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A Randomized, Controlled, Double-Blind, Multicenter Phase III Clinical Trial to Evaluate the Efficacy and Safety of Enlonstobart, With or Without SYS6010 as Adjuvant Therapy, in Participants With Pathologically Residual Esophageal Squamous Cell Carcinoma Following Complete Surgical Resection

2. november 2026 opdateret af: CSPC Megalith Biopharmaceutical Co.,Ltd.

This is a randomized, controlled, double-blind, multicenter phase iii clinical trial to evaluate the efficacy and safety of enlonstobart, with or without SYS6010 as adjuvant therapy, in participants with pathologically residual esophageal squamous cell carcinoma following complete surgical resection.

Studieoversigt

Detaljeret beskrivelse

This study is a randomized, double-blind, three-arm, placebo-controlled, multicenter Phase III trial designed to evaluate the efficacy and safety of SG001, with or without SYS6010, compared to placebo as adjuvant therapy following radical surgery with R0 resection but with pathological residual disease (ypT1-4aN0M0 or ypT0-4aN+M0) in patients with resectable Stage II -III esophageal squamous cell carcinoma who achieved R0 resection following curative surgery after neoadjuvant therap.

The study plans to enroll 585 participants who have previously undergone curative surgery for esophageal cancer, with R0 resection at surgery, pathologically confirmed failure to achieve pCR, and who have signed an informed consent form. Participants will be randomly assigned in a 2:2:1 ratio to the following groups in a double-blind manner: SG001 + SYS6010 vs. SG001 + placebo-mimicking SYS6010 vs. SG001 placebo-mimicking + placebo-mimicking SYS6010.

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

585

Fase

  • Fase 3

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

  • Navn: Clinical Trials Information Group officer
  • Telefonnummer: 031169085587
  • E-mail: ctr-contact@cspc.cn

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  1. Be able to understand and voluntarily sign the written ICF;

  2. Age over 18 years, male or female;

  3. With histologically/cytologically confirmed esophageal squamous cell carcinoma that is clinically staged as stage II-III , neoadjuvant therapy must be completed prior to randomization, followed by curative surgery for esophageal squamous cell carcinoma, and all of the following criteria must be met:

    Neoadjuvant therapy includes: at least 2 cycles of platinum-based chemotherapy (± immune checkpoint inhibitors) or chemoradiotherapy, with no clinically or radiologically confirmed disease progression during the neoadjuvant therapy phase.

    Participants must have achieved R0 complete resection, with the surgery resulting in a tumor-free state and negative surgical margins.

    Prior to randomization, the Center's Independent Pathology Review Committee (CPIRC) will evaluate the participant's postoperative pathology report (pathology report must be provided). Participants who do not achieve pathological complete response (non-pCR) and have pathological residual disease (ypT1-4aN0M0 or ypT0-4aN+M0) will have their pathology results assessed and confirmed by the Center's Independent Pathology Review Committee in cases of uncertain pathology (e.g., ypNx).

    Postoperative adjuvant therapy must begin 4-16 weeks after curative surgery.;

  4. Eastern Cooperative Oncology Group (ECOG) performance status score: 0-1;

  5. Life expectancy ≥ 3 months;

Exclusion Criteria:

  1. Pathologically diagnosed esophageal carcinoma, including adenocarcinoma, adenosquamous carcinoma, or other histological subtypes;
  2. Previous treatment with irinotecan-based agents or topoisomerase I inhibitor-based toxin-conjugated antibody (ADC) drugs; For patients who have received treatment with immune checkpoint inhibitors (e.g., anti-PD-1/PD-L1 monoclonal antibodies) during the neoadjuvant phase: a history of Grade ≥3 immune-related adverse events (irAEs), or a history of irAEs leading to permanent discontinuation of immunotherapy, or a history of immune-related interstitial pneumonia, myocarditis, encephalitis, or severe neurological toxicity of any grade;
  3. Patients who have received other anticancer therapies following curative surgery for esophageal squamous cell carcinoma, including chemotherapy, targeted therapy, radiation therapy, biologic therapy, immunotherapy, or treatment with traditional Chinese medicine products approved for such indications; Patients with a known allergy to any component of the SYS6010 product or to humanized monoclonal antibody products;
  4. BMI < 16.0 kg/m² or body weight < 40 kg;

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Firedobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: SG001 + SYS6010

SYS6010 is an antibody conjugate drug (ADC), composed of one anti-EGFR monoclonal antibody coupled to one JS1 via an enzyme specific linker.

