Bruton-type agammaglobulinemia
MONDO:0010421X-linked agammaglobulinemia (XLA) is a clinically variable form of isolated agammaglobulinemia, an inherited immunodeficiency disorder, and is characterized in affected males by recurrent bacterial infections during infancy.
Also known as: BTK-deficiency, Bruton type agammaglobulinemia, Bruton's Sex-linked agammaglobulinemia, Bruton's X-linked agammaglobulinemia, Bruton-type agammaglobulinemia, X-linked agammaglobulinemia, agammaglobulinemia, X-linked 1, X-linked recessive, Bruton's agammaglobulinemia
45 clinical trials for this condition and its sub-types, 4 tagged with Bruton-type agammaglobulinemia itself.
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Scientists launch major study to unravel mysteries of rare immune diseases
Knowledge-focused Recruiting nowThis study aims to understand the causes and progression of Common Variable Immunodeficiency (CVID) and related inborn errors of immunity. Researchers will observe up to 500 patients over time using blood tests, imaging, and other exams. The goal is to find better ways to diagnos…
Sponsor: National Institute of Allergy and Infectious Diseases (NIAID) • Aim: Knowledge-focused
Last updated Sep 03, 2026 00:00 UTC
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Scientists probe hidden IgE variants to unlock allergy mysteries
Knowledge-focused Recruiting nowThis study looks at different forms of IgE (a protein involved in allergic reactions) in healthy volunteers and people with conditions like severe allergies, chronic hives, mastocytosis, and immune deficiencies. Researchers aim to understand how these IgE variations relate to hea…
Sponsor: KU Leuven • Aim: Knowledge-focused
Last updated Jun 27, 2026 08:09 UTC