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API CSV24행 · 1개 프로그램

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항목
ADCLimited DatastalePhase 2
Neurokinin-1 receptor antagonist (Neurokinin-1 receptor antagonist)
Merck Sharp & Dohme LLC·Carcinoma, Non-Small-Cell Lung
45 trials·t½ 34 h
Overview
Program
Neurokinin-1 receptor antagonist
Overview
Company
Merck Sharp & Dohme LLC
Overview
Modality
ADC
Overview
Target
Carcinoma, Non-Small-Cell Lung
Overview
Indication
Carcinoma, Non-Small-Cell Lung
Overview
Phase
PHASE_2
Overview
Status
RECRUITING
Overview
Content status
Limited Data
Overview
Data Confidence
Data Confidence · Low
Overview
Development Signal
Development Signal · Emerging
Overview
Approval status
Investigational
MoA
Mechanism
targets beyond conventional monoaminergic approaches, focusing on sodium channels, Neuropeptide Y (NPY), Neurokinin 1 (NK1) receptors, P2 × 7 purinergic receptors, Sigma-1 receptor
MoA
Biomarker
biomarkers for patient stratification will be critical in the hitherto elusive goal of developing precision m
PK/PD
Half-life
34 h
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
Tradipitant: A Novel Neurokinin-1 Receptor Antagonist for Motion Sickness.. Motion sickness affects millions of people with common symptoms, including nausea and vomiting. Medications used for management of motion sickness since 1870 predominately have anticholinergics and antihistamines properties. For the past 40 years, there have been no advances in medication options for motion sickness until …
Clinical
Safety signal
Tradipitant: A Novel Neurokinin-1 Receptor Antagonist for Motion Sickness.. Motion sickness affects millions of people with common symptoms, including nausea and vomiting. Medications used for management of motion sickness since 1870 predominately have anticholinergics and antihistamines properties. For the past 40 years, there have been no advances in medication options for motion sickness until …
Clinical
Result source
ClinicalTrials.gov NCT00601172
Clinical
Program phase
PHASE_2
Clinical
Trial ref
NCT00601172