Phase 2 Study of Duvelisib in Previously Treated Patients With Chronic Lymphocytic Leukemia /Small Lymphocytic Lymphoma
Status: | Suspended |
---|---|
Conditions: | Blood Cancer, Lymphoma |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 12/13/2018 |
Start Date: | February 12, 2018 |
End Date: | March 2021 |
A Phase 2 Study of Duvelisib Efficacy and Safety in Patients With Chronic Lymphocytic Leukemia (CLL)/Small Lymphocytic Lymphoma (SLL) Previously Treated With a Bruton's Tyrosine Kinase Inhibitor (BTKi)
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 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.
bioavailable dual inhibitor of PI3K-δ,γ, in patients with 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.
Inclusion Criteria:
1. ≥ 18 years of age.
2. Diagnosis of CLL or SLL.
3. Received at least one prior anti-cancer therapy for CLL or SLL.
4. Previous exposure to BTKi and meet at least one of the criteria below:
1. Progressive disease (PD) while receiving or within 6 months after completing BTKi
therapy.
2. Discontinued a BTKi therapy due to BTKi treatment- related intolerance.
5. Measurable disease with a lymph node or tumor mass > 1.5 cm in at least one dimension.
6. Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2.
7. Resolution of toxicities due to prior BTKi therapy to acceptable level.
8. Willingness of male and female patients to use medically acceptable methods of birth
control.
9. Willing and able to participate in all required study evaluations and procedures.
Exclusion Criteria:
1. Richter's transformation or prolymphocytic leukemia
2. Uncontrolled autoimmune hemolytic anemia or thrombocytopenia
3. Received prior transplant
4. Experienced PD or serious adverse events on a prior phosphoinositide-3-kinase (PI3K)
inhibitor
5. Known central nervous system involvement by CLL/SLL
We found this trial at
8
sites
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Billings, Montana 59102
Principal Investigator: Patrick Cobb, MD
Phone: 406-238-6685
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Ingalls Memorial Hospital As the area's only independent not-for-profit healthcare system, Ingalls has the ability...
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La Jolla, California 92093
Principal Investigator: Thomas Kipps, MD
Phone: 858-246-0386
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Morristown, New Jersey 07960
Principal Investigator: Farber Charles, MD
Phone: 973-436-1755
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6001 North Mayfair Street
Spokane, Washington 99208
Spokane, Washington 99208
Principal Investigator: Arvind Chaudry, MD
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7695 South Research Drive
Tempe, Arizona 85206
Tempe, Arizona 85206
Principal Investigator: Kasra Karamlou, MD
Phone: 480-416-5079
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