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항목
ADCCurated CoreFDAApproved
telisotuzumab vedotin (Emrelis, ABBV-399, Teliso-V, telisotuzumab-vedotin-tllv)
AbbVie·c-Met
12 trials·t½ ADC in the range of days; free MMAE shorter
Overview
Program
Emrelis (telisotuzumab vedotin)
Overview
Company
AbbVie
Overview
Modality
ADC
Overview
Target
c-Met
Overview
Indication
Previously treated locally advanced or metastatic non-squamous NSCLC with high c-Met protein overexpression
Overview
Phase
APPROVED
Overview
Status
APPROVED
Overview
Content status
Curated Core
Overview
Data Confidence
Data Confidence · High
Overview
Development Signal
Development Signal · Established
Overview
Approval status
FDA approved
Positioning
Key differentiator
Selects high c-Met protein overexpression by IHC, not MET gene mutation. That split is the first row versus MET TKIs.
Positioning
Known limitation
c-Met down-regulation, MMAE efflux, and histologic transformation.
Positioning
Development positioning
Only approved c-Met ADC; confirmatory TeliMET NSCLC-01 versus docetaxel is ongoing.
Technology
Payload
MMAE (microtubule inhibitor)
Technology
Linker
Cleavable vc linker, vedotin chemistry
MoA
Mechanism
Anti-c-Met antibody binds and internalizes; the protease-cleavable linker releases MMAE, which disrupts microtubules and kills the cell plus neighbors via bystander diffusion.
MoA
Biomarker
VENTANA MET (SP44) companion diagnostic. High overexpression is ≥50% of cells with 3+ staining, not MET exon 14 skipping.
PK/PD
Half-life
ADC in the range of days; free MMAE shorter
PK/PD
Animal (cat.)
Human
Toxicology
Major finding
Peripheral neuropathy, fatigue, decreased appetite, and peripheral edema are common. Grade 3–4 lab signals include lymphopenia and transaminase rises.
Toxicology
CRS
N/A
Clinical
Safety signal
Peripheral neuropathy, fatigue, decreased appetite, and peripheral edema are common. Grade 3–4 lab signals include lymphopenia and transaminase rises.
Clinical
Selected reported efficacy
ORR 35%
Clinical
Reported ORR
35%
Clinical
Result source
LUMINOSITY (NCT03539536)
Clinical
Program phase
APPROVED
Clinical
Trial ref
NCT03539536