Small molecule (PROTAC degrader) · Degrader of Bruton's tyrosine kinase (BTK) · developed by Ascentage Pharma Group
APG-3288 is an orally bioavailable PROTAC that targets and degrades Bruton's tyrosine kinase (BTK) by recruiting cereblon to form a ternary complex, leading to proteasome-mediated BTK degradation. It blocks BTK/B-cell antigen receptor signaling and inhibits growth of malignant B-cells. It is studied in relapsed/refractory B-cell lymphomas and chronic lymphocytic leukemia.
Summary written with AI from the sources listed at the end of this page.
| Trial | Phase | Condition | Status | Sponsor |
|---|---|---|---|---|
| NCT07424833 | Phase 1 | Relapsed/Refractory Hematological Malignancies | Recruiting | AAPG |
Trials of the companies BioRadar tracks, from ClinicalTrials.gov, most advanced phase first.
Relapsed/Refractory Follicular Lymphoma (FL)Relapsed/Refractory Hematological MalignanciesRelapsed/Refractory Mantle Cell Lymphoma (MCL)Relapsed/Refractory Marginal Zone Lymphoma (MZL)Relapsed/Refractory Waldenström Macroglobulinemia (WM)
Updated Oct 3, 2026. Something wrong or missing? Report it on the AAPG page.
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