← 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 CSV27행 · 1개 프로그램

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

항목
CGTStandard DatabasestalePhase 2
tamoxifen citrate (tamoxifen citrate)
Gamma Medica-Ideas·Breast Cancer
60 trials·t½ 7 h
Overview
Program
tamoxifen citrate
Overview
Company
Gamma Medica-Ideas
Overview
Modality
CGT
Overview
Target
Breast Cancer
Overview
Indication
Male Breast Cancer; Stage II Breast Cancer
Overview
Phase
PHASE_2
Overview
Status
ACTIVE
Overview
Content status
Standard Database
Overview
Data Confidence
Data Confidence · Medium
Overview
Development Signal
Development Signal · Emerging
Overview
Approval status
Investigational
Technology
Vector
lipid nanoparticles as a targeted chemotherapeutic drug
MoA
Mechanism
target genes in hyaloid endothelial cells, consistent with a role for GPR124 in mediating WNT/β-catenin signaling
MoA
Biomarker
HER2) negativity and a low
PK/PD
Half-life
7 h
PK/PD
Species
Mouse
PK/PD
Animal (cat.)
Mouse
PK/PD
Experiment
pharmacokinetic
Toxicology
Species
Mouse
Toxicology
Animal (cat.)
Mouse
Toxicology
Major finding
Human serum albumin-based polymeric nanoparticles for ratiometric co-encapsulation and co-delivery of palbociclib and tamoxifen citrate for synergistic effect in breast cancer management.. In conventional co-delivered chemotherapeutic strategies, the disparity in physicochemical properties and non-coordinated pharmacokinetic profile is largely overlooked. To overcome these long-standing challenges…
Clinical
Safety signal
Human serum albumin-based polymeric nanoparticles for ratiometric co-encapsulation and co-delivery of palbociclib and tamoxifen citrate for synergistic effect in breast cancer management.. In conventional co-delivered chemotherapeutic strategies, the disparity in physicochemical properties and non-coordinated pharmacokinetic profile is largely overlooked. To overcome these long-standing challenges…
Clinical
Selected reported efficacy
ORR 13%
Clinical
Reported ORR
13%
Clinical
Result source
ClinicalTrials.gov NCT02806544
Clinical
Program phase
PHASE_2
Clinical
Trial ref
NCT02806544