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항목
ADCStandard DatabasestalePhase 2
BV (Induction with Brentuximab vedotin, Induction with Brentuximab vedotin (BV))
Seagen / Takeda·Hodgkin Lymphoma, Adult
119 trials
Overview
Program
Induction with Brentuximab vedotin (BV)
Overview
Company
Seagen / Takeda
Overview
Modality
ADC
Overview
Target
Hodgkin Lymphoma, Adult
Overview
Indication
Hodgkin Lymphoma, Adult
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
Payload
Vedotin: A Retrospective Cohort Study from a Te
MoA
Mechanism
Targeting the Urotensin II Receptor Pathway
MoA
Biomarker
biomarkers; however, these methods do not detect all HPV strains and are not applicable to HPV-negative tumor
PK/PD
Species
Mouse, Rat, The primary endpoint was safety
PK/PD
Animal (cat.)
Mouse, Rat, In vitro
PK/PD
Experiment
pharmacokinetic
Toxicology
Species
Mouse, Rat, The primary endpoint was safety
Toxicology
Animal (cat.)
Mouse, Rat, In vitro
Toxicology
Major finding
Safety and efficacy of sotorasib plus panitumumab and FOLFIRI for previously treated KRAS G12C-mutated metastatic colorectal cancer in the CodeBreaK 101 phase Ib study.. In the phase III CodeBreaK 300 trial (NCT05198934), the combination of sotorasib, a KRAS G12C inhibitor, and panitumumab improved clinical outcomes in patients with chemorefractory KRAS G12C-mutated metastatic colorectal cancer (m…
Clinical
Safety signal
Safety and efficacy of sotorasib plus panitumumab and FOLFIRI for previously treated KRAS G12C-mutated metastatic colorectal cancer in the CodeBreaK 101 phase Ib study.. In the phase III CodeBreaK 300 trial (NCT05198934), the combination of sotorasib, a KRAS G12C inhibitor, and panitumumab improved clinical outcomes in patients with chemorefractory KRAS G12C-mutated metastatic colorectal cancer (m…
Clinical
Selected reported efficacy
ORR 78.3%
Clinical
Reported ORR
78.3%
Clinical
Reported PFS
16.5
Clinical
Reported OS
NA
Clinical
Result source
ClinicalTrials.gov NCT02453594
Clinical
Program phase
PHASE_2
Clinical
Trial activity
No active/completed counts
Clinical
Trial ref
NCT02453594