SG001 is a recombinant, fully human, anti-PD-1 monoclonal antibody.

Eksperimentel: SG001 + placebo-mimicking SYS6010

SG001 is a recombinant, fully human, anti-PD-1 monoclonal antibody.

SYS6010 placebo-mimicking is a placebo mimicking of SYS6010

Placebo komparator: SG001 placebo-mimicking + placebo-mimicking SYS6010

SYS6010 placebo-mimicking is a placebo mimicking of SYS6010

SG001 placebo-mimicking is a placebo mimicking of SG001

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
DFS
Tidsramme: From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 60 months

Disease Free Surviva Arm1 vs Arm3 Arm2 vs Arm3

From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 60 months

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
OS :Description: Overall survival
Tidsramme: From date of randomization until the date of death from any cause, assessed up to 60 months.

Overall survival

From date of randomization until the date of death from any cause, assessed up to 60 months.
DMFS
Tidsramme: From date of randomization until the date of first documented distant recurrence/distant metastasis or date of death from any cause, whichever came first, assessed up to 60 months.

Distant Metastasis-Free Survival

From date of randomization until the date of first documented distant recurrence/distant metastasis or date of death from any cause, whichever came first, assessed up to 60 months.
Serum concentrations of toxin-bound antibodies for SYS6010
Tidsramme: From first dose of treatment to 30 days after the last dose of treatment.

Serum concentrations of toxin-bound antibodies following single and multiple doses of SYS6010

From first dose of treatment to 30 days after the last dose of treatment.
Plasma concentration of SG001 following single and multiple doses of SG001
Tidsramme: From first dose of treatment to 30 days after the last dose of treatment.

Plasma concentration of SG001 following single and multiple doses of SG001

From first dose of treatment to 30 days after the last dose of treatment.
Quality of life indicators assessed using the EORTC QLQ-C30;
Tidsramme: Evaluated during the screening period (Day -28 to Day 1),during the treatment period (at each tumor assessment), and at the End of Treatment visit.
Evaluated during the screening period (Day -28 to Day 1),during the treatment period (at each tumor assessment), and at the End of Treatment visit.
mmunogenicity: incidence and titers of ADA for SYS6010 and SG001, incidence of neutralizing antibodies (if applicable).
Tidsramme: From first dose of treatment to 30 days after the last dose of treatment.
From first dose of treatment to 30 days after the last dose of treatment.
AE
Tidsramme: From first dose of treatment to 90 days after the last dose of treatment.

Incidence and severity of adverse events

From first dose of treatment to 90 days after the last dose of treatment.
Serum concentrations of total antibodies for SYS6010;
Tidsramme: From first dose of treatment to 30 days after the last dose of treatment.

Serum concentrations of total antibodies following single and multiple doses of SYS6010.

From first dose of treatment to 30 days after the last dose of treatment.
Plasma concentration of SG001 following single and multiple doses of SG001;
Tidsramme: From first dose of treatment to 30 days after the last dose of treatment.

Serum concentrations of JS-1 following single and multiple doses of SYS6010.

From first dose of treatment to 30 days after the last dose of treatment.

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

30. december 2026

Primær færdiggørelse (Anslået)

30. december 2029

Studieafslutning (Anslået)

30. december 2030

Datoer for studieregistrering

Først indsendt

26. oktober 2026

Først indsendt, der opfyldte QC-kriterier

2. november 2026

Først opslået (Faktiske)

9. november 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

9. november 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

2. november 2026

Sidst verificeret

1. november 2026

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