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

현재 선택: 1 · 임상 갱신 필요 1

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

API CSV19행 · 1개 프로그램

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항목
AntibodyLimited DatastalePhase 2
Cetrelimab (Cetrelimab)
Janssen Research & Development, LL…·Neoplasms
20 trials
Overview
Program
Cetrelimab
Overview
Company
Janssen Research & Development, LLC
Overview
Modality
ANTIBODY
Overview
Target
Neoplasms
Overview
Indication
Carcinoma, Non-Small-Cell Lung
Overview
Phase
PHASE_2
Overview
Status
RECRUITING
Overview
Content status
Limited Data
Overview
Data Confidence
Data Confidence · Low
Overview
Development Signal
Development Signal · Emerging
Overview
Approval status
Investigational
Toxicology
Major finding
Erdafitinib or Erdafitinib Plus Cetrelimab for Patients With Metastatic Urothelial Carcinoma and FGFR Alterations: Final Results From the Phase II NORSE Study.. First-line treatment options for cisplatin-ineligible patients with metastatic urothelial cancer (mUC) are limited. We conducted a phase II study of erdafitinib, alone or with cetrelimab, in FGFR -altered mUC. Adults with mUC and select FG…
Toxicology
CRS
Reported
Clinical
Safety signal
Erdafitinib or Erdafitinib Plus Cetrelimab for Patients With Metastatic Urothelial Carcinoma and FGFR Alterations: Final Results From the Phase II NORSE Study.. First-line treatment options for cisplatin-ineligible patients with metastatic urothelial cancer (mUC) are limited. We conducted a phase II study of erdafitinib, alone or with cetrelimab, in FGFR -altered mUC. Adults with mUC and select FG…
Clinical
Selected reported efficacy
ORR 75%
Clinical
Reported ORR
75.0%
Clinical
Result source
ClinicalTrials.gov NCT03431350
Clinical
Program phase
PHASE_2
Clinical
Trial ref
NCT03431350