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

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항목
CGTStandard DatabasestalePhase 2
Recombinant Interferon Alfa (Recombinant Interferon Alfa)
SPP Pharmaclon Ltd.·Bladder Cancer
59 trials·t½ 57 h
Overview
Program
Recombinant Interferon Alfa
Overview
Company
SPP Pharmaclon Ltd.
Overview
Modality
CGT
Overview
Target
Bladder Cancer
Overview
Indication
Colorectal Cancer; Kidney Cancer
Overview
Phase
PHASE_2
Overview
Status
ACTIVE
Overview
Content status
Standard Database
Overview
Data Confidence
Data Confidence · Medium
Overview
Development Signal
Development Signal · Emerging
Overview
Approval status
Investigational
Technology
Vector
retroviral therapy on HIV reservoir clearance in acute HIV infection: study protocol for a
MoA
Mechanism
targets TIM3 on exhausted TILs and activates DCs via the IFNAR receptor
MoA
Biomarker
biomarkers for HBsAg clearance and responses to Peg-IFN-α in HBeAg-negative chronic hepatitis B patient
PK/PD
Half-life
57 h
PK/PD
Species
Mouse
PK/PD
Animal (cat.)
Mouse
PK/PD
Experiment
Pharmacokinetic
Toxicology
Species
Mouse
Toxicology
Animal (cat.)
Mouse
Toxicology
Major finding
Pharmacokinetics and Pharmacodynamics of Ropeginterferon Alfa-2b in Healthy Japanese and Caucasian Subjects After Single Subcutaneous Administration.. Ropeginterferon alfa-2b is a novel monopegylated recombinant interferon alfa-2b for the treatment of patients with polycythemia vera. The objectives of this study were to evaluate the pharmacokinetics, pharmacodynamics, safety, and tolerability of r…
Toxicology
CRS
Reported
Clinical
Safety signal
Pharmacokinetics and Pharmacodynamics of Ropeginterferon Alfa-2b in Healthy Japanese and Caucasian Subjects After Single Subcutaneous Administration.. Ropeginterferon alfa-2b is a novel monopegylated recombinant interferon alfa-2b for the treatment of patients with polycythemia vera. The objectives of this study were to evaluate the pharmacokinetics, pharmacodynamics, safety, and tolerability of r…
Clinical
Selected reported efficacy
ORR 32.4%
Clinical
Reported ORR
32.4%
Clinical
Result source
ClinicalTrials.gov NCT00738530
Clinical
Program phase
PHASE_2
Clinical
Trial ref
NCT00738530