Small molecule · Inhibitor of Bruton's tyrosine kinase (BTK) · developed by Loxo Oncol
Pirtobrutinib is a small molecule, noncovalent inhibitor of Bruton's tyrosine kinase (BTK), binding both wild type BTK and BTK with C481 mutations. It blocks BTK signaling in the B-cell antigen receptor and cytokine receptor pathways that drive malignant B-cell proliferation. It is used in mantle cell lymphoma and chronic lymphocytic leukemia or small lymphocytic lymphoma.
Summary written with AI from the sources listed at the end of this page.
From the indications section of the FDA label (version of Mar 6, 2026). Read the full label for the exact wording, limitations and safety information.
| Trial | Phase | Condition | Status | Sponsor |
|---|---|---|---|---|
| NCT06721013 | Phase 1/2 | Immune Thrombocytopenia (ITP) | Recruiting | LLY |
Trials of the companies BioRadar tracks, from ClinicalTrials.gov, most advanced phase first.
Immune Thrombocytopenia (ITP)
Updated Oct 11, 2026. Something wrong or missing? Report it on the LLY page.
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