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항목
CGTStandard DatabasestalePhase 1
chimeric antigen receptor T cell treatment (chimeric antigen receptor T cell treatment)
Yake Biotechnology Ltd.·FRα
62 trials
Overview
Program
chimeric antigen receptor T cell treatment
Overview
Company
Yake Biotechnology Ltd.
Overview
Modality
CGT
Overview
Target
FRα
Overview
Indication
T Cell Lymphoma; T-cell Leukemia
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
lentiviral transfection
MoA
Mechanism
Targeted immunotherapies like chimeric antigen receptor
MoA
Biomarker
CD19-targeting CAR-T cells were successfully constructed, and the positive
PK/PD
Species
Mouse, Human
PK/PD
Animal (cat.)
Human, Mouse, In vitro
PK/PD
Experiment
PD
Toxicology
Species
Mouse, Human
Toxicology
Animal (cat.)
Human, Mouse, In vitro
Toxicology
Major finding
Management of chimeric antigen receptor T-cell-related toxicity of a patient affected by cytokine release syndrome and immune effector cell-associated neurotoxicity syndrome, followed by an intestinal perforation: a case report.. Mantle cell lymphoma is a diverse B-cell lymphoma with varying clinical behaviors. Treating relapsed or refractory mantle cell lymphoma is challenging, with Bruton's tyro…
Toxicology
CRS
Reported
Clinical
Safety signal
Management of chimeric antigen receptor T-cell-related toxicity of a patient affected by cytokine release syndrome and immune effector cell-associated neurotoxicity syndrome, followed by an intestinal perforation: a case report.. Mantle cell lymphoma is a diverse B-cell lymphoma with varying clinical behaviors. Treating relapsed or refractory mantle cell lymphoma is challenging, with Bruton's tyro…
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