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

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항목
ADCLimited DatastalePhase 2
Gemcitabine (Gemzar, Gemzar (Gemcitabine))
Amer Zureikat·Ovarian Neoplasms
91 trials
Overview
Program
Gemzar (Gemcitabine)
Overview
Company
Amer Zureikat
Overview
Modality
ADC
Overview
Target
Ovarian Neoplasms
Overview
Indication
Pancreatic Cancer
Overview
Phase
PHASE_2
Overview
Status
DISCONTINUED
Overview
Content status
Limited Data
Overview
Data Confidence
Data Confidence · Low
Overview
Development Signal
Development Signal · Emerging
Overview
Approval status
Investigational
Technology
Payload
vedotin after avelumab
Technology
Linker
linker-payload technologies
MoA
Mechanism
of ProAgio, which includes reducing hypoxia and modulating TME
MoA
Biomarker
biomarker-informed trials, rather than to identify a single preferred ICI strategy
PK/PD
Species
Rat
PK/PD
Animal (cat.)
Rat, In vitro
PK/PD
Experiment
PD
Toxicology
Species
Rat
Toxicology
Animal (cat.)
Rat, In vitro
Toxicology
Major finding
Mechanistic Insights Into Dose-Dependent Alleviation of Colorectal Cancer Through Artemisinin-Loaded Mesoporous Silica Nanoparticles in 1,2-Dimethylhydrazine-Induced Albino Wistar Rats.. The current study investigates the suitability of encapsulating the Artemisinin-plant-originated lipophilic drug molecule into polyethylene glycol-coated mesoporous silica nanoparticles in a suitable dose regimen …
Clinical
Safety signal
Mechanistic Insights Into Dose-Dependent Alleviation of Colorectal Cancer Through Artemisinin-Loaded Mesoporous Silica Nanoparticles in 1,2-Dimethylhydrazine-Induced Albino Wistar Rats.. The current study investigates the suitability of encapsulating the Artemisinin-plant-originated lipophilic drug molecule into polyethylene glycol-coated mesoporous silica nanoparticles in a suitable dose regimen …
Clinical
Selected reported efficacy
ORR 6%
Clinical
Reported ORR
6%
Clinical
Reported PFS
7.9
Clinical
Reported OS
13.9
Clinical
Result source
ClinicalTrials.gov NCT01524991
Clinical
Program phase
PHASE_2
Clinical
Trial activity
No active/completed counts
Clinical
Trial ref
NCT01524991