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.
調査の概要
状態
条件
詳細な説明
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.
研究の種類
入学 (推定)
段階
- フェーズ 3
連絡先と場所
研究連絡先
- 名前:Christine LaRock
- 電話番号:425-453-6841
- メール:Christine.LaRock@systimmune.com
研究場所
-
-
Georgia
-
Macon、Georgia、アメリカ、31210
- 募集
- Central Georgia Cancer Center
-
主任研究者:
- Bradley Sumrall, MD
-
コンタクト:
- Mackenzie Sanders, Study Coordinators
- 電話番号:478-743-7068
- メール:mackenzie.sanders@aoncology.com
-
コンタクト:
- Rachel Warfield, Study Coordinators
- 電話番号:478-743-7068
- メール:rachel.warfield@aoncology.com
-
-
参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
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
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:独身
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:Arm A, T-bren Dose Level 1
T-bren administered intravenously |
T-bren: Administered intravenously on day 1 of each 21-day cycle
他の名前:
|
|
実験的:Arm B, T-bren Dose Level 2
T-bren administered intravenously |
TBren administered intravenously on day 1 of each 21-day cycle
他の名前:
|
|
アクティブコンパレータ: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 |
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Progression-Free Survival (PFS)
時間枠:Approximately 5 years
|
Progression-Free Survival (PFS) by Blinded Independent Central Review (BICR) per RECIST v1.1 in the primary population |
Approximately 5 years
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Overall Survival (OS)
時間枠:Approximately 5 years
|
Overall Survival (OS) in primary population |
Approximately 5 years
|
|
Progression-Free Survival (PFS) in the ITT population
時間枠: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
時間枠:Approximately 5 years
|
Approximately 5 years
|
|
|
Progression-Free Survival (PFS) by Investigator Assessment
時間枠: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
時間枠:Approximately 5 years
|
Approximately 5 years
|
|
|
Disease Control Rate (DCR) per RECIST v1.1
時間枠:Approximately 5 years
|
Approximately 5 years
|
|
|
Duration of Response (DOR) per RECIST v1.1
時間枠:Approximately 5 years
|
Approximately 5 years
|
|
|
Time to Response (TTR) per RECIST v1.1
時間枠:Approximately 5 years
|
Approximately 5 years
|
|
|
Adverse Events (AEs) and Serious Adverse Events (SAEs)
時間枠:Approximately 5 years
|
Approximately 5 years
|
協力者と研究者
スポンサー
捜査官
- スタディディレクター:Jimmy Liu Zhao, MD, PhD、SystImmune Inc.
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- BL-M07D1-UC-301
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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