentifierTX137404
Last Modified on21 April 2022

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