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타깃 · 모달리티 · 임상 근거 · 비임상 맥락으로 최대 5개 프로그램을 나란히 비교합니다. · 다음 갱신 D-6 · 마지막 9월 2일

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항목
CGTStandard DatabasestalePhase 2
CD19 CAR T cells (CD19 CAR T cells)
Bioceltech Therapeutics, Ltd.·CD19
128 trials
Overview
Program
CD19 CAR T cells
Overview
Company
Bioceltech Therapeutics, Ltd.
Overview
Modality
CGT
Overview
Target
CD19
Overview
Indication
Lymphomas Non-Hodgkin's B-Cell; Relapse
Overview
Phase
PHASE_2
Overview
Status
RECRUITING
Overview
Content status
Standard Database
Overview
Data Confidence
Data Confidence · Medium
Overview
Development Signal
Development Signal · Emerging
Overview
Approval status
Investigational
Technology
Vector
Lentiviral vectors (LVs) that facilitate gene delivery to desired cell types have been wid
MoA
Mechanism
CAR-T cells with increasing amounts of antigen-loaded beads yielded a dose-dependent secretion of IFN-γ, whereas non-loaded or MOCK antigen-loaded beads did n
MoA
Biomarker
CD19 CAR-T cells, cryopreserved CAR-T cells yielded low
PK/PD
Species
Mouse
PK/PD
Animal (cat.)
Mouse, In vitro
PK/PD
Experiment
PD
Toxicology
Species
Mouse
Toxicology
Animal (cat.)
Mouse, In vitro
Toxicology
Major finding
Pretreatment With BTK Inhibitors Improved the Sensitivity of DLBCL Cells to CAR-T Cells in a Coculture System by Downregulating the Polarisation of M2 Macrophages.. The tumour microenvironment (TME) of relapsed/refractory (R/R) diffuse large B-cell lymphoma (DLBCL) patients is associated with resistance of DLBCL cells to CD19 CAR-T cells. How to improve TME in DLBCL and improve the efficacy of CAR…
Toxicology
CRS
Reported
Clinical
Safety signal
Pretreatment With BTK Inhibitors Improved the Sensitivity of DLBCL Cells to CAR-T Cells in a Coculture System by Downregulating the Polarisation of M2 Macrophages.. The tumour microenvironment (TME) of relapsed/refractory (R/R) diffuse large B-cell lymphoma (DLBCL) patients is associated with resistance of DLBCL cells to CD19 CAR-T cells. How to improve TME in DLBCL and improve the efficacy of CAR…
Clinical
Selected reported efficacy
ORR 88%
Clinical
Reported ORR
88%
Clinical
Reported PFS
23.6
Clinical
Reported OS
NA
Clinical
Result source
ClinicalTrials.gov NCT04002401
Clinical
Program phase
PHASE_2
Clinical
Trial activity
No active/completed counts
Clinical
Trial ref
NCT04002401