A Database Survey to Evaluate the Safety of Immune Globulin Subcutaneous (Human), 20% Solution in Participants With Primary Immunodeficiency

Recruiting Observational Study
Primary Immunodeficiency Diseases (PID)
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Sex
Any
Study type
Observational
Participants needed
100 (estimated)
Sponsor
Takeda · Industry
Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial

This study is a retrospective database study in Japan to evaluate the safety of Immune Globulin Subcutaneous (Human), 20% Solution in participants with primary immunodeficiency disease (PID). This survey will conduct in use of medical database called PIDJ2.

Trial Locations
Loading…

Loading trial locations…

Eligibility Criteria
Inclusion Criteria: 1. Patients with primary immunodeficiency (PID) enrolled in the PID patient registry. 2. Participant for whom study drug is entered in the therapeutic drug field on the data set. 3. Participant who is entered the intractable disease diagnosis corresponding to PID in the intracta…
Contacts

Takeda Contact

+1-877-825-3327

medinfoUS@takeda.com

CONTACT

Study Director

CONTACT