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

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API CSV29행 · 1개 프로그램

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항목
AntibodyCurated CorestalePhase 3
Ramucirumab (Ramucirumab)
Eli Lilly and Company·Non-Small Cell Lung Cancer
117 trials·t½ 14 h
Overview
Program
Ramucirumab
Overview
Company
Eli Lilly and Company
Overview
Modality
ANTIBODY
Overview
Target
Non-Small Cell Lung Cancer
Overview
Indication
Advanced Esophageal Adenocarcinoma; Advanced Gastric Adenocarcinoma
Overview
Phase
PHASE_3
Overview
Status
RECRUITING
Overview
Content status
Curated Core
Overview
Data Confidence
Data Confidence · High
Overview
Development Signal
Development Signal · Emerging
Overview
Approval status
Investigational
Positioning
Key differentiator
novel 5-exo-miRNA panel for predicting response to second-line PTX plus RAM therapy in gastric cancer
Positioning
Known limitation
resistance to VEGFR2 blockade
MoA
Mechanism
targets vascular endothelial growth factor receptor
MoA
Biomarker
biomarkers exist to predict therapeutic response
PK/PD
Half-life
14 h
PK/PD
Species
Mouse
PK/PD
Animal (cat.)
Mouse
PK/PD
Experiment
Biodistribution
Toxicology
Species
Mouse
Toxicology
Animal (cat.)
Mouse
Toxicology
Major finding
Risk factors of docetaxel-induced peripheral edema in non-small cell lung cancer treatment: a multi-institutional cohort study.. Peripheral edema is an adverse event associated with docetaxel (DTX). However, previous studies on DTX-induced peripheral edema have been limited to patients with breast cancer. Therefore, evaluation of symptoms in other cancer types is essential. We aimed to identify th…
Clinical
Safety signal
Risk factors of docetaxel-induced peripheral edema in non-small cell lung cancer treatment: a multi-institutional cohort study.. Peripheral edema is an adverse event associated with docetaxel (DTX). However, previous studies on DTX-induced peripheral edema have been limited to patients with breast cancer. Therefore, evaluation of symptoms in other cancer types is essential. We aimed to identify th…
Clinical
Selected reported efficacy
ORR 37.5%
Clinical
Reported ORR
37.5%
Clinical
Result source
ClinicalTrials.gov NCT04499924
Clinical
Program phase
PHASE_3
Clinical
Trial activity
No active/completed counts
Clinical
Trial ref
NCT04499924