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Becotatug Vedotin Plus Cisplatin and Radiotherapy in LA-ESCC
6 juli 2026 bijgewerkt door: Jun wang, Hebei Medical University Fourth Hospital
A Phase Ib, Open-Label, Single-Arm Study of Becotatug Vedotin Combined With Cisplatin and Concurrent Radiotherapy for Locally Advanced Esophageal Squamous Cell Carcinoma
This study is a prospective, single-arm, single-center Phase Ib clinical trial of Becotatug Vedotin in combination with cisplatin and concurrent radiotherapy for locally advanced esophageal squamous cell carcinoma.
The primary objectives are to investigate the maximum tolerated dose (MTD), dose-limiting toxicity (DLT), and recommended Phase II dose (RP2D) of Becotatug Vedotin in combination with cisplatin and concurrent radiotherapy for locally advanced esophageal squamous cell carcinoma.
The secondary objectives are to assess the efficacy and safety of this combination regimen.
Studie Overzicht
Toestand
Nog niet aan het werven
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
This study is a prospective, open-label, single-center, dose-escalation Phase I clinical trial.
During the dose-escalation phase, the classic "3+3" design will be used to guide dose escalation in order to determine the maximum tolerated dose (MTD) and recommended Phase II dose (RP2D).
Eligible subjects who meet the inclusion and exclusion criteria will receive two cycles of Becotatug Vedotin in combination with cisplatin and concurrent radiotherapy, followed by subsequent systemic therapy per the investigator's discretion.
The dose levels of Becotatug Vedotin are 1.5 mg/kg, 2.0 mg/kg, and 2.3 mg/kg (D1,IV,Q3W).
Cisplatin is administered at a dose of 75 mg/m² (D1,IV,Q3W).
The total radiotherapy dose is 50.4
Gy, delivered in 28 fractions of 1.8 Gy each.
Dose-limiting toxicities (DLTs) will be observed during the treatment period until the completion of the entire concurrent chemoradiotherapy phase.
Studietype
Ingrijpend
Inschrijving (Geschat)
12
Fase
- Fase 1
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studiecontact
- Naam: YunJie Cheng
- Telefoonnummer: +8613633115261
- E-mail: jiekejaker@sina.com
Studie Locaties
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Hebei
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Shijiazhuang, Hebei, China, 050000
- The Fourth Hospital of Hebei Medical University
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Contact:
- Jun Wang
- Telefoonnummer: 0311-86095794
- E-mail: wangjunzr@163.com
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Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Nee
Beschrijving
Inclusion Criteria:
- Subjects who are able to understand and voluntarily sign informed consent forms (ICFs).
- Male and female subjects at the age of ≥18 and ≤75 at the time of screening.
- Histologically confirmed esophageal squamous cell carcinoma staged as cT2-T4a, N0-N+, M0-M1 (M1 limited to supraclavicular lymph node metastasis only).
- Patients must have at least one measurable lesion as defined by RECIST version 1.1 criteria.
- Patients who have not received any prior anti-tumor treatment for esophageal cancer.
- ECOG score of 0 or 1.
- Life expectancy ≥ 3 months.
Adequate organ function (no blood transfusion and no use of granulocyte colony-stimulating factor, or other hematopoietic stimulator support within 2 weeks before the first administration of the study drug) confirmed as evidenced by:
- Absolute Neutrophil Count (ANC) ≥ 1.5×10^9/L;
- Hemoglobin (Hgb) ≥ 90 g/dl;
- Platelets (Plt) ≥ 75×10^9/L;
- Bilirubin total ≤ 1.5 x ULN, or bilirubin direct < ULN for patients with bilirubin total levels >1.5 ULN;
- AST/ALT ≤ 2.5 x ULN or ≤ 5.0 x ULN if liver metastases are present;
- Serum creatinine < 1.5 x ULN or creatinine clearance > 50 mL/min (as calculated via Cockcroft-Gault formula based on the actual body weight of the subject ;
- Female subjects must not be pregnant or breastfeeding. Female or male subjects of childbearing potential must agree to practice effective contraceptive measures throughout the study period and for 6 months after completion of study treatment.
Exclusion Criteria:
- Diagnosis of any other malignancy within the past 5 years (excluding carcinoma in situ, basal cell carcinoma, etc.).
- Anyone allergic to any drug or any of its components in this regimen.
- Patients with a prior history of surgery for esophageal squamous cell carcinoma.
- Patients with a prior history of fistula caused by primary tumor infiltration.
- Patients at high risk of gastrointestinal bleeding, esophageal fistula, or esophageal perforation.
- Subjects with poor nutritional status, defined as BMI < 18.5 kg/m² or PG-SGA score ≥ 9.
- Patients with a diagnosis of pulmonary fibrosis or interstitial pneumonia within 28 days prior to enrollment.
- Active infections such as HIV; active chronic HBV/HCV (e.g., HBV DNA ≥ 10⁴ copies/mL or ≥ 2000 IU/mL) requiring antiviral and hepatoprotective therapy before enrollment. Enrollment is allowed only when HBV DNA decreases to < 10⁴ copies/mL or < 2000 IU/mL, with continued antiviral therapy and regular monitoring of liver function and HBV DNA levels.
Presence of major cardiovascular disease, including any of the following conditions:
- Congestive heart failure (defined as New York Heart Association [NYHA] Class III or IV), myocardial infarction, unstable angina, coronary angioplasty, stent implantation, coronary artery bypass grafting, cerebrovascular accident (CVA), or hypertensive crisis within 6 months prior to enrollment.
