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NCT06561425 | RECRUITING | Relapsed/Refractory B-cell Non-Hodgkin Lymphoma

A Study Evaluating the Safety and Efficacy of GLPG5101 (19CP02) in Participants With Non-Hodgkin Lymphoma
Sponsor:

Galapagos NV

Brief Summary:

This study is evaluating whether an experimental treatment called GLPG5101 helps to treat non-Hodgkin lymphoma (NHL) and if it is safe to use. This study will be carried out in 2 phases: * The first phase is to see which doses of GLPG5101 work best with the least number of side effects. * In the second phase, participants will receive the selected dose(s) based on the results in the first phase.

Condition or disease

Relapsed/Refractory B-cell Non-Hodgkin Lymphoma

Lymphomas Non-Hodgkin's B-Cell

Intervention/treatment

GLPG5101

Phase

PHASE1

PHASE2

Detailed Description:

Phase 1 Dose escalation phase: The dose escalation phase is designed to select the doses for dose expansion based on efficacy and safety outcomes. Three dose levels of GLPG5101 will be evaluated to determine the recommended phase 2 doses (RP2Ds). Participants with aggressive or indolent forms of Relapsed/Refractory B-cell Non-Hodgkin Lymphoma (r/r NHL) including follicular lymphoma (FL), marginal zone lymphoma (MZL), mantle cell lymphoma (MCL), and Diffuse large B-cell lymphoma (DLBCL) will be enrolled. In case any safety or efficacy differences based on histological subtype of the disease are observed, it may be decided to make decisions regarding dose escalation for a specific subtype(s) independently, upon recommendation by the Safety Review Committee (SRC). Hence the RP2Ds may be different for different subtypes. Phase 2 Dose expansion phase: After determination of the RP2Ds, the study continues with the dose expansion phase. Different doses deemed safe by the SRC within the same indication may be explored in the dose-expansion phase to help select the optimal dose for further development. During this phase, participants will be enrolled into separate disease cohorts as defined by their NHL subtype: * Cohort 1a: DLBCL second line or greater (2L+) * Cohort 1b: DLBCL 2L+ with secondary central nervous system lymphoma (SCNSL) * Cohort 2: High-risk first-line DLBCL * Cohort 3: Indolent B-cell NHL (FL and MZL third-line or greater \[3L+\]) * Cohort 4: MCL 2L+ * Cohort 5: BL 2L+ * Cohort 6a: PCNSL 2L+ * Cohort 6b: PCNSL first-line consolidation * Cohort 7: DLBCL-RT 2L+ Participants per disease cohort will be treated at the selected RP2Ds for that disease subtype.

Study Type : INTERVENTIONAL
Estimated Enrollment : 250 participants
Masking : NONE
Primary Purpose : TREATMENT
Official Title : A Phase I/II, Multicenter Study Evaluating the Feasibility, Safety, and Efficacy of Point-of-care Manufactured GLPG5101 (19CP02) in Subjects With Relapsed/Refractory B-cell Non-Hodgkin Lymphoma
Actual Study Start Date : 2022-03-09
Estimated Primary Completion Date : 2029-07-01
Estimated Study Completion Date : 2029-07-01

Information not available for Arms and Intervention/treatment

Ages Eligible for Study: 18 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers:
Criteria
Key Inclusion Criteria
  • * Histologically confirmed diagnosis of one of the following NHL subtypes: DLBCL, FL grade 1, 2 or 3A, MZL, MCL, BL, PCNSL, DLBCL-RT, High Grade B-cell Lymphoma (HGBL)
  • * Relapsed or refractory disease
  • * Presence of at least one measurable lesion according to the Lugano classification (except for PCNSL subjects ineligible for ASCT after induction therapy, Cohort 6b)
  • * Eastern Cooperative Oncology Group (ECOG) performance status of 0-2 (Participants with ECOG 2 must have serum albumin ≥ 3.4 gram/deciliter)
  • * Adequate bone marrow function
  • * Adequate renal, hepatic and pulmonary function
  • * Women of childbearing potential must have a negative serum pregnancy test at screening and prior to the first dose of conditioning chemotherapy
  • * Women of childbearing potential and all male subjects must agree to use highly effective methods of contraception and agree to remain on a highly effective method of contraception from the time of signing the informed consent form until at least 12 months after GLPG5101 infusion. Subjects must agree to not donate eggs or sperm during this period.
  • Key Exclusion Criteria
    • * Selected prior treatments as defined in the protocol
    • * History of another primary malignancy that requires intervention beyond surveillance or that has not been in remission for at least 3 years. (exceptions per protocol)
    • * Toxicity from previous anticancer therapy that has not resolved to baseline levels or to ≤ Grade 2
    • * Active central nervous system (CNS) involvement (lesion on contrast-enhanced CT/MRI brain, malignant B cells in CSF) by disease under study (exceptions per protocol)
    • * Clinically significant cardiac disease
    • * Primary immunodeficiency
    • * Stroke or seizure within 6 months of screening
    • * History of autoimmune disease requiring systemic immunosuppression or disease modifying treatment within 28 days before screening
    • * Infection with human immunodeficiency virus (HIV), active hepatitis B or active hepatitis C virus
    • * Systemic fungal, bacterial, viral, or other infection that is not controlled
A Study Evaluating the Safety and Efficacy of GLPG5101 (19CP02) in Participants With Non-Hodgkin Lymphoma

Location Details

NCT06561425

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How to Participate

Want to participate in this study, select a site at your convenience, send yourself email to get contact details and prescreening steps.

Locations

RECRUITING

United States, Massachusetts

Tufts Medical Center

Boston, Massachusetts, United States, 02111

RECRUITING

United States, Massachusetts

Beth Israel Deaconess Medical Center

Boston, Massachusetts, United States, 02215

RECRUITING

Belgium,

Antwerp University Hospital

Edegem, Belgium, 2650

RECRUITING

Belgium,

UZ Leuven

Leuven, Belgium, 3000

RECRUITING

Belgium,

CHU De Liège

Liège, Belgium, 4000

RECRUITING

Belgium,

Saint-Luc university clinics

Woluwe-Saint-Lambert, Belgium, 1200

RECRUITING

Netherlands,

Academic Medical Center

Amsterdam, Netherlands, 1105 is

RECRUITING

Netherlands,

Leiden University Medical Center

Leiden, Netherlands, 2333 for

RECRUITING

Netherlands,

Erasmus University Medical Center Rotterdam (Erasmus MC)

Rotterdam, Netherlands, 3015 GD