← 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 CSV25행 · 1개 프로그램

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

항목
ADCStandard DatabasestalePhase 2
Gemtuzumab Ozogamicin (Gemtuzumab Ozogamicin)
Pfizer·Acute Myeloid Leukemia
78 trials
Overview
Program
Gemtuzumab Ozogamicin
Overview
Company
Pfizer
Overview
Modality
ADC
Overview
Target
Acute Myeloid Leukemia
Overview
Indication
Acute Myelogenous Leukemia; Myelodysplastic Syndrome
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
Technology
Linker
linker, or payload that have limited their development
MoA
Mechanism
targeting specific cell surface antigens, many ADCs have also been associated with unique toxicities related to the antigen
MoA
Biomarker
HER2-positive, HER2-low
PK/PD
Species
Mouse
PK/PD
Animal (cat.)
Mouse
PK/PD
Experiment
pharmacokinetic
Toxicology
Species
Mouse
Toxicology
Animal (cat.)
Mouse
Toxicology
Major finding
Antibody-drug conjugates in hematologic malignancies.. Antibody-drug conjugates (ADCs) represent an important therapeutic modality for the treatment of various hematologic malignancies. These include gemtuzumab ozogamicin and inotuzumab ozagamicin for acute leukemias; brentuximab vedotin, polatuzumab vedotin, and loncastuximab tesirine for lymphoid malignancies; and belantamab mafadotin for multip…
Clinical
Safety signal
Antibody-drug conjugates in hematologic malignancies.. Antibody-drug conjugates (ADCs) represent an important therapeutic modality for the treatment of various hematologic malignancies. These include gemtuzumab ozogamicin and inotuzumab ozagamicin for acute leukemias; brentuximab vedotin, polatuzumab vedotin, and loncastuximab tesirine for lymphoid malignancies; and belantamab mafadotin for multip…
Clinical
Reported OS
6.15
Clinical
Result source
ClinicalTrials.gov NCT04337138
Clinical
Program phase
PHASE_2
Clinical
Trial ref
NCT04337138