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항목
CGTStandard DatabasestalePhase 1
CD4 CAR T cells (CD4 CAR T cells)
iCell Gene Therapeutics·FRα
39 trials
Overview
Program
CD4 CAR T cells
Overview
Company
iCell Gene Therapeutics
Overview
Modality
CGT
Overview
Target
FRα
Overview
Indication
T Cell Lymphoma in Relapse; Refractory T-Cell Lymphoma
Overview
Phase
PHASE_1
Overview
Status
ACTIVE
Overview
Content status
Standard Database
Overview
Data Confidence
Data Confidence · Medium
Overview
Development Signal
Development Signal · Watch
Overview
Approval status
Investigational
Technology
Vector
retroviral therapy (ART)
MoA
Mechanism
targetable modulator of JAK-STAT signaling
MoA
Biomarker
biomarker and therapeutic target in CAR T cell-associated neurotoxicity
PK/PD
Species
Mouse
PK/PD
Animal (cat.)
Mouse, In vitro
PK/PD
Experiment
The CXCL16/CXCR6 axis is linked to immune effector cell-associated neurotoxicity in chimeric antigen receptor (CAR) T cell therapy.
Toxicology
Species
Mouse
Toxicology
Animal (cat.)
Mouse, In vitro
Toxicology
Major finding
Multiomic and Longitudinal Dissection of Immune Dynamics Associated with Parkinsonism after Ciltacabtagene Autoleucel Therapy.. We report a fatal case of parkinsonism following treatment with ciltacabtagene autoleucel (cilta-cel). To investigate underlying mechanisms, we performed a multipronged longitudinal analysis using single-cell RNA (scRNA)/T-cell receptor (TCR) sequencing, flow cytometry, a…
Toxicology
CRS
Reported
Clinical
Safety signal
Multiomic and Longitudinal Dissection of Immune Dynamics Associated with Parkinsonism after Ciltacabtagene Autoleucel Therapy.. We report a fatal case of parkinsonism following treatment with ciltacabtagene autoleucel (cilta-cel). To investigate underlying mechanisms, we performed a multipronged longitudinal analysis using single-cell RNA (scRNA)/T-cell receptor (TCR) sequencing, flow cytometry, a…
Clinical
Selected reported efficacy
ORR 80.3%
Clinical
Reported ORR
80.3%
Clinical
Reported PFS
9.03
Clinical
Reported OS
NA
Clinical
Result source
ClinicalTrials.gov NCT03483103
Clinical
Program phase
PHASE_1
Clinical
Trial ref
NCT03483103