← 홈

프로그램 비교

타깃 · 모달리티 · 임상 근거 · 비임상 맥락으로 최대 5개 프로그램을 나란히 비교합니다. · 다음 갱신 D-6 · 마지막 9월 2일

현재 선택: 3 · 임상 갱신 필요 3 · Data Tier에서 열림

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

API CSV28행 · 3개 프로그램

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

항목
AntibodyLimited DatastalePhase 3
Mabthera (Mabthera)
Roche / Genentech·FRα
129 trials
AntibodyLimited DatastalePhase 2
Bendamustine Hydrochloride (Bendamustine Hydrochloride)
AbbVie·FRα
93 trials
AntibodyLimited DatastalePhase 2
tacrolimus (tacrolimus)
Tolera Therapeutics, Inc·FRα
168 trials·t½ 36 h
Overview
Program
MabtheraBendamustine Hydrochloridetacrolimus
Overview
Company
Roche / GenentechAbbVieTolera Therapeutics, Inc
Overview
Modality
ANTIBODYANTIBODYANTIBODY
Overview
Target
FRαFRαFRα
Overview
Indication
Relapsed Diffuse Large B-cell Lymphoma; Refractory Diffuse Large B-Cell LymphomaLymphoma, Mantle-CellLeukemia; Lymphoma
Overview
Phase
PHASE_3PHASE_2PHASE_2
Overview
Status
ACTIVERECRUITINGACTIVE
Overview
Content status
Limited DataLimited DataLimited Data
Overview
Data Confidence
Data Confidence · LowData Confidence · LowData Confidence · Low
Overview
Development Signal
Development Signal · EmergingDevelopment Signal · EmergingDevelopment Signal · Emerging
Overview
Approval status
InvestigationalInvestigationalInvestigational
MoA
Mechanism
bispecific antibodies to enhance macrophage-mediated cytotoxicity of B-cell lymphomaBendamustine is a bifunctional mechlorethamine derivative containing a purine-like benzimidazole ringTacrolimus binds to an intracellular protein, FKBP-12
MoA
Biomarker
CD20-positive, lowbiomarker data at diagnosis were included in the survival analysisbiomarkers of inflammation, and histopathological findings
PK/PD
Half-life
36 h
PK/PD
Species
Mouse, HumanRatMouse
PK/PD
Animal (cat.)
Human, Mouse, In vitroRat, In vitroMouse, In vitro
PK/PD
Experiment
pharmacodynamicpharmacokineticpharmacokinetic
Toxicology
Species
Mouse, HumanRatMouse
Toxicology
Animal (cat.)
Human, Mouse, In vitroRat, In vitroMouse
Toxicology
Major finding
interstitial lung disease, myositis, and arthritis, requiring immunosuppressive treatmentthrombocytopenia (16thrombocytopenia, microangiopathic hemolytic anemia, and progressive graft dysfunction
Toxicology
CRS
grade 3Reported
Clinical
Safety signal
interstitial lung disease, myositis, and arthritis, requiring immunosuppressive treatmentthrombocytopenia (16thrombocytopenia, microangiopathic hemolytic anemia, and progressive graft dysfunction
Clinical
Selected reported efficacy
ORR 84.7%ORR 75%ORR 4%
Clinical
Reported ORR
84.7%75%4%
Clinical
Result source
ClinicalTrials.gov NCT02268045ClinicalTrials.gov NCT01886872ClinicalTrials.gov NCT03816332
Clinical
Program phase
PHASE_3PHASE_2PHASE_2
Clinical
Trial activity
No active/completed countsNo active/completed countsNo active/completed counts
Clinical
Trial ref
NCT02268045NCT01886872NCT03816332