구조모아 (StructureMoa)항암 chemical structure spider web
방문향후 6개월 내 primary completion 예정인 활성 임상과 큐레이션·승인 프로그램의 phase 분포입니다. CT.gov completion date 기반 추정이며 공식 readout 일정과 다를 수 있습니다. RSS
큐레이션·FDA·임상 3건 이상 프로그램 2029개 — catalyst 일정과 별도의 전체 파이프라인 스냅샷입니다.
향후 6개월 catalyst 5건 · 타깃·모달리티 분포
활성 recruiting/enrolling 임상 · CT.gov completion 기준 · 상위 80건 표시
| 완료 예정 | 프로그램 | Phase | Status | Endpoint | 신뢰도 | NCT |
|---|---|---|---|---|---|---|
| 2026년 9월 | Opdivo (nivolumab) | Phase 1 | Active, not recruiting | Number (and Percentage) of Outcome Responses After Receiving Nivolumab, Tacrolimus, and Prednisone | 보통 | NCT03816332 |
| 2026년 9월 | Opdivo (nivolumab) | N/A | Active, not recruiting | Explore the biomarkers to predict objective response (OR); Explore the biomarkers to predict objective response (OR); Explore the biomarkers to predict objective response (OR); Explore the biomarkers to predict progression-free survival (PFS); Explore the biomarkers to predict progression-free survival (PFS); Explore the biomarkers to predict progression-free survival (PFS); Explore the biomarkers to predict overall survival (OS); Explore the biomarkers to predict overall survival (OS); Explore the biomarkers to predict overall survival (OS) | 신뢰 높음 | NCT04603248 |
| 2026년 9월 | Opdivo (nivolumab) | Phase 2 | Active, not recruiting | number of patients with a response | 신뢰 높음 | NCT03282344 |
| 2026년 9월 | Opdivo (nivolumab) | Phase 2 | Recruiting | Number of Patients with a Pathologic Response | 보통 | NCT04933903 |
| 2026년 9월 | Opdivo (nivolumab) | Phase 1 | Active, not recruiting | Incidence of Treatment-Emergent Adverse Events [Safety and tolerability] of 131-I-MIBG, ch14.18/CHO and Nivolumab in paediatric patients | 보통 | NCT02914405 |
Number (and Percentage) of Outcome Responses After Receiving Nivolumab, Tacrolimus, and Prednisone
NCT03816332Explore the biomarkers to predict objective response (OR); Explore the biomarkers to predict objective response (OR); Explore the biomarkers to predict objective response (OR); Explore the biomarkers to predict progression-free survival (PFS); Explore the biomarkers to predict progression-free survival (PFS); Explore the biomarkers to predict progression-free survival (PFS); Explore the biomarkers to predict overall survival (OS); Explore the biomarkers to predict overall survival (OS); Explore the biomarkers to predict overall survival (OS)
NCT04603248number of patients with a response
NCT03282344Number of Patients with a Pathologic Response
NCT04933903Incidence of Treatment-Emergent Adverse Events [Safety and tolerability] of 131-I-MIBG, ch14.18/CHO and Nivolumab in paediatric patients
NCT02914405향후 6개월 내 primary completion 예정인 활성 임상과 큐레이션·승인 프로그램의 phase 분포입니다. CT.gov completion date 기반 추정이며 공식 readout 일정과 다를 수 있습니다. RSS
큐레이션·FDA·임상 3건 이상 프로그램 2029개 — catalyst 일정과 별도의 전체 파이프라인 스냅샷입니다.
향후 6개월 catalyst 5건 · 타깃·모달리티 분포
활성 recruiting/enrolling 임상 · CT.gov completion 기준 · 상위 80건 표시
| 완료 예정 | 프로그램 | Phase | Status | Endpoint | 신뢰도 | NCT |
|---|---|---|---|---|---|---|
| 2026년 9월 | Opdivo (nivolumab) | Phase 1 | Active, not recruiting | Number (and Percentage) of Outcome Responses After Receiving Nivolumab, Tacrolimus, and Prednisone | 보통 | NCT03816332 |
| 2026년 9월 | Opdivo (nivolumab) | N/A | Active, not recruiting | Explore the biomarkers to predict objective response (OR); Explore the biomarkers to predict objective response (OR); Explore the biomarkers to predict objective response (OR); Explore the biomarkers to predict progression-free survival (PFS); Explore the biomarkers to predict progression-free survival (PFS); Explore the biomarkers to predict progression-free survival (PFS); Explore the biomarkers to predict overall survival (OS); Explore the biomarkers to predict overall survival (OS); Explore the biomarkers to predict overall survival (OS) | 신뢰 높음 | NCT04603248 |
| 2026년 9월 | Opdivo (nivolumab) | Phase 2 | Active, not recruiting | number of patients with a response | 신뢰 높음 | NCT03282344 |
| 2026년 9월 | Opdivo (nivolumab) | Phase 2 | Recruiting | Number of Patients with a Pathologic Response | 보통 | NCT04933903 |
| 2026년 9월 | Opdivo (nivolumab) | Phase 1 | Active, not recruiting | Incidence of Treatment-Emergent Adverse Events [Safety and tolerability] of 131-I-MIBG, ch14.18/CHO and Nivolumab in paediatric patients | 보통 | NCT02914405 |
Number (and Percentage) of Outcome Responses After Receiving Nivolumab, Tacrolimus, and Prednisone
NCT03816332Explore the biomarkers to predict objective response (OR); Explore the biomarkers to predict objective response (OR); Explore the biomarkers to predict objective response (OR); Explore the biomarkers to predict progression-free survival (PFS); Explore the biomarkers to predict progression-free survival (PFS); Explore the biomarkers to predict progression-free survival (PFS); Explore the biomarkers to predict overall survival (OS); Explore the biomarkers to predict overall survival (OS); Explore the biomarkers to predict overall survival (OS)
NCT04603248number of patients with a response
NCT03282344Number of Patients with a Pathologic Response
NCT04933903Incidence of Treatment-Emergent Adverse Events [Safety and tolerability] of 131-I-MIBG, ch14.18/CHO and Nivolumab in paediatric patients
NCT02914405