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타깃 · 모달리티 · 임상 근거 · 비임상 맥락으로 최대 5개 프로그램을 나란히 비교합니다. · 다음 갱신 D-5 · 마지막 9월 2일

현재 선택: 5 · 임상 갱신 필요 5

프로그램 상세에서 관심 등록 후 2개 이상 모으면 여기서 한 번에 비교할 수 있습니다.

API CSV27행 · 5개 프로그램

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항목
ADCStandard DatabasestalePhase 2
Zilovertamab vedotin (Zilovertamab vedotin)
Merck Sharp & Dohme LLC·HER2
10 trials
AntibodyLimited DatastalePhase 1
Utomilumab (Utomilumab)
Kite, A Gilead Company·HER2
17 trials
AntibodyLimited DatastalePhase 3
lymphodepleting chemotherapy (lymphodepleting chemotherapy)
Hemogenyx Pharmaceuticals LLC·Non-Hodgkin Lymphoma
119 trials
CGTLimited DatastalePhase 1
FT500 (FT500)
Fate Therapeutics·HER2
2 trials
AntibodyLimited DatastalePhase 2
Akt inhibitor MK2206 (Akt inhibitor MK2206)
National Cancer Institute (NCI)·HER2
1 trials
Overview
Program
Zilovertamab vedotinUtomilumablymphodepleting chemotherapyFT500Akt inhibitor MK2206
Overview
Company
Merck Sharp & Dohme LLCKite, A Gilead CompanyHemogenyx Pharmaceuticals LLCFate TherapeuticsNational Cancer Institute (NCI)
Overview
Modality
ADCANTIBODYANTIBODYCGTANTIBODY
Overview
Target
HER2HER2Non-Hodgkin LymphomaHER2HER2
Overview
Indication
Lymphoma, Large B-Cell, DiffuseRelapsed/Refractory Large B-cell LymphomaBreast Cancer (Locally Advanced or Metastatic); HER2-positive Breast CancerAdvanced Solid Tumors; LymphomaChronic Lymphocytic Leukemia; Recurrent Small Lymphocytic Lymphoma
Overview
Phase
PHASE_2PHASE_1PHASE_3PHASE_1PHASE_2
Overview
Status
ACTIVEACTIVEACTIVEACTIVEACTIVE
Overview
Content status
Standard DatabaseLimited DataLimited DataLimited DataLimited Data
Overview
Data Confidence
Data Confidence · MediumData Confidence · LowData Confidence · LowData Confidence · LowData Confidence · Low
Overview
Development Signal
Development Signal · EmergingDevelopment Signal · WatchDevelopment Signal · EmergingDevelopment Signal · WatchDevelopment Signal · Emerging
Overview
Approval status
InvestigationalInvestigationalInvestigationalInvestigationalInvestigational
MoA
Mechanism
CAR-T cell therapy for GAD65 antibody-mediated cerebellar ataxia
MoA
Biomarker
biomarkers exist to predict toxicity risk, underscoring the need for further research
PK/PD
Species
Mouse
PK/PD
Animal (cat.)
Human, Mouse
PK/PD
Experiment
Pd
Toxicology
Species
Mouse
Toxicology
Animal (cat.)
Human, Mouse
Toxicology
Major finding
ROR1-PI3K/AKT signaling drives adaptive resistance to cell cycle blockade in TP53 mutated ovarian cancer.. Drug resistance remains a major challenge to durable responses in ovarian cancer, the fifth leading cause of cancer-related death among women. In this study, we developed long-term resistant (lt-res, several months) pre-clinical models of two drugs inducing mitotic arrest in TP53-mutated cell…hepatotoxicity mediated by Fcγ receptors (FcγR) ligand-dependent CD137 activatithrombocytopenia) but achieved a best response of morphologic leukemia-free state on day 14 foll
Toxicology
CRS
ReportedReported
Clinical
Safety signal
ROR1-PI3K/AKT signaling drives adaptive resistance to cell cycle blockade in TP53 mutated ovarian cancer.. Drug resistance remains a major challenge to durable responses in ovarian cancer, the fifth leading cause of cancer-related death among women. In this study, we developed long-term resistant (lt-res, several months) pre-clinical models of two drugs inducing mitotic arrest in TP53-mutated cell…hepatotoxicity mediated by Fcγ receptors (FcγR) ligand-dependent CD137 activatithrombocytopenia) but achieved a best response of morphologic leukemia-free state on day 14 foll
Clinical
Selected reported efficacy
ORR 1.4%ORR 67%ORR 43.8%ORR 0.92%
Clinical
Reported ORR
1.4%67%43.8%0.92%
Clinical
Result source
ClinicalTrials.gov NCT04504916ClinicalTrials.gov NCT03704298ClinicalTrials.gov NCT02445248ClinicalTrials.gov NCT01369849
Clinical
Program phase
PHASE_2PHASE_1PHASE_3PHASE_1PHASE_2
Clinical
Trial activity
No active/completed counts
Clinical
Trial ref
NCT04504916NCT03704298NCT02445248NCT01369849