- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07649980
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.
Studieoversigt
Status
Intervention / Behandling
Undersøgelsestype
Tilmelding (Anslået)
Fase
- Fase 2
Kontakter og lokationer
Studiekontakt
- Navn: Huikai Li, MD
- Telefonnummer: 86+18622228639
- E-mail: vianvianvip@163.com
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
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.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: 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.
Andre navne:
200mg,IV,D1,Q3W;The infusion duration is 60 minutes ± 15 minutes, with the first infusion lasting no less than 60 minutes.
Andre navne:
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Objective Response Rate (ORR)
Tidsramme: 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.
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Progression-Free Survival (PFS)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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
Tidsramme: 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
|
Samarbejdspartnere og efterforskere
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- EC-2026-0002
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
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