← 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 CSV28행 · 1개 프로그램

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

항목
AntibodyLimited DatastalePhase 2
autologous stem cell transplantation (autologous stem cell transplantation)
Legend Biotech USA Inc·Multiple Myeloma, Newly Diagnosed
93 trials
Overview
Program
autologous stem cell transplantation
Overview
Company
Legend Biotech USA Inc
Overview
Modality
ANTIBODY
Overview
Target
Multiple Myeloma, Newly Diagnosed
Overview
Indication
Hodgkin's Lymphoma; Non-Hodgkin's Lymphoma
Overview
Phase
PHASE_2
Overview
Status
RECRUITING
Overview
Content status
Limited Data
Overview
Data Confidence
Data Confidence · Low
Overview
Development Signal
Development Signal · Emerging
Overview
Approval status
Investigational
MoA
Mechanism
targeting, multireceptor
MoA
Biomarker
biomarker and therapeutic target
PK/PD
Species
Mouse
PK/PD
Animal (cat.)
Mouse
PK/PD
Experiment
PD
Toxicology
Animal (cat.)
Unknown
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…
Toxicology
CRS
Reported
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 73.33%
Clinical
Reported ORR
73.33%
Clinical
Reported PFS
71.8
Clinical
Reported OS
100
Clinical
Result source
ClinicalTrials.gov NCT02722941
Clinical
Program phase
PHASE_2
Clinical
Trial activity
No active/completed counts
Clinical
Trial ref
NCT02722941