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 9건 · 타깃·모달리티 분포
활성 recruiting/enrolling 임상 · CT.gov completion 기준 · 상위 80건 표시
| 완료 예정 | 프로그램 | Phase | Status | Endpoint | 신뢰도 | NCT |
|---|---|---|---|---|---|---|
| 2026년 9월 | Tocilizumab | Phase 3 | Active, not recruiting | modified Rankin Scale (mRS) score at 90 days | 신뢰 높음 | NCT07263776 |
| 2026년 9월 | Tecvayli (teclistamab) | N/A | Not yet recruiting | Pain perception during local anesthetic injection | 보통 | NCT07124052 |
| 2026년 9월 | Talquetamab | — | Recruiting | Describe Baseline Characteristics of Participants with Relapsed/Refractory Multiple Myeloma (RRMM) who Received Teclistamab/ Talquetamab Outside of Clinical Trials; Overall Response Rate (ORR) in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Time to First Response in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Time to Best Response in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Duration of Response (DOR) in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Minimal Residue Assessment (MRD) in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Overall Survival (OS) in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Progression Free Survival (PFS) in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Time to Next Treatment (TTNT) in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Describe the Safety Management of Teclistamab/Talquetamab in the Treatment of Participants with RRMM Outside of Clinical Trials | 신뢰 높음 | NCT06285318 |
| 2026년 9월 | Darzalex (daratumumab) | Phase 2 | Active, not recruiting | Efficacy of daratumumab in inducing complete(CR) or partial(PR) renal remission in patients with active class III or IV Lupus Nephritis; Efficacy of daratumumab in inducing complete(CR) or partial(PR) | 보통 | NCT04868838 |
| 2026년 9월 | Darzalex (daratumumab) | Phase 1, Phase 2 | Recruiting | Number of Participants with Dose Limiting Toxicities (DLT) (Phase 1); Hematologic ≥ Very Good Partial Response (VGPR) Rate (Phase 2) | 신뢰 높음 | NCT05451771 |
| 2026년 9월 | Isatuximab | Phase 2 | Active, not recruiting | MRD negativity | 신뢰 높음 | NCT03104842 |
| 2026년 9월 | Darzalex (daratumumab) | Phase 1 | Active, not recruiting | Number of Participants with Treatment Related Adverse Events as Assessed by CTCAE v5.0 | 보통 | NCT07042594 |
| 2026년 9월 | Darzalex (daratumumab) | Phase 2 | Active, not recruiting | Best Overall Response | 신뢰 높음 | NCT03290950 |
| 2026년 9월 | Darzalex (daratumumab) | Phase 2 | Active, not recruiting | Deep clinical response | 신뢰 높음 | NCT06169215 |
modified Rankin Scale (mRS) score at 90 days
NCT07263776Pain perception during local anesthetic injection
NCT07124052Describe Baseline Characteristics of Participants with Relapsed/Refractory Multiple Myeloma (RRMM) who Received Teclistamab/ Talquetamab Outside of Clinical Trials; Overall Response Rate (ORR) in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Time to First Response in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Time to Best Response in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Duration of Response (DOR) in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Minimal Residue Assessment (MRD) in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Overall Survival (OS) in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Progression Free Survival (PFS) in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Time to Next Treatment (TTNT) in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Describe the Safety Management of Teclistamab/Talquetamab in the Treatment of Participants with RRMM Outside of Clinical Trials
NCT06285318Efficacy of daratumumab in inducing complete(CR) or partial(PR) renal remission in patients with active class III or IV Lupus Nephritis; Efficacy of daratumumab in inducing complete(CR) or partial(PR)
NCT04868838Number of Participants with Dose Limiting Toxicities (DLT) (Phase 1); Hematologic ≥ Very Good Partial Response (VGPR) Rate (Phase 2)
NCT05451771MRD negativity
NCT03104842Number of Participants with Treatment Related Adverse Events as Assessed by CTCAE v5.0
NCT07042594Best Overall Response
NCT03290950Deep clinical response
