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7UY",{"type":52,"coordinates":1855},[1856,1857],1.29834,52.62783,{"lat":1857,"lon":1856},{"facility":1860,"status":45,"city":1861,"state":26,"zip":1862,"country":1834,"countryCode":1835,"cosmosGeoPoint":1863,"geoPoint":1867,"contacts":26},"Spire Leeds Healthcare Spire Leeds Hospital","Roundhay","LS8 1NT",{"type":52,"coordinates":1864},[1865,1866],-1.5074,53.83052,{"lat":1866,"lon":1865},{"facility":1869,"status":45,"city":1870,"state":26,"zip":1871,"country":1834,"countryCode":1835,"cosmosGeoPoint":1872,"geoPoint":1876,"contacts":26},"Salisbury Foundation Trust","Salisbury","SP2 8BJ",{"type":52,"coordinates":1873},[1874,1875],-1.79569,51.06931,{"lat":1875,"lon":1874},{"type":1878,"investigatorFullName":26,"investigatorTitle":26,"investigatorAffiliation":26,"oldNameTitle":26,"oldOrganization":26},"SPONSOR","100590881","phase-3-a-study-to-evaluate-the-safety-and-efficacy-of-bgb-16673-compared-to-pirtobrutinib-in-adults-with-relapsedrefractory-chronic-lymphocytic-leukemia-or-small-lymphocytic-lymphoma-100590881",false,"NCT06973187","A Study to Evaluate the Safety and Efficacy of BGB-16673 Compared to Pirtobrutinib in Adults With Relapsed\u002FRefractory Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma","A Phase 3, Open-Label, Randomized Study to Evaluate the Safety and Efficacy of BGB-16673 Compared to Pirtobrutinib in Patients With Relapsed\u002FRefractory Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma","Inclusion Criteria:\n\n* Confirmed diagnosis of CLL or SLL, requiring treatment, based on 2018 iwCLL criteria\n* Previously received treatment for CLL\u002FSLL with a covalent Bruton tyrosine kinase inhibitor (cBTKi). Patients should have disease relapsed after or refractory to at least 1 line of therapy including a cBTKi.\n* Participants with SLL must have measurable disease by computed tomography\u002Fmagnetic resonance imaging, defined as ≥ 1 lymph node \\> 1.5 cm in longest diameter and measurable in 2 perpendicular diameters.\n\nExclusion Criteria:\n\n* Known prolymphocytic leukemia or history of, or currently suspected, Richter's transformation.\n* History of known bleeding disorder such as hemophilia A, hemophilia B, von Willebrand disease, or history of spontaneous bleeding requiring blood transfusion or other medical intervention\n* History of ischemic stroke or intracranial hemorrhage within 6 months before first dose of study drug\n* Prior exposure to any Bruton tyrosine kinase (BTK) protein degraders or noncovalent Bruton tyrosine kinase inhibitor (ncBTKi).\n* Current or history of central nervous system involvement including the brain, spinal cord, leptomeninges, and cerebrospinal fluid (as documented by imaging, cytology, or biopsy) by CLL\u002FSLL\n\nNOTE: Other protocol defined Inclusion\u002FExclusion criteria may apply.","ALL","18 Years",{"count":1889,"type":1890},500,"ESTIMATED","INTERVENTIONAL",[1893],"PHASE3","The purpose of this study is to evaluate the efficacy and safety of BGB-16673 alone compared with pirtobrutinib in patients with relapsed or refractory (R\u002FR) chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) who had been previously treated with a covalent Bruton tyrosine kinase inhibitor (cBTKi).",[1896,1897],"Chronic Lymphocytic Leukemia","Small Lymphocytic Lymphoma",[1899,1900],"Noncovalent Bruton tyrosine kinase inhibitor","Bruton tyrosine kinase-targeted protein degrader","2026-08-05",{"date":1903,"type":1904},"2026-08-06","ACTUAL",{"date":1906,"type":1904},"2025-09-04",{"date":1908,"type":1890},"2028-04-17",{"name":5,"class":6},204]