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

현재 선택: 1 · 임상 갱신 필요 1

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API CSV30행 · 1개 프로그램

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항목
ADCStandard DatabasestalePhase 2
PV (Polatuzumab vedotin, Polatuzumab vedotin (PV))
Roche / Genentech·Diffuse Large B-cell Lymphoma
177 trials·t½ 12.2 h
Overview
Program
Polatuzumab vedotin (PV)
Overview
Company
Roche / Genentech
Overview
Modality
ADC
Overview
Target
Diffuse Large B-cell Lymphoma
Overview
Indication
Diffuse Large B-cell Lymphoma
Overview
Phase
PHASE_2
Overview
Status
DISCONTINUED
Overview
Content status
Standard Database
Overview
Data Confidence
Data Confidence · Medium
Overview
Development Signal
Development Signal · Emerging
Overview
Approval status
Investigational
Technology
Payload
vedotin plus rituximab, cyclophosphamide, doxor
Technology
Linker
linker
MoA
Mechanism
targeting EGFR and CDK receptor
MoA
Biomarker
biomarkers remaining within normal ranges
PK/PD
Half-life
12.2 h
PK/PD
Species
Mouse, 24 mg/L
PK/PD
Animal (cat.)
Mouse, In vitro
PK/PD
Experiment
PK
Toxicology
Species
Mouse, 24 mg/L
Toxicology
Animal (cat.)
Mouse, In vitro
Toxicology
Major finding
Heterocycle-Substituted α-Methylene-γ-Butyrolactone Derivatives: Design, Synthesis, and Bioactivity against Phytopathogenic Fungi and Bacteria.. A series of 37 heterocycle-substituted α-methylene-γ-butyrolactone (MBL) derivatives were designed and synthesized. Bioassays showed that these derivatives possessed prominent fungicidal and bactericidal activities against Phytopht…
Toxicology
CRS
Reported
Clinical
Safety signal
Heterocycle-Substituted α-Methylene-γ-Butyrolactone Derivatives: Design, Synthesis, and Bioactivity against Phytopathogenic Fungi and Bacteria.. A series of 37 heterocycle-substituted α-methylene-γ-butyrolactone (MBL) derivatives were designed and synthesized. Bioassays showed that these derivatives possessed prominent fungicidal and bactericidal activities against Phytopht…
Clinical
Selected reported efficacy
ORR 100%
Clinical
Reported ORR
100.0%
Clinical
Result source
ClinicalTrials.gov NCT02611323
Clinical
Program phase
PHASE_2
Clinical
Trial activity
No active/completed counts
Clinical
Trial ref
NCT02611323