← 홈

프로그램 비교

타깃 · 모달리티 · 임상 근거 · 비임상 맥락으로 최대 5개 프로그램을 나란히 비교합니다. · 다음 갱신 D-6 · 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

표가 넓으면 좌우로 스크롤하세요. 핵심 비교 모드에서는 중요 항목만 표시됩니다.

항목
AntibodyLimited DatastalePhase 2
Doxil (Doxil)
Janssen Research & Development, LL…·Breast Cancer
94 trials·t½ 78.4 days
Overview
Program
Doxil
Overview
Company
Janssen Research & Development, LLC
Overview
Modality
ANTIBODY
Overview
Target
Breast Cancer
Overview
Indication
Breast Cancer; Leukemia
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
MoA
Mechanism
target multiple pathway
MoA
Biomarker
HER2-positive breast cancer models, including cell lines (CD44 high
PK/PD
Half-life
78.4 days
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
Radiolabeling of clinically approved nanomedicine carriers: lessons from albumin- and liposome-based systems for biomaterial design and translational imaging.. Radiolabeling is a powerful approach for investigating the in vivo behavior of nanomedicine carriers beyond conventional pharmacokinetic analysis. This review examines clinically approved nanocarrier platforms, particularly albumin-bound na…
Clinical
Safety signal
Radiolabeling of clinically approved nanomedicine carriers: lessons from albumin- and liposome-based systems for biomaterial design and translational imaging.. Radiolabeling is a powerful approach for investigating the in vivo behavior of nanomedicine carriers beyond conventional pharmacokinetic analysis. This review examines clinically approved nanocarrier platforms, particularly albumin-bound na…
Clinical
Selected reported efficacy
ORR 100%
Clinical
Reported ORR
100%
Clinical
Reported PFS
79
Clinical
Reported OS
98
Clinical
Result source
ClinicalTrials.gov NCT00822120
Clinical
Program phase
PHASE_2
Clinical
Trial activity
No active/completed counts
Clinical
Trial ref
NCT00822120