- History of clinically significant ventricular arrhythmias (e.g., sustained ventricular tachycardia, ventricular fibrillation, torsade de pointes).
- Fridericia-corrected QT interval (QTcF) > 450 msec in males or > 470 msec in females.
- History or family history of congenital long QT syndrome.
- Arrhythmias requiring antiarrhythmic therapy (subjects with atrial fibrillation that has been controlled for more than 30 days prior to randomization may be enrolled).
- History of deep vein thrombosis, pulmonary embolism, or any other serious thromboembolic event within 3 months prior to enrollment (thrombosis related to an implanted venous access port or catheter, or superficial venous thrombosis, is not considered "serious" thromboembolism).
- Severe chronic diarrhea.
- Severe psychiatric disorder.
- Use of strong inhibitors or inducers of CYP3A4, CYP2C8, and UGT1A1.
- Participation in another clinical trial within 4 weeks prior to enrollment.
- Patients who, in the opinion of the investigator, are unsuitable for participation in this study.
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: NVT
- Interventioneel model: Opdracht voor een enkele groep
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
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Experimenteel: Becotatug vedotin + Cisplatin + Radiotherapy
Participants receive Becotatug vedotin (MRG003) in combination with Cisplatin and concurrent radiotherapy.
During the dose-escalation phase, the classic "3+3" design will be used to guide dose escalation in order to determine the maximum tolerated dose (MTD) and recommended Phase II dose (RP2D).
Eligible subjects who meet the inclusion and exclusion criteria will receive two cycles of Becotatug Vedotin in combination with cisplatin and concurrent radiotherapy, followed by subsequent systemic therapy per the investigator's discretion.
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Maximum Tolerated Dose (MTD)
Tijdsspanne: Cycle 1 (21 days)
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MTD is defined as the highest dose level at which DLT is observed in ≤ 1/6 subjects at one single dose group
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Cycle 1 (21 days)
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Recommended Phase 2 Dose (RP2D)
Tijdsspanne: Cycle 1 (21 days)
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RP2D will be a dose either below or equal to MTD
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Cycle 1 (21 days)
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Dose Limiting Toxicity (DLT)
Tijdsspanne: Cycle 1 (21 days)
|
DLT will be evaluated according to NCI-CTCAE V5.0 criteria
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Cycle 1 (21 days)
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Objective response rate(ORR)
Tijdsspanne: From first treatment date until disease progression or death, assessed every 6 weeks, up to approximately 36 months
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Objective response rate (ORR) is the proportion of subjects with the best overall response being CR or PR (assessed by investigator per RECIST v1.1)
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From first treatment date until disease progression or death, assessed every 6 weeks, up to approximately 36 months
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Disease Control Rate (DCR)
Tijdsspanne: From first treatment date until disease progression or death, assessed every 6 weeks, up to approximately 36 months
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Disease Control Rate (DCR) is defined as the proportion of patients who achieve a best overall response of Complete Response (CR), Partial Response (PR), or Stable Disease (SD) according to RECIST 1.1 criteria, among the total number of evaluable patients.
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From first treatment date until disease progression or death, assessed every 6 weeks, up to approximately 36 months
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Progression free survival (PFS)
Tijdsspanne: From first treatment date to disease progression or death, up to 36 months
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Progression-Free Survival (PFS) is defined as the time from randomization (or first dose of study treatment) to the first documented disease progression per RECIST 1.1 criteria, or death from any cause, whichever occurs first.
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From first treatment date to disease progression or death, up to 36 months
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2-year overall survival (OS) rate
Tijdsspanne: From first treatment date to death from any cause, assessed up to 36 months
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The 2-year overall survival (OS) rate is defined as the percentage of patients who remain alive at 2 years after the start of study treatment.
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From first treatment date to death from any cause, assessed up to 36 months
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Incidence and severity of adverse events (AEs)
Tijdsspanne: From first dose date through study completion, up to 36 months
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severity determined according to National Cancer Institute Common Terminology Criteria for Adverse Events [NCI CTCAE] Version [v] 5.0
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From first dose date through study completion, up to 36 months
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Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Geschat)
1 juli 2026
Primaire voltooiing (Geschat)
1 juli 2029
Studie voltooiing (Geschat)
31 december 2029
Studieregistratiedata
Eerst ingediend
20 juni 2026
Eerst ingediend dat voldeed aan de QC-criteria
6 juli 2026
Eerst geplaatst (Werkelijk)
10 juli 2026
Updates van studierecords
Laatste update geplaatst (Werkelijk)
10 juli 2026
Laatste update ingediend die voldeed aan QC-criteria
6 juli 2026
Laatst geverifieerd
1 juni 2026
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
- Neoplasmata per site
- Neoplasmata
- Neoplasmata per histologisch type
- Gastro-intestinale neoplasmata
- Neoplasmata van het spijsverteringsstelsel
- Ziekten van het spijsverteringsstelsel
- Gastro-intestinale aandoeningen
- Hoofd- en nekneoplasmata
- Neoplasmata, glandulair en epitheel
- Slokdarmaandoeningen
- Carcinoom
- Neoplasmata, plaveiselcel
- Carcinoom, plaveiselcel
- Slokdarmneoplasmata
- Slokdarm plaveiselcelcarcinoom
- Anorganische chemicaliën
- Chloorverbindingen
- Stikstofverbindingen
- Platinumverbindingen
- Cisplatine
Andere studie-ID-nummers
- MRG003-LA-ESCC-013
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
NEE
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Nee
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Nee
product vervaardigd in en geëxporteerd uit de V.S.
Nee
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .