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항목
ADCLimited DatastalePhase 2
Gemcitabine Hydrochloride (Gemcitabine Hydrochloride)
K-Group, Beta, Inc., a wholly owne…·FRα
165 trials
Overview
Program
Gemcitabine Hydrochloride
Overview
Company
K-Group, Beta, Inc., a wholly owned subsidiary of Zentalis Pharmaceuticals, Inc
Overview
Modality
ADC
Overview
Target
FRα
Overview
Indication
Fallopian Tube Carcinosarcoma; Fallopian Tube Clear Cell Adenocarcinoma
Overview
Phase
PHASE_2
Overview
Status
ACTIVE
Overview
Content status
Limited Data
Overview
Data Confidence
Data Confidence · Low
Overview
Development Signal
Development Signal · Emerging
Overview
Approval status
Investigational
Technology
Linker
linker-payload technologies
MoA
Mechanism
of ProAgio, which includes reducing hypoxia and modulating TME
MoA
Biomarker
HER2 expression
PK/PD
Species
Mouse
PK/PD
Animal (cat.)
Mouse, In vitro
PK/PD
Experiment
pharmacokinetic
Toxicology
Species
Mouse
Toxicology
Animal (cat.)
Mouse, In vitro
Toxicology
Major finding
From Parenteral to Oral Delivery: Facile Formulation of Oral Gemcitabine Nanospanlastics for Enhanced Bioavailability and Anticancer Activity in Murine Breast Cancer Model.. Gemcitabine hydrochloride (GEM) is a commonly used antineoplastic that is delivered only by intravenous infusion due to its limited oral bioavailability of 10%. The study aims to design and optimize novel Spanlastics (GEM-SLs)…
Clinical
Safety signal
From Parenteral to Oral Delivery: Facile Formulation of Oral Gemcitabine Nanospanlastics for Enhanced Bioavailability and Anticancer Activity in Murine Breast Cancer Model.. Gemcitabine hydrochloride (GEM) is a commonly used antineoplastic that is delivered only by intravenous infusion due to its limited oral bioavailability of 10%. The study aims to design and optimize novel Spanlastics (GEM-SLs)…
Clinical
Selected reported efficacy
41.6%
Clinical
Result source
ClinicalTrials.gov NCT04222972
Clinical
Program phase
PHASE_2
Clinical
Trial activity
No active/completed counts
Clinical
Trial ref
NCT04222972