← 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
ADCLimited DatastalePhase 3
High Dose Chemotherapy (High Dose Chemotherapy)
Celgene·FRα
91 trials·t½ 47 h
Overview
Program
High Dose Chemotherapy
Overview
Company
Celgene
Overview
Modality
ADC
Overview
Target
FRα
Overview
Indication
Recurrent Classic Hodgkin Lymphoma; Refractory Classic Hodgkin Lymphoma
Overview
Phase
PHASE_3
Overview
Status
RECRUITING
Overview
Content status
Limited Data
Overview
Data Confidence
Data Confidence · Low
Overview
Development Signal
Development Signal · Emerging
Overview
Approval status
Investigational
Technology
Payload
vedotin (BV) maintenance therapy improves patie
MoA
Mechanism
targeting and cytotoxicity by coupling NK cells with tumor-specific antibodies targeting antigen
MoA
Biomarker
biomarkers are critical to predict which patients will require treatment escalation
PK/PD
Half-life
47 h
PK/PD
Species
Rat
PK/PD
Animal (cat.)
Rat, In vitro
PK/PD
Experiment
PD
Toxicology
Species
Rat
Toxicology
Animal (cat.)
Rat, In vitro
Toxicology
Major finding
Efficacy of anti-GD2 antibody immunotherapy with filgrastim and teceleukin versus standard treatment with sargramostim, aldesleukin and isotretinoin in children with high-risk neuroblastoma.. Granulocyte-macrophage colony-stimulating factor (GM-CSF), aldesleukin and isotretinoin are unavailable in Japan, necessitating alternative cytokines for dinutuximab immunotherapy. We compared the efficacy of…
Clinical
Safety signal
Efficacy of anti-GD2 antibody immunotherapy with filgrastim and teceleukin versus standard treatment with sargramostim, aldesleukin and isotretinoin in children with high-risk neuroblastoma.. Granulocyte-macrophage colony-stimulating factor (GM-CSF), aldesleukin and isotretinoin are unavailable in Japan, necessitating alternative cytokines for dinutuximab immunotherapy. We compared the efficacy of…
Clinical
Selected reported efficacy
ORR 29%
Clinical
Reported ORR
29%
Clinical
Result source
ClinicalTrials.gov NCT01182415
Clinical
Program phase
PHASE_3
Clinical
Trial ref
NCT01182415