임상 한눈에 보기

• 2건의 ClinicalTrials.gov 임상 기록
• 임상시험 탭에서 enrollment 상위 목록을 불러올 수 있습니다
• 모집 중 1건 · 완료/종료 1건
• Phase: Phase 2 · Phase 1, Phase 2
• Status: Recruiting · Terminated
• 주요 endpoint: Determine whether adding experimental agents to standard neoadjuvant medications increases the probability of pathologic complete response (pCR) over standard neoadjuvant chemotherapy for each biomarker signature established at trial entry. · Establishing predictive and prognostic indices based on qualification and exploratory markers to predict pCR and residual cancer burden (RCB). · To determine three- and five-year relapse-free survival (RFS) and OS among the treatment arms. · To determine incidence of adverse events (AEs) · serious adverse events (SAEs)
• 등록 대상자(표본 합산): 약 5,136명
• 등록된 결과: ORR 0%
• 핵심: Primary Objectives: Dose Escalation: * To assess the incidence rate of dose-limiting toxicity (DLT) and to determine t…

수집된 임상 필드(phase, status, endpoint 등) 기반 자동 요약입니다.