Primary Immunodeficiency Diseases (PID)

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Review clinical trials related to Primary Immunodeficiency Diseases (PID). Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

A Study of TAK-664 in People With Primary Immunodeficiency Diseases Who Have Not Yet Been Treated With Immunoglobulins

Primary immunodeficiency disease (or PIDD) is a group of conditions in which the immune system does not work properly. Some people with PIDD do not make enough antibodies. Antibodies are proteins that help to either protect the body from infections or fight infections. The main type of antibodies that helps protect the body from infection is IgG. People who do not make enough IgG often need medical treatment that gives the body those antibodies. This treatment is called IgG replacement therapy. It can be given through a vein (intravenous or IV) or under the skin (subcutaneous SC). TAK-664 is approved worldwide for SC IG replacement therapy. The study wants to learn more about TAK-664 given to people with PIDD who have not yet been treated with IG (called 'treatment-naïve'). The main aim of the study is to check if giving TAK-664 daily for 5 days, and then once more 3 days later (Day 8), can raise IgG to the target level and keep IgG there. Another aim of the study is to learn if TAK-664 given once a week can keep the IgG at the target levels during the study. The study also wants to find out how much the IgG levels raise and learn how many infections occur and how they are treated.

Participants needed: 9
Trial details
Phase: Phase 4Age: 6+Biological sex: AllType: InterventionalSponsor: TakedaUpdated: Sep 8, 2026
Eligibility criteria

The participant or the participant's legally authorized representative is willin... [+6]

The participant has significant proteinuria (greater than or equal to [>=] 3 and... [+22]

Status: Recruiting

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

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.

Participants needed: 100
Trial details
Biological sex: AllType: ObservationalSponsor: TakedaUpdated: Aug 7, 2026Locations: 1
Eligibility criteria

Patients with primary immunodeficiency (PID) enrolled in the PID patient registr... [+3]

Participant for whom study drug has not been entered in the drug name in the med... [+2]

Status: Recruiting

Ex Vivo Evaluation of JAK-inhibitor and Gene Therapeutical Approach in JAK-STAT Related Disorders

The investigators want to study the JAK-inhibitors and their impact on the immune system and evaluate the potential of a gene-therapeutic strategy

Participants needed: 20
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: prof. dr. Rik SchrijversUpdated: Dec 3, 2025Locations: 1
Eligibility criteria

Cases (A): adult patients presenting with a genetically confirmed or highly susp... [+1]

Children (< 18 years at time of recruitment) [+1]

Status: Not yet recruiting

Efficacy, Safety and Pharmacokinetic of Virchow IVIG in PID Patients

The study duration for individual patients will be up to 55 weeks for the 4-weekly and 3- weekly schedule of the treatment which includes 3 weeks for screening, 48 weeks for Study Medication administration and 4 weeks for follow-up assessments

Participants needed: 44
Trial details
Phase: Phase 3Age: 2-65Biological sex: AllType: InterventionalSponsor: Virchow GroupUpdated: Jun 12, 2025Locations: 2
Eligibility criteria

Male or female, aged 2 to 65 years. [+11]

Pregnant women, nursing mothers or a planned pregnancy within 18 months of parti... [+15]

Status: Not yet recruiting

Inbon Errors of Immunity Attending Assiut University Children&Amp;#39;s Hospital: a Single Center Study

Aim of Study The aim of this study to describe the clinical profile of children diagnosed as IEIs who were admitted to in Assiut university children\&amp;#39;s Hospital.

Participants needed: 60
Trial details
Age: Up to 18Biological sex: AllType: ObservationalSponsor: Assiut UniversityUpdated: Oct 21, 2024
Eligibility criteria

patients without any criteria of ten warning signs