← 홈

프로그램 비교

검색으로 10,000+ 프로그램 중 최대 5개를 골라 PK/PD · 독성 · 임상을 나란히 비교합니다. · 다음 갱신 D-8 · 마지막 7월 21일

현재 선택: 5 · 임상 갱신 필요 3

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

API CSV24행 · 5개 프로그램

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

항목
ADCFDAPhase 3
Polatuzumab Vedotin (Polatuzumab Vedotin)
Roche / Genentech·FRα
ORR 100%·t½ 12.2 h
ADCstalePhase 3
Pegfilgrastim (Pegfilgrastim)
Amgen·Ovarian Cancer
ORR 56.7%·t½ 80 days
ADCstalePhase 3
Osimertinib (Osimertinib)
Janssen Research & Development, LL…·FRα
ORR 76.7%·t½ 48 h
ADCstalePhase 2
Binimetinib (Binimetinib)
Pfizer·FRα
ORR 66.7%·t½ 64 h
ADCPhase 3
Gemcitabine Hydrochloride (Gemcitabine Hydrochloride)
K-Group, Beta, Inc., a wholly owne…·FRα
ORR 0.4%
Overview
Program
Polatuzumab VedotinPegfilgrastimOsimertinibBinimetinibGemcitabine Hydrochloride
Overview
Company
Roche / GenentechAmgenJanssen Research & Development, LLCPfizerK-Group, Beta, Inc., a wholly owned subsidiary of Zentalis Pharmaceuticals, Inc
Overview
Modality
ADCADCADCADCADC
Overview
Target
FRαOvarian CancerFRαFRαFRα
Overview
Indication
Relapsed or Refractory Follicular Lymphoma, Relapsed or Refractory Diffuse Large B-Cell LymphomaCancer; Colon CancerCarcinoma, Non-Small-Cell LungCancerClear Cell Adenocarcinoma; Fallopian Tube Clear Cell Adenocarcinoma
Overview
Phase
PHASE_3PHASE_3PHASE_3PHASE_2PHASE_3
Overview
Status
RECRUITINGRECRUITINGRECRUITINGRECRUITINGRECRUITING
MoA
Mechanism
targeting specific cell surface antigens, many ADCs have also been associated with unique toxicities related to the antigenPegfilgrastim products are colony-stimulating factors that act on hematopoietic cells by binding to specific cell surface receptors, thereby stimulating proliferation, differentiation, commitment, and end cell functionacheckpoint inhibitor (ICI)-induced acute interstitial nephritis, who presented with acute-onset nausea, vomiting aof ProAgio, which includes reducing hypoxia and modulating TME
MoA
Biomarker
CD20 expressionPD-L1-highPD-L1 expressionHER2 expression
PK/PD
Half-life
12.2 h80 days48 h64 h
PK/PD
Species
RatCynomolgus monkey, NHPRatMouse
PK/PD
Animal (cat.)
Rat, In vitroHuman, NHPRat, In vitroMouse, In vitro
PK/PD
Experiment
pharmacokineticPharmacokineticPKpharmacokinetic
Toxicology
Species
Cynomolgus monkey, Mouse, RatCynomolgus monkey, NHP, RatRat, RabbitMouse
Toxicology
Animal (cat.)
Mouse, Rat, NHPRatRatMouse, In vitro
Toxicology
Major finding
Hepatotoxicity: Monitor liver enzymes and bilirubinThrombocytopenia: Monitor platelet count ( 5Interstitial Lung Disease (ILD)/Pneumonitis : Monitor for new or worsening pulmonary symptoms indHepatotoxicity: Monitor liver function tests before and during treatment with MEKTOVI and eFrom Parenteral to Oral Delivery: Facile Formulation of Oral Gemcitabine Nanospanlastics for Enhanced Bioavailability and Anticancer Activity in Murine Breast Cancer Model.. Gemcitabine hydrochloride (GEM) is a commonly used antineoplastic that is delivered only by intravenous infusion due to its limited oral bioavailability of 10%. The study aims to design and optimize novel Spanlastics (GEM-SLs)…
Clinical
Primary efficacy
ORR 100%ORR 56.7%ORR 76.7%ORR 66.7%ORR 0.4%
Clinical
ORR
100.0%56.7%76.7%66.7%0.4%
Clinical
PFS
10.1
Clinical
OS
24.6
Clinical
Result source
ClinicalTrials.gov NCT02611323ClinicalTrials.gov NCT00911170ClinicalTrials.gov NCT02296125ClinicalTrials.gov NCT01543698ClinicalTrials.gov NCT00942331
Clinical
Data Tier / Score
S · 92A · 70B · 69C · 57C · 41
Clinical
Program phase
PHASE_3PHASE_3PHASE_3PHASE_2PHASE_3
Clinical
Clinical sync
2026년 7월 18일 (8일 전)2026년 7월 6일 (21일 전 · 갱신 권장)2026년 7월 6일 (21일 전 · 갱신 권장)2026년 7월 9일 (18일 전 · 갱신 권장)2026년 7월 18일 (8일 전)