← 홈

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 CSV27행 · 1개 프로그램

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

항목
AntibodyLimited DatastalePhase 3
Denosumab (Denosumab)
Amgen·Giant Cell Tumor of Bone
92 trials·t½ 25.4 h
Overview
Program
Denosumab
Overview
Company
Amgen
Overview
Modality
ANTIBODY
Overview
Target
Giant Cell Tumor of Bone
Overview
Indication
Postmenopausal Osteoporosis
Overview
Phase
PHASE_3
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
targeting RANKL (denosumab), pro-inflammatory cytokines (IL-17 inhibitors), and Wnt pathway
MoA
Biomarker
Biomarkers, and Emerging Therapies
PK/PD
Half-life
25.4 h
PK/PD
Species
Mouse, Rat, Rabbit
PK/PD
Animal (cat.)
Mouse, Rat, In vitro
PK/PD
Experiment
PD
Toxicology
Species
Mouse, Rat, Rabbit
Toxicology
Animal (cat.)
Rat, In vitro
Toxicology
Major finding
Cardiovascular Outcomes Associated with Romosozumab Versus Denosumab in Chronic Kidney Disease.. Background and Objective: Romosozumab carries a warning for potential severe cardiovascular events, while denosumab is widely used for osteoporosis but requires safety considerations in advanced chronic kidney disease (CKD). Given the limited direct real-world evidence comparing these treatments, in th…
Clinical
Safety signal
Cardiovascular Outcomes Associated with Romosozumab Versus Denosumab in Chronic Kidney Disease.. Background and Objective: Romosozumab carries a warning for potential severe cardiovascular events, while denosumab is widely used for osteoporosis but requires safety considerations in advanced chronic kidney disease (CKD). Given the limited direct real-world evidence comparing these treatments, in th…
Clinical
Selected reported efficacy
ORR 81.9%
Clinical
Reported ORR
81.9%
Clinical
Result source
ClinicalTrials.gov NCT01920568
Clinical
Program phase
PHASE_3
Clinical
Trial activity
No active/completed counts
Clinical
Trial ref
NCT01920568