This study is currently not recruiting participants.

Randomized multicenter double-blind placebo-controlled parallel-group phase III study to investigate the efficacy safety and tolerability of 2 different doses of IgPro20 (subcutaneous immunoglobulin) for the treatment of chronic inflammatory demyelinating polyneuropathy (CIDP)

  • STATUS
    Not Recruiting
Updated on 19 February 2024

Summary

The purpose of this study is to show how effective two doses of IgPro20 are compared with placebo.

Description

The purpose of this study is to show how effective two doses of IgPro20 are compared with placebo.

Details
Condition Polyneuropathy
Age 18years - 100years
Clinical Study IdentifierTX3835
Last Modified on19 February 2024

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