- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07869836
BL-M07D1 (Trastuzumab Brengitecan T-bren) vs Standard of Care Platinum-based Chemotherapy (PBC) for HER2-expressing Metastatic Urothelial Cancer After Progression on Anti-PD-(L)1-based Therapy
A Phase 3 Open-Label, Randomized Controlled Trial of T-bren (BL M07D1) vs. Platinum-based Chemotherapy in Patients With HER2 Expressing Metastatic Urothelial Cancer With Disease Progression on or After Anti-PD-(L)1-based Therapy
The objective of the study is to evaluate the efficacy and safety of T-bren in participants with HER2 expressing metastatic UC with progression on or after anti-PD-(L)1-based therapy.
연구 개요
상태
정황
상세 설명
This study is a Global Phase 3, randomized, open-label, multicenter study of T-bren for the treatment of metastatic UC. This study will assess the efficacy and safety of T-bren versus PBC in adult participants with HER2-expressing UC after progression on anti-PD-(L)1-based therapy.
연구 유형
등록 (추정된)
단계
- 3단계
연락처 및 위치
연구 연락처
- 이름: Christine LaRock
- 전화번호: 425-453-6841
- 이메일: Christine.LaRock@systimmune.com
연구 장소
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Georgia
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Macon, Georgia, 미국, 31210
- 모병
- Central Georgia Cancer Center
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수석 연구원:
- Bradley Sumrall, MD
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연락하다:
- Mackenzie Sanders, Study Coordinators
- 전화번호: 478-743-7068
- 이메일: mackenzie.sanders@aoncology.com
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연락하다:
- Rachel Warfield, Study Coordinators
- 전화번호: 478-743-7068
- 이메일: rachel.warfield@aoncology.com
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-
참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- Histologically or cytologically documented metastatic or surgically unresectable transitional cell carcinoma (TCC) of the urothelium involving the renal pelvis, ureter, bladder, or urethra. Minor histologic variants (ie, <50% overall) are acceptable, provided that TCC is the dominant histology.
- Disease progression or recurrence during or following anti-PD-(L)1-based therapy.
- Fresh biopsy or archival tumor samples.
- Documented HER2 expression by central laboratory testing.
- Eligible to receive carboplatin or cisplatin in combination with gemcitabine.
- At least 1 measurable lesion based on RECIST v1.1.
- An Eastern Cooperative Oncology Group performance status (ECOG PS) of 0 to 1.
- Adequate organ function.
- Adequate coagulation parameters.
Exclusion Criteria:
- Prior topoisomerase inhibitor-based ADC therapy.
- Primary tumors in the central nervous system (CNS), active or untreated CNS metastases, or carcinomatous meningitis.
- Bladder cancers with small cell histology.
- Other prior or concurrent malignancies except for certain localized cancers or low-grade prostate cancer (if approved by sponsor), or other malignancy treated with curative intent with a disease-free interval of at least 3 years.
- Prior history of clinically significant bleeding, or perforation of the gastrointestinal tract within 6 months of randomization.
- Active autoimmune diseases and inflammatory diseases.
- History of noninfectious interstitial lung disease (ILD)/pneumonitis that required treatment with steroids, have current ILD/pneumonitis, or where suspected ILD/pneumonitis cannot be ruled out by imaging at Screening.
- Advanced/clinically significant lung disease (eg, poorly controlled chronic obstructive pulmonary disease or asthma, restrictive lung disease, or pulmonary hypertension) within 6 months prior to randomization.
- Known human immunodeficiency virus infection.
- Active hepatitis B virus (HBV) infection.
- Active hepatitis C virus (HCV) infection.
- Active or latent tuberculosis.
- Other protocol-specified inclusion/ exclusion criteria apply
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 하나의
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
실험적: Arm A, T-bren Dose Level 1
T-bren administered intravenously |
T-bren: Administered intravenously on day 1 of each 21-day cycle
다른 이름들:
|
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실험적: Arm B, T-bren Dose Level 2
T-bren administered intravenously |
TBren administered intravenously on day 1 of each 21-day cycle
다른 이름들:
|
|
활성 비교기: Arm C, Control Arm, Platinum-based Chemotherapy (PBC)
|
Gemcitabine administered intravenously on Day 1 and Day 8 of each 21-day cycle and Cisplatin or Carboplatin administered intravenously on Day 1 of each 21-day cycle |
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Progression-Free Survival (PFS)
기간: Approximately 5 years
|
Progression-Free Survival (PFS) by Blinded Independent Central Review (BICR) per RECIST v1.1 in the primary population |
Approximately 5 years
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Overall Survival (OS)
기간: Approximately 5 years
|
Overall Survival (OS) in primary population |
Approximately 5 years
|
|
Progression-Free Survival (PFS) in the ITT population
기간: Approximately 5 years
|
Progression-Free Survival (PFS) by BICR per RECIST v1.1 in the ITT (Intent-to-Treat) Population |
Approximately 5 years
|
|
Overall Survival (OS) in the ITT population
기간: Approximately 5 years
|
Approximately 5 years
|
|
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Progression-Free Survival (PFS) by Investigator Assessment
기간: Approximately 5 years
|
Progression-Free Survival (PFS) by Investigator Assessment per RECIST v1.1 |
Approximately 5 years
|
|
Objective Response Rate (ORR) per RECIST v1.1
기간: Approximately 5 years
|
Approximately 5 years
|
|
|
Disease Control Rate (DCR) per RECIST v1.1
기간: Approximately 5 years
|
Approximately 5 years
|
|
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Duration of Response (DOR) per RECIST v1.1
기간: Approximately 5 years
|
Approximately 5 years
|
|
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Time to Response (TTR) per RECIST v1.1
기간: Approximately 5 years
|
Approximately 5 years
|
|
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Adverse Events (AEs) and Serious Adverse Events (SAEs)
기간: Approximately 5 years
|
Approximately 5 years
|
공동 작업자 및 조사자
스폰서
수사관
- 연구 책임자: Jimmy Liu Zhao, MD, PhD, SystImmune Inc.
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- BL-M07D1-UC-301
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
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