At a glance
ClinicalIndex Comparison RecordPhase 2Completed· 159 enrolled
Drug / intervention
Axicabtagene ciloleucel +2 morebiological
Likely dose
Axicabtagene ciloleucel administered intravenously (specific dose not stated in protocol)AI-extracted
Key inclusion· 4
- ✓Follicular lymphoma or marginal zone lymphoma with disease progression after at least 2 prior lines of combination chemoimmunotherapy
- ✓Measurable disease present
- ✓No known CNS involvement by lymphoma
- ✓ECOG performance status 0-1 with adequate renal, hepatic, pulmonary, and cardiac function
Key exclusion· 5
- ✕Transformed follicular or marginal zone lymphoma
- ✕Small lymphocytic lymphoma
- ✕Histological Grade 3b follicular lymphoma
- ✕Autologous transplant within 6 weeks of leukapheresis or any prior allogeneic transplant
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Phase 2 Multicenter Study of Axicabtagene Ciloleucel in Subjects With Relapsed/Refractory Indolent Non-Hodgkin Lymphoma (iNHL)
In Brief
A Phase 2 clinical trial evaluating Axicabtagene ciloleucel, Cyclophosphamide, and 1 other intervention for Follicular Lymphoma and 2 related conditions. Completed, enrolled 159 participants across 19 sites in 2 countries.
Detailed Summary
The goal of this study is to assess whether axicabtagene ciloleucel improves the clinical outcome in participants with relapsed or refractory indolent non-Hodgkin lymphoma (r/r) iNHL.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesFrance, United States
Collaborators--
Timeline
Phase 2CompletedFinished
201820192020202120222023202420252026
First PostedApr 2017
Enrollment StartJun 2017
Primary CompletionDec 2024
TodayJul 2026
First PostedApr 7, 2017
Enrollment StartJun 6, 2017
Primary CompletionDec 20, 2024
TodayJul 2, 2026
Enrollment to primary: 7.5 yearsPosted 9.2 years ago
Interventions
Axicabtagene ciloleucelbiological
Administered intravenously
Cyclophosphamidedrug
Administered intravenously
Fludarabinedrug
Administered intravenously