← 홈

프로그램 비교

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 CSV28행 · 1개 프로그램

표가 넓으면 좌우로 스크롤하세요. 핵심 비교 모드에서는 중요 항목만 표시됩니다.

항목
AntibodyLimited DatastalePhase 1
mutation analysis (mutation analysis)
Celgene·Kidney Cancer
95 trials
Overview
Program
mutation analysis
Overview
Company
Celgene
Overview
Modality
ANTIBODY
Overview
Target
Kidney Cancer
Overview
Indication
Leukemia
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
Mechanism
targets were identified for further protein-protein interaction (PPI) and enrichment analyses to investigate functional pathway
MoA
Biomarker
biomarker in lung adenocarcinoma and other human malignancies
PK/PD
Species
Mouse
PK/PD
Animal (cat.)
Mouse, In vitro
PK/PD
Experiment
PD
Toxicology
Species
Mouse
Toxicology
Animal (cat.)
Mouse
Toxicology
Major finding
OBP-Mediated Molecular Mechanism Underlying the Olfactory Repellent Effect of Mosla chinensis Essential Oil Against Culex quinquefasciatus .. Mosquitoes, including Culex quinquefasciatus and Aedes aegypti , are important vectors of dengue fever, Zika virus, West Nile virus, Japanese encephalitis virus, Eastern equine encephalitis virus, etc. Biological control has always been urgent in mosquito pr…
Clinical
Safety signal
OBP-Mediated Molecular Mechanism Underlying the Olfactory Repellent Effect of Mosla chinensis Essential Oil Against Culex quinquefasciatus .. Mosquitoes, including Culex quinquefasciatus and Aedes aegypti , are important vectors of dengue fever, Zika virus, West Nile virus, Japanese encephalitis virus, Eastern equine encephalitis virus, etc. Biological control has always been urgent in mosquito pr…
Clinical
Selected reported efficacy
ORR 67%
Clinical
Reported ORR
67%
Clinical
Reported PFS
11.9
Clinical
Reported OS
67
Clinical
Result source
ClinicalTrials.gov NCT02438722
Clinical
Program phase
PHASE_1
Clinical
Trial activity
No active/completed counts
Clinical
Trial ref
NCT02438722