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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

프로그램 상세에서 관심 등록 후 2개 이상 모으면 여기서 한 번에 비교할 수 있습니다.

API CSV29행 · 1개 프로그램

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항목
AntibodyLimited DatastalePhase 3
Anti-PD-1 monoclonal antibody (Anti-PD-1 monoclonal antibody)
Shanghai Celfuture Biotech Co., Lt…·PD-1
136 trials·t½ 13 h
Overview
Program
Anti-PD-1 monoclonal antibody
Overview
Company
Shanghai Celfuture Biotech Co., Ltd.
Overview
Modality
ANTIBODY
Overview
Target
PD-1
Overview
Indication
Colorectal Cancer
Overview
Phase
PHASE_3
Overview
Status
RECRUITING
Overview
Content status
Limited Data
Overview
Data Confidence
Data Confidence · Low
Overview
Development Signal
Development Signal · Emerging
Overview
Approval status
Investigational
MoA
Mechanism
checkpoint inhibitor-induced 3M syndrome: a case report
MoA
Biomarker
PD-1 treatment in shaping tumor-regional CD39 + CD8 + T cells high
PK/PD
Half-life
13 h
PK/PD
Species
Mouse
PK/PD
Animal (cat.)
Mouse
PK/PD
Experiment
PD
Toxicology
Species
Mouse
Toxicology
Animal (cat.)
Mouse
Toxicology
Major finding
Sequential involvement of hypoxia and anti-PD-1 treatment in shaping tumor-regional CD39 + CD8 + T cells highlights immunotherapy-resistant features in NSCLC.. Understanding resistance to anti-programmed cell death protein 1 (PD-1) therapy is critical for developing reversal strategies. Although ectonucleotidase CD39 (ENTPD1) (CD39) + cluster of differentiation 8 (CD8) + T cells have been associat…
Clinical
Safety signal
Sequential involvement of hypoxia and anti-PD-1 treatment in shaping tumor-regional CD39 + CD8 + T cells highlights immunotherapy-resistant features in NSCLC.. Understanding resistance to anti-programmed cell death protein 1 (PD-1) therapy is critical for developing reversal strategies. Although ectonucleotidase CD39 (ENTPD1) (CD39) + cluster of differentiation 8 (CD8) + T cells have been associat…
Clinical
Selected reported efficacy
ORR 33.3%
Clinical
Reported ORR
33.3%
Clinical
Reported PFS
NA
Clinical
Reported OS
NA
Clinical
Result source
ClinicalTrials.gov NCT03294083
Clinical
Program phase
PHASE_3
Clinical
Trial activity
No active/completed counts
Clinical
Trial ref
NCT03294083