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타깃 · 모달리티 · 임상 근거 · 비임상 맥락으로 최대 5개 프로그램을 나란히 비교합니다. · 다음 갱신 D-5 · 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 1
DP2 (DS-8201a, DS-8201a (DP2))
Daiichi Sankyo / AstraZeneca·Advanced Solid Tumors
92 trials·t½ 100 days
Overview
Program
DS-8201a (DP2)
Overview
Company
Daiichi Sankyo / AstraZeneca
Overview
Modality
ANTIBODY
Overview
Target
Advanced Solid Tumors
Overview
Indication
Advanced Solid Tumors
Overview
Phase
PHASE_1
Overview
Status
ACTIVE
Overview
Content status
Limited Data
Overview
Data Confidence
Data Confidence · Low
Overview
Development Signal
Development Signal · Watch
Overview
Approval status
Investigational
MoA
Biomarker
biomarker can inform prognostic decisions in patients at high risk for death from withdrawal of life-sustaini
PK/PD
Half-life
100 days
PK/PD
Species
Mouse
PK/PD
Animal (cat.)
Mouse, In vitro
PK/PD
Experiment
PK
Toxicology
Species
Mouse
Toxicology
Animal (cat.)
Mouse, In vitro
Toxicology
Major finding
Cinchonidine, a Natural Quinoline Alkaloid, Attenuates Ischemic Neurovascular Injury Through Blood-Brain Barrier Preservation.. Background/Objectives : Ischemic stroke remains a major global health challenge, yet therapeutic options are severely restricted by narrow treatment windows and the risk of hemorrhagic transformation. Natural small molecules represent a valuable reservoir for discovering …
Toxicology
CRS
Reported
Clinical
Safety signal
Cinchonidine, a Natural Quinoline Alkaloid, Attenuates Ischemic Neurovascular Injury Through Blood-Brain Barrier Preservation.. Background/Objectives : Ischemic stroke remains a major global health challenge, yet therapeutic options are severely restricted by narrow treatment windows and the risk of hemorrhagic transformation. Natural small molecules represent a valuable reservoir for discovering …
Clinical
Selected reported efficacy
ORR 79.7%
Clinical
Reported ORR
79.7%
Clinical
Reported PFS
NA
Clinical
Reported OS
NA
Clinical
Result source
ClinicalTrials.gov NCT03529110
Clinical
Program phase
PHASE_1
Clinical
Trial activity
No active/completed counts
Clinical
Trial ref
NCT03529110
DS-8201a (DP2) 비교 | 바이오정보모아