Becotatug Vedotin Plus Pucotenlimab for Advanced Biliary Tract Cancer, Phase II
Becotatug Vedotin Combined With Pucotenlimab in First-Line Treatment-Failed Advanced Biliary Tract Carcinoma: A Phase II Exploratory Clinical Study
Biliary tract carcinoma (BTC), including cholangiocarcinoma and gallbladder cancer, is a highly aggressive digestive system malignancy with limited treatment options after failure of first-line standard chemotherapy.
This open-label, single-arm, Phase II exploratory study aims to evaluate the efficacy and safety of Becotatug Vedotin combined with Pucotenlimab in patients with EGFR-positive advanced BTC who have failed first-line therapy. Participants will receive the combination regimen until the occurrence of disease progression, unacceptable toxicity, withdrawal of informed consent, death, pregnancy, investigator's decision to discontinue treatment, or study termination, whichever occurs first.The primary endpoint is objective response rate (ORR) assessed per RECIST v1.1. Secondary endpoints include progression-free survival (PFS), overall survival (OS), disease control rate (DCR), duration of response (DOR), and safety.
調査の概要
状態
研究の種類
入学 (推定)
段階
- フェーズ2
連絡先と場所
研究連絡先
- 名前:Huikai Li, MD
- 電話番号:86+18622228639
- メール:vianvianvip@163.com
参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- Age ≥ 18 years, male or female.
- Histologically or cytologically confirmed advanced biliary tract cancer (BTC), including intrahepatic cholangiocarcinoma (ICC), extrahepatic cholangiocarcinoma (ECC), and gallbladder cancer (GBC); recurrent biliary tract cancer is also eligible.
- EGFR expression positive by immunohistochemistry (IHC) (+, ++, or +++).
- Failed at least one line of standard systemic therapy.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
- Life expectancy ≥ 3 months.
- At least one measurable lesion per RECIST v1.1 on CT or MRI.
- Child-Pugh class A or B (<7 points).
Adequate organ function as defined below:
- Hematologic: Hemoglobin (Hb) ≥ 90 g/L; white blood cell count (WBC) ≥ lower limit of normal (LLN); absolute neutrophil count (ANC) ≥ 1.5 × 10⁹/L; platelet count ≥ 100 × 10⁹/L.
- Renal: Serum creatinine ≤ 1.5 × upper limit of normal (ULN); creatinine clearance (CrCl) ≥ 55 mL/min.
- Hepatic: Total bilirubin ≤ 1.5 × ULN; ALT and AST ≤ 2.5 × ULN (or ≤ 3 × ULN for total bilirubin and ≤ 5 × ULN for ALT/AST in patients with intrahepatic cholangiocarcinoma or liver metastases).
- Coagulation: International normalized ratio (INR) ≤ 1.5 × ULN; partial thromboplastin time (PTT) within normal range.
- No serious complications such as active gastrointestinal bleeding, perforation, jaundice, gastrointestinal obstruction, or fever (>38°C) not attributable to cancer.
- Females of childbearing potential must have a negative serum or urine pregnancy test within 7 days prior to enrollment, must not be breastfeeding, and must agree to use effective contraception during the study and for 6 months after the last dose. Male participants must agree to use effective contraception during the study and for 6 months after the last dose.
- Expected to have good compliance with protocol-specified follow-up for efficacy and safety assessments.
- Able to understand the study and willing to provide written informed consent.
Exclusion Criteria:
- Diagnosis of another primary malignancy within 5 years prior to enrollment, except for adequately treated carcinoma in situ or basal cell carcinoma of the skin.
- EGFR expression negative by IHC.
- Known central nervous system (CNS) metastases or carcinomatous meningitis, unless clinically stable for ≥ 4 weeks after radiotherapy or surgery and asymptomatic.
- Psychiatric or neurological disorders that compromise the ability to comply with study procedures.
- Prior treatment with MMAE-containing antibody-drug conjugate (ADC) therapy.
- Planned or previous organ or bone marrow transplantation.
- Active or history of autoimmune disease requiring systemic immunosuppressive therapy.
- Receipt of live vaccine within 30 days prior to first dose. Inactivated seasonal influenza vaccines are allowed.
- Uncontrolled cardiac conditions or symptoms.
- Active infection or fever (unless clearly attributable to tumor).
- History or evidence of interstitial lung disease or active non-infectious pneumonitis.
- Any other condition that makes the patient unsuitable for enrollment, including but not limited to: immunodeficiency; active tuberculosis; hepatitis B (eligible if HBV-DNA < 500 IU/mL with normal liver function after antiviral therapy); hepatitis C virus (HCV) infection; uncorrectable electrolyte disturbances; uncontrolled pericardial effusion, pleural effusion, or ascites.
- Known hypersensitivity to any component of the study drugs.
- Use of systemic immunosuppressive agents or corticosteroids (> 10 mg/day prednisone equivalent) within 14 days prior to enrollment.
- Receipt of radiotherapy, chemotherapy, targeted therapy, or immunotherapy within 4 weeks prior to enrollment.
- Participation in another interventional clinical trial within 4 weeks prior to enrollment.
- Pregnancy or breastfeeding.
- Any other condition that, in the investigator's judgment, makes the patient inappropriate for study participation.
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:なし
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:Becotatug Vedotin + Pucotenlimab
The combination regimen will be continued until the occurrence of disease progression, unacceptable toxicity, withdrawal of informed consent, death, pregnancy, investigator's decision to discontinue treatment, or study termination, whichever occurs first.
|
2.0mg/kg ,IV,D1,Q3W;The infusion duration is 60 minutes ± 15 minutes, with the first infusion lasting no less than 60 minutes.
他の名前:
200mg,IV,D1,Q3W;The infusion duration is 60 minutes ± 15 minutes, with the first infusion lasting no less than 60 minutes.
他の名前:
|
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 |
|---|---|---|
|
Objective Response Rate (ORR)
時間枠:From start of treatment until disease progression, assessed up to 36 months.
|
Objective response rate is defined as the proportion of patients achieving complete response (CR) or partial response (PR) assessed per RECIST v1.1.
|
From start of treatment until disease progression, assessed up to 36 months.
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Progression-Free Survival (PFS)
時間枠:From start of treatment to disease progression or death, assessed up to 36 months.
|
Time from the first dose of study treatment to the first documented disease progression per RECIST v1.1 or death from any cause, whichever occurs first.
|
From start of treatment to disease progression or death, assessed up to 36 months.
|
|
Overall Survival (OS)
時間枠:From start of treatment to death, assessed up to 36 months.
|
Time from the first dose of study treatment to death from any cause.
|
From start of treatment to death, assessed up to 36 months.
|
|
Disease Control Rate (DCR)
時間枠:From start of treatment until disease progression, assessed up to 36 months.
|
Proportion of patients achieving complete response (CR), partial response (PR), or stable disease (SD) per RECIST v1.1.
|
From start of treatment until disease progression, assessed up to 36 months.
|
|
Duration of Response (DOR)
時間枠:From first response to disease progression or death, assessed up to 24 months from response.
|
Time from the first documented objective response (CR or PR) to the first documented disease progression per RECIST v1.1 or death from any cause, whichever occurs first.
|
From first response to disease progression or death, assessed up to 24 months from response.
|
|
Safety and Tolerability
時間枠:From first dose of study drug until 30 days after last dose, up to 36 months
|
Incidence, nature, and severity of adverse events (AEs) and serious adverse events (SAEs) assessed by NCI CTCAE v5.0.
|
From first dose of study drug until 30 days after last dose, up to 36 months
|
協力者と研究者
スポンサー
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
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。
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