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항목
AntibodyLimited DatastalePhase 2
Anti-Thymocyte Globulin (Anti-Thymocyte Globulin)
Sumitomo Pharma Switzerland GmbH·End Stage Renal Disease
125 trials·t½ 3 h
Overview
Program
Anti-Thymocyte Globulin
Overview
Company
Sumitomo Pharma Switzerland GmbH
Overview
Modality
ANTIBODY
Overview
Target
End Stage Renal Disease
Overview
Indication
Leukemia; Lymphoma
Overview
Phase
PHASE_2
Overview
Status
ACTIVE
Overview
Content status
Limited Data
Overview
Data Confidence
Data Confidence · Low
Overview
Development Signal
Development Signal · Emerging
Overview
Approval status
Investigational
MoA
Mechanism
The mechanism of action by which polyclonal antilymphocyte preparations suppress immune responses is not fully understood
MoA
Biomarker
biomarkers
PK/PD
Half-life
3 h
PK/PD
Species
Rabbit, Human
PK/PD
Animal (cat.)
Human, In vitro
PK/PD
Experiment
pharmacokinetic
Toxicology
Species
Rabbit, Human
Toxicology
Animal (cat.)
Human, In vitro
Toxicology
Major finding
High Predicted Thiotepa Exposure is Associated with Increased Risk of Thrombotic Microangiopathy and Non-Relapse Mortality in Pediatric Patients Undergoing Alpha-Beta T-Cell Depleted Haploidentical Transplantation.. Thiotepa is commonly included in combination with other agents to prevent rejection and relapse following alpha-beta-T-cell/CD19-depleted (AB-TCD) haploidentical hematopoietic cell tra…
Toxicology
CRS
10%
Clinical
Safety signal
High Predicted Thiotepa Exposure is Associated with Increased Risk of Thrombotic Microangiopathy and Non-Relapse Mortality in Pediatric Patients Undergoing Alpha-Beta T-Cell Depleted Haploidentical Transplantation.. Thiotepa is commonly included in combination with other agents to prevent rejection and relapse following alpha-beta-T-cell/CD19-depleted (AB-TCD) haploidentical hematopoietic cell tra…
Clinical
Selected reported efficacy
ORR 32%
Clinical
Reported ORR
32%
Clinical
Result source
ClinicalTrials.gov NCT00822770
Clinical
Program phase
PHASE_2
Clinical
Trial activity
No active/completed counts
Clinical
Trial ref
NCT00822770