UnknownPhase 3NCT06089122

Efficacy, Safety, and Pharmacokinetics of Shu Yang IVIG

Studying Primary immunodeficiency

Last synced from ClinicalTrials.gov May 1, 2026

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Key facts

Sponsor: Azidus Brasil
Principal Investigator: Luciana Ferrara, RNP
Azidus Brasil
Intervention: IVIG(biological)
Enrollment: 50 enrolled
Eligibility: 6-60 years · All sexes
Timeline: 2024 – 2025

Collaborators

Sichuan Yuanda Shuyang Pharmaceutical Co., Ltd.

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT06089122 on ClinicalTrials.gov

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