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프로그램 비교

타깃 · 모달리티 · 임상 근거 · 비임상 맥락으로 최대 5개 프로그램을 나란히 비교합니다. · 다음 갱신 D-5 · 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 CSV29행 · 1개 프로그램

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항목
ADCStandard DatabasestalePhase 2
Fixed dose (Patritumab Deruxtecan, Patritumab Deruxtecan (Fixed dose))
Daiichi Sankyo Co., Ltd.·Non-Small Cell Lung Cancer Metasta…
149 trials·t½ 53 h
Overview
Program
Patritumab Deruxtecan (Fixed dose)
Overview
Company
Daiichi Sankyo Co., Ltd.
Overview
Modality
ADC
Overview
Target
Non-Small Cell Lung Cancer Metastatic
Overview
Indication
Non-Small Cell Lung Cancer Metastatic; Non-Small Cell Lung Cancer With Mutation in Epidermal Growth Factor Receptor
Overview
Phase
PHASE_2
Overview
Status
RECRUITING
Overview
Content status
Standard Database
Overview
Data Confidence
Data Confidence · Medium
Overview
Development Signal
Development Signal · Emerging
Overview
Approval status
Investigational
MoA
Mechanism
inhibits human epidermal growth factor receptor 2 (HER2) while sparing wild-type epidermal growth factor receptor
MoA
Biomarker
Biomarker of Methylthioadenosine Phosphorylase-Selective Protein Arginine Methyltransferase 5 Inhibition
PK/PD
Half-life
53 h
PK/PD
Species
Mouse
PK/PD
Animal (cat.)
Mouse, In vitro
PK/PD
Experiment
Pharmacokinetic
Toxicology
Species
Mouse
Toxicology
Animal (cat.)
Mouse
Toxicology
Major finding
Analysis of Seriousness and Preventability of Adverse Drug Reactions in Patients at a Tertiary Care Teaching Hospital: A Case Series.. This case series describes three serious adverse drug reactions (ADRs) reported from tertiary care teaching hospitals and analyses their seriousness and preventability. The cases included fixed drug eruption associated with paracetamol/amoxicillin exposure, Stevens…
Toxicology
CRS
Reported
Clinical
Safety signal
Analysis of Seriousness and Preventability of Adverse Drug Reactions in Patients at a Tertiary Care Teaching Hospital: A Case Series.. This case series describes three serious adverse drug reactions (ADRs) reported from tertiary care teaching hospitals and analyses their seriousness and preventability. The cases included fixed drug eruption associated with paracetamol/amoxicillin exposure, Stevens…
Clinical
Selected reported efficacy
ORR 64%
Clinical
Reported ORR
56%
Clinical
Reported PFS
5.5
Clinical
Result source
ClinicalTrials.gov NCT04619004
Clinical
Program phase
PHASE_2
Clinical
Trial activity
No active/completed counts
Clinical
Trial ref
NCT04619004