구조모아 (StructureMoa)항암 chemical structure spider web
방문타깃 · 모달리티 · 임상 근거 · 비임상 맥락으로 최대 5개 프로그램을 나란히 비교합니다. · 다음 갱신 D-6 · 마지막 9월 2일
현재 선택: 2개 · 임상 갱신 필요 1개
프로그램 상세에서 관심 등록 후 2개 이상 모으면 여기서 한 번에 비교할 수 있습니다.
표가 넓으면 좌우로 스크롤하세요. 핵심 비교 모드에서는 중요 항목만 표시됩니다.
| 항목 | ||
|---|---|---|
Overview Program | Dupixent (dupilumab) | Stopping dupilumab |
Overview Company | Sanofi / Regeneron | Sanofi / Regeneron |
Overview Modality | ANTIBODY | ANTIBODY |
Overview Target | IL-4Rα | Severe Asthma |
Overview Indication | Atopic dermatitis, asthma, CRSwNP, EoE, prurigo nodularis | Severe Asthma |
Overview Phase | APPROVED | APPROVED |
Overview Status | APPROVED | RECRUITING |
Overview Content status | Curated Core | Limited Data |
Overview Data Confidence | Data Confidence · High | Data Confidence · Low |
Overview Development Signal | Development Signal · Established | Development Signal · Established |
Overview Approval status | FDA approved | Approved (flag incomplete) |
Positioning Key differentiator | Novel targets under investigation include MRGPRs, PARs, KIT receptors, OX-40, and sodium channels | — |
Positioning Known limitation | Non-Type 2 inflammation and inadequate trough levels. | — |
MoA Mechanism | Dupilumab binds IL-4Rα subunit shared by IL-4 type I and IL-13 type II receptors, inhibiting IL-4 and IL-13 signaling, reducing Type 2 inflammation (IgE, eosinophils, Th2 cytokines). | — |
MoA Biomarker | biomarkers and clinical characteristics and highlight the need for standardized, methodologically rigorous fu | — |
PK/PD Half-life | ~14 days (300 mg q2w) | — |
PK/PD Species | Mouse, EASI-75, peak pruritus NRS reduction | — |
PK/PD Animal (cat.) | Mouse | — |
PK/PD Experiment | PD | — |
Toxicology Species | Mouse | — |
Toxicology Major finding | Conjunctivitis, injection-site reactions, eosinophilia; herpes zoster caution. | — |
Toxicology CRS | N/A | — |
Clinical Safety signal | Conjunctivitis, injection-site reactions, eosinophilia; herpes zoster caution. | — |
Clinical Result source | ClinicalTrials.gov NCT02912468 | — |
Clinical Program phase | APPROVED | APPROVED |
Clinical Trial activity | No active/completed counts | — |
Clinical Trial ref | NCT02912468 | — |
타깃 · 모달리티 · 임상 근거 · 비임상 맥락으로 최대 5개 프로그램을 나란히 비교합니다. · 다음 갱신 D-6 · 마지막 9월 2일
현재 선택: 2개 · 임상 갱신 필요 1개
프로그램 상세에서 관심 등록 후 2개 이상 모으면 여기서 한 번에 비교할 수 있습니다.
표가 넓으면 좌우로 스크롤하세요. 핵심 비교 모드에서는 중요 항목만 표시됩니다.
| 항목 | ||
|---|---|---|
Overview Program | Dupixent (dupilumab) | Stopping dupilumab |
Overview Company | Sanofi / Regeneron | Sanofi / Regeneron |
Overview Modality | ANTIBODY | ANTIBODY |
Overview Target | IL-4Rα | Severe Asthma |
Overview Indication | Atopic dermatitis, asthma, CRSwNP, EoE, prurigo nodularis | Severe Asthma |
Overview Phase | APPROVED | APPROVED |
Overview Status | APPROVED | RECRUITING |
Overview Content status | Curated Core | Limited Data |
Overview Data Confidence | Data Confidence · High | Data Confidence · Low |
Overview Development Signal | Development Signal · Established | Development Signal · Established |
Overview Approval status | FDA approved | Approved (flag incomplete) |
Positioning Key differentiator | Novel targets under investigation include MRGPRs, PARs, KIT receptors, OX-40, and sodium channels | — |
Positioning Known limitation | Non-Type 2 inflammation and inadequate trough levels. | — |
MoA Mechanism | Dupilumab binds IL-4Rα subunit shared by IL-4 type I and IL-13 type II receptors, inhibiting IL-4 and IL-13 signaling, reducing Type 2 inflammation (IgE, eosinophils, Th2 cytokines). | — |
MoA Biomarker | biomarkers and clinical characteristics and highlight the need for standardized, methodologically rigorous fu | — |
PK/PD Half-life | ~14 days (300 mg q2w) | — |
PK/PD Species | Mouse, EASI-75, peak pruritus NRS reduction | — |
PK/PD Animal (cat.) | Mouse | — |
PK/PD Experiment | PD | — |
Toxicology Species | Mouse | — |
Toxicology Major finding | Conjunctivitis, injection-site reactions, eosinophilia; herpes zoster caution. | — |
Toxicology CRS | N/A | — |
Clinical Safety signal | Conjunctivitis, injection-site reactions, eosinophilia; herpes zoster caution. | — |
Clinical Result source | ClinicalTrials.gov NCT02912468 | — |
Clinical Program phase | APPROVED | APPROVED |
Clinical Trial activity | No active/completed counts | — |
Clinical Trial ref | NCT02912468 | — |
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