Chronic Lymphocytic Leukemia Clinical Trial

Study of Autologous Peripheral Blood Lymphocytes in the Treatment of Patients With CLL or SLL

Summary

This is a Phase 1/2, study evaluating IOV-2001 (Adoptive Cell Therapy) composed of autologous PBL (Peripheral Blood Lymphocytes) in patients with leukemia-cll/" >CLL/SLL, which has relapsed or is relapsing during treatment with ibrutinib or acalabrutinib.

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Full Description

This study involves patients receiving nonmyeloablative (NMA) lymphocyte depleting (LD) preparative regimen prior to infusion of IOV-2001 followed by IL-2 administration.

In Phase 1, patients meeting the eligibility criteria will be enrolled and will receive treatment with IOV-2001 followed by low dose IL-2 or high dose IL-2.

After completion of Phase 1, the recommended Phase 2 dose (RP2D) will be evaluated in selected patient cohorts defined in the Phase 2 part of the study.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Patients with CLL or SLL with radiographically measurable disease

Cohort 2 only: patients with progressed or progressing CLL/SLL on ibrutinib or acalabrutinib with del 17p and/or TP53 mutated
Cohort 3 only: patients with progressed or progressing CLL/SLL on ibrutinib or acalabrutinib without del 17p and/or TP53 mutated
Patients must have documented progression or be progressing on ibrutinib or acalabrutinib, as indicated by the presence of known BTK resistance mutation

Patients must have received at least 1 prior regimen (only for patients without del 17p and/or TP53 mutated) and currently be on ibrutinib or acalabrutinib. For patients on combination therapy as the last line of therapy prior study entry, progression to any of the individual components of the combination therapy, rather than to the combination regimen, is required.

For Cohort 2: The single prior regimen can be ibrutinib or acalabrutinib (ie, patients are eligible while progressing on their first line of therapy)
For Cohort 3: Patients must have progressed on at least 1 additional line of therapy in addition to ibrutinib or acalabrutinib
Patients must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 and an estimated life expectancy of ≥ 3 months.
Patients must have adequate bone marrow function to receive NMA-LD
Pulmonary function assessed by spirometry demonstrating FEV1 > 50% predicted normal
Cardiac function demonstrating left ventricular ejection fraction (LVEF) > 45%
Patients of childbearing potential or their partners of childbearing potential must be willing to practice an approved method of birth control during treatment and for 12 months after receiving the last protocol-related therapy.

Exclusion Criteria:

Patients who have received an organ allograft or prior cell transfer therapy within 20 years.
Patients with known or suspected transformed disease (ie, Richter's Transformation).
Patients who received treatment with any systemic chemotherapy, immunotherapy, targeted small molecule inhibitors, or other biologic agents within 30 days or 5 half-lives, whichever is shorter, of IOV-2001 infusion with the exception of ibrutinib or acalabrutinib
Patients with known involvement of central nervous system (CNS) by lymphoma or leukemia
Patients who are on chronic systemic steroid therapy >5 mg/day prednisone equivalent for any reason
Patients who have active systemic infections requiring systemic ABX, autoimmune anemia or thrombocytopenia, coagulation disorders, or other active major medical illnesses of the cardiovascular, respiratory, or immune system.

Patients who are seropositive for any of the following:

Human immunodeficiency virus (HIV)-1 or HIV-2 antibodies
Hepatitis B antigen (HbsAg) or anti-hepatitis B core total antibodies (anti-HbcAb), or hepatitis C antibody (HCVAb)
Patients with active and chronic fungal, bacterial, or viral infection requiring IV treatment
Patients who require treatment for anti-coagulation with a vitamin K antagonist (warfarin)
Patients who have received a live or attenuated vaccine within 28 days of beginning the preparative NMA-LD regimen
Patients who are pregnant or breastfeeding

Study is for people with:

Chronic Lymphocytic Leukemia

Phase:

Phase 1

Estimated Enrollment:

70

Study ID:

NCT04155710

Recruitment Status:

Active, not recruiting

Sponsor:

Iovance Biotherapeutics, Inc.

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There are 4 Locations for this study

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Moffitt Cancer Center
Tampa Florida, 33612, United States
University of Cincinnati Medical Center
Cincinnati Ohio, 45219, United States
Ohio State University
Columbus Ohio, 43210, United States
Allegheny Health
Pittsburgh Pennsylvania, 15224, United States

How clear is this clinincal trial information?

Study is for people with:

Chronic Lymphocytic Leukemia

Phase:

Phase 1

Estimated Enrollment:

70

Study ID:

NCT04155710

Recruitment Status:

Active, not recruiting

Sponsor:


Iovance Biotherapeutics, Inc.

How clear is this clinincal trial information?

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