NCT06169215향후 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 9건 · 타깃·모달리티 분포
활성 recruiting/enrolling 임상 · CT.gov completion 기준 · 상위 80건 표시
| 완료 예정 | 프로그램 | Phase | Status | Endpoint | 신뢰도 | NCT |
|---|---|---|---|---|---|---|
| 2026년 9월 | Tocilizumab | Phase 3 | Active, not recruiting | modified Rankin Scale (mRS) score at 90 days | 신뢰 높음 | NCT07263776 |
| 2026년 9월 | Tecvayli (teclistamab) | N/A | Not yet recruiting | Pain perception during local anesthetic injection | 보통 | NCT07124052 |
| 2026년 9월 | Talquetamab | — | Recruiting | Describe Baseline Characteristics of Participants with Relapsed/Refractory Multiple Myeloma (RRMM) who Received Teclistamab/ Talquetamab Outside of Clinical Trials; Overall Response Rate (ORR) in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Time to First Response in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Time to Best Response in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Duration of Response (DOR) in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Minimal Residue Assessment (MRD) in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Overall Survival (OS) in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Progression Free Survival (PFS) in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Time to Next Treatment (TTNT) in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Describe the Safety Management of Teclistamab/Talquetamab in the Treatment of Participants with RRMM Outside of Clinical Trials | 신뢰 높음 | NCT06285318 |
| 2026년 9월 | Darzalex (daratumumab) | Phase 2 | Active, not recruiting | Efficacy of daratumumab in inducing complete(CR) or partial(PR) renal remission in patients with active class III or IV Lupus Nephritis; Efficacy of daratumumab in inducing complete(CR) or partial(PR) | 보통 | NCT04868838 |
| 2026년 9월 | Darzalex (daratumumab) | Phase 1, Phase 2 | Recruiting | Number of Participants with Dose Limiting Toxicities (DLT) (Phase 1); Hematologic ≥ Very Good Partial Response (VGPR) Rate (Phase 2) | 신뢰 높음 | NCT05451771 |
| 2026년 9월 | Isatuximab | Phase 2 | Active, not recruiting | MRD negativity | 신뢰 높음 | NCT03104842 |
| 2026년 9월 | Darzalex (daratumumab) | Phase 1 | Active, not recruiting | Number of Participants with Treatment Related Adverse Events as Assessed by CTCAE v5.0 | 보통 | NCT07042594 |
| 2026년 9월 | Darzalex (daratumumab) | Phase 2 | Active, not recruiting | Best Overall Response | 신뢰 높음 | NCT03290950 |
| 2026년 9월 | Darzalex (daratumumab) | Phase 2 | Active, not recruiting | Deep clinical response | 신뢰 높음 | NCT06169215 |
modified Rankin Scale (mRS) score at 90 days
NCT07263776Pain perception during local anesthetic injection
NCT07124052Describe Baseline Characteristics of Participants with Relapsed/Refractory Multiple Myeloma (RRMM) who Received Teclistamab/ Talquetamab Outside of Clinical Trials; Overall Response Rate (ORR) in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Time to First Response in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Time to Best Response in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Duration of Response (DOR) in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Minimal Residue Assessment (MRD) in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Overall Survival (OS) in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Progression Free Survival (PFS) in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Time to Next Treatment (TTNT) in Participants with RRMM who Received Teclistamab/Talquetamab Outside of Clinical Trials; Describe the Safety Management of Teclistamab/Talquetamab in the Treatment of Participants with RRMM Outside of Clinical Trials
NCT06285318Efficacy of daratumumab in inducing complete(CR) or partial(PR) renal remission in patients with active class III or IV Lupus Nephritis; Efficacy of daratumumab in inducing complete(CR) or partial(PR)
NCT04868838Number of Participants with Dose Limiting Toxicities (DLT) (Phase 1); Hematologic ≥ Very Good Partial Response (VGPR) Rate (Phase 2)
NCT05451771MRD negativity
NCT03104842Number of Participants with Treatment Related Adverse Events as Assessed by CTCAE v5.0
NCT07042594Best Overall Response
NCT03290950Deep clinical response
NCT06169215