Clinical trial · Interventional
Safety and Efficacy of BKM120 in Relapsed and Refractory NHL
An Open-label Phase II Study of BKM120 in Subjects With Relapsed and Refractory Diffuse Large B-cell Lymphoma, Mantle Cell Lymphoma and Follicular Lymphoma
NCT01693614CI-TRIAL-00035083completedPhase 2Results postedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This is a phase II study evaluating the safety, tolerability and efficacy of BKM120 in patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL), mantle cell lymphoma (MCL) or follicular lymphoma (FL).
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Diffuse Large B-cell Lymphoma, Mantle Cell Lymphoma, Follicular Lymphoma | Diffuse Large B-Cell Lymphoma | CURATED_BROADER | 0.80 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Buparlisib | Drug | Buparlisib | ALIAS |
Design
Arms and outcomes
Arms (3)
- type
- EXPERIMENTAL
- label
- DLBCL Cohort
- description
- Diffuse large B-cell lymphoma cohort
- interventionNames
- Drug: Buparlisib
- type
- EXPERIMENTAL
- label
- MCL Cohort
- description
- Mantle cell lymphoma cohort
- interventionNames
- Drug: Buparlisib
- type
- EXPERIMENTAL
- label
- FL Cohort
- description
- Follicular lymphoma cohort
- interventionNames
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Patient had a histologically confirmed diagnosis of mantle cell lymphoma, follicular lymphoma, or diffuse large B cell lymphoma. 2. Patient had relapsed or refractory disease and received at least one prior therapy. 3. Patient with diffuse large B cell lymphoma had received or was ineligible for autologous or allogeneic stem cell transplant. 4. Patient had at least one measurable nodal lesion (≥2 cm) according to Cheson criteria (Cheson 2007). In case where the patient had no measurable nodal lesions ≥ 2 cm in the long axis at baseline, then the patient must have had at least one measurable extra-nodal lesion. 5. Patient had an Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2. 6. Patient had adequate bone marrow and organ function. Exclusion Criteria: 1. Patient had received previous treatment with PI3K inhibitors 2. Patient had evidence of graft versus host disease (GVHD). 3. Patient had active or history of central nervous system (CNS) disease. 4. Patient had a concurrent malignancy or had a malignancy within 3 years of study enrollment (with the exception of adequately treated basal or squamous cell carcinoma or non-melanomatous skin cancer). 5. Patient had a score ≥ 12 on the PHQ-9 questionnaire. 6. Patient had a GAD-7 mood scale score ≥ 15. 7. Pregnant or nursing women 8. Patient who did not use highly effective contraception methods to avoid becoming pregnant or conceiving offspring.
References
Publications (1)
- DERIVEDYounes A, Salles G, Martinelli G, Bociek RG, Barrigon DC, Barca EG, Turgut M, Gerecitano J, Kong O, Pisal CB, Tavorath R, Kim WS. Pan-phosphatidylinositol 3-kinase inhibition with buparlisib in patients with relapsed or refractory non-Hodgkin lymphoma. Haematologica. 2017 Dec;102(12):2104-2112. doi: 10.3324/haematol.2017.169656. Epub 2017 Sep 29. PMID 28971900