RecruitingNCT06565078
A Database Survey to Evaluate the Safety of Immune Globulin Subcutaneous (Human), 20% Solution in Participants With Primary Immunodeficiency
Studying Primary immunodeficiency
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Takeda
- Intervention
- Immune Globulin Subcutaneous (Human), 20% Solution(drug)
- Enrollment
- 100 enrolled
- Eligibility
- All sexes
- Timeline
- 2025 – 2030
Study locations (1)
- Takeda selected site, Tokyo, Tokyo, Japan
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.
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