Chronic Lymphocytic Leukemia Clinical Trial
Phase 2 Study of Duvelisib in Previously Treated Patients With Chronic Lymphocytic Leukemia /Small Lymphocytic Lymphoma
Summary
This is a multi-center, single-arm, open-label, Phase 2 study of duvelisib, an orally bioavailable dual inhibitor of PI3K-δ,γ, in patients with leukemia-cll/" >CLL/SLL who have previously been treated with ibrutinib or another Bruton's Tyrosine Kinase Inhibitor (BTKi) and relapsed or were refractory to such therapy or discontinued such therapy due to toxicity.
Eligibility Criteria
Inclusion Criteria:
≥ 18 years of age.
Diagnosis of CLL or SLL.
Received at least one prior anti-cancer therapy for CLL or SLL.
Previous exposure to BTKi and meet at least one of the criteria below:
Progressive disease (PD) while receiving or within 6 months after completing BTKi therapy.
Discontinued a BTKi therapy due to BTKi treatment- related intolerance.
Measurable disease with a lymph node or tumor mass > 1.5 cm in at least one dimension.
Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2.
Resolution of toxicities due to prior BTKi therapy to acceptable level.
Willingness of male and female patients to use medically acceptable methods of birth control.
Willing and able to participate in all required study evaluations and procedures.
Exclusion Criteria:
Richter's transformation or prolymphocytic leukemia
Uncontrolled autoimmune hemolytic anemia or thrombocytopenia
Received prior transplant
Experienced PD or serious adverse events on a prior phosphoinositide-3-kinase (PI3K) inhibitor
Known central nervous system involvement by CLL/SLL
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There are 8 Locations for this study
Tempe Arizona, 85284, United States
Hot Springs Arkansas, 71913, United States
La Jolla California, 92093, United States
Harvey Illinois, 60426, United States
Royal Oak Michigan, 48073, United States
Billings Montana, 59102, United States
Morristown New Jersey, 07932, United States
Spokane Washington, 99208, United States
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