Last updated on September 2018

Long-Term Tolerability and Safety of HYQVIA/HyQvia in CIDP

Brief description of study

The purpose of this study is to assess the long-term safety, tolerability, and immunogenicity of the subcutaneous (SC) treatment with Immune Globulin Subcutaneous (IGSC) facilitated with recombinant human hyaluronidase (rHuPH20) (HYQVIA/HyQvia) in participants with chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) who have completed Baxalta Clinical Study Protocol 161403 Epoch 1 or Clinical Study Protocol 161601 without CIDP worsening.

Clinical Study Identifier: NCT02955355

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Clinical Center Nis

Nis, Serbia
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Recruitment Status: Open

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