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Sintilimab Plus Gossypol Acetate in Advanced Colorectal Cancer

22 juin 2026 mis à jour par: Shen Zhanlong, Peking University People's Hospital

A Single-Arm, Open-Label, Exploratory Phase II Clinical Trial of Sintilimab Plus Gossypol Acetate in Patients With Advanced pMMR/MSS Colorectal Cancer After Failure of at Least Two Prior Lines of Therapy

This is a single-center, open-label, single-arm, exploratory phase II clinical trial designed to evaluate the preliminary efficacy and safety of sintilimab in combination with oral gossypol acetate in patients with advanced pMMR/MSS colorectal cancer after failure of at least two prior lines of standard therapy. Eligible participants will have histologically or cytologically confirmed advanced colorectal adenocarcinoma, measurable disease according to RECIST version 1.1, ECOG performance status of 0 or 1, and adequate organ function. Participants will receive oral gossypol acetate once daily, followed by sintilimab administered intravenously every 3 weeks after a gossypol acetate lead-in period. The primary outcome is objective response rate assessed by RECIST version 1.1. Secondary outcomes include disease control rate, progression-free survival, overall survival, duration of response, and safety.

Aperçu de l'étude

Statut

Pas encore de recrutement

Les conditions

Type d'étude

Interventionnel

Inscription (Estimé)

32

Phase

  • Phase 2

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

  • Nom: Ziwei Zhang
  • Numéro de téléphone: +86 18883886902
  • E-mail: 786327832@qq.com

Lieux d'étude

    • Beijing Municipality
      • Beijing, Beijing Municipality, Chine, 100044
        • Peking University People's Hospital
        • Contact:
        • Chercheur principal:
          • Zhanlong Shen, M.D.

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Non

La description

Inclusion Criteria:

  1. Written informed consent provided before any study-specific procedures.
  2. Age 18 to 75 years, male or female.
  3. Histologically or cytologically confirmed advanced colorectal adenocarcinoma.
  4. Confirmed pMMR/MSS tumor status. Participants without documented MSI/MMR status must undergo MSI or MMR testing during screening.
  5. Disease progression after at least two prior lines of standard therapy.
  6. Availability of tumor tissue suitable for pathological evaluation and biomarker analysis.
  7. ECOG performance status of 0 or 1 within 7 days before the first dose of study treatment.
  8. At least one measurable lesion according to RECIST version 1.1.
  9. Adequate hematologic, hepatic, renal, coagulation, and organ function as defined in the protocol.
  10. Female participants of childbearing potential must have a negative pregnancy test before initiation of study treatment and agree to use effective contraception during the study and for the protocol-specified period after the last dose.

Exclusion Criteria:

  1. Histology of small cell carcinoma, squamous cell carcinoma, or mixed carcinoma.
  2. dMMR/MSI-H tumor status.
  3. Complete bowel obstruction or clinical conditions likely to progress to bowel obstruction.
  4. Suspected bowel perforation based on clinical symptoms or imaging.
  5. History of malignancy other than colorectal cancer within 3 years before screening, except malignancies with negligible risk of metastasis or death and treated with expected curative outcome.
  6. Active autoimmune disease, history of autoimmune disease, or immunodeficiency requiring systemic treatment, except protocol-allowed conditions.
  7. Significant cardiovascular disease within 3 months before initiation of study treatment, including New York Heart Association class II or higher heart disease, myocardial infarction, cerebrovascular accident, unstable arrhythmia, or unstable angina.
  8. History of idiopathic pulmonary fibrosis, organizing pneumonia, drug-induced pneumonitis, idiopathic pneumonitis, or evidence of active pneumonitis on screening chest CT.
  9. Severe chronic or active infection within 4 weeks before initiation of study treatment.
  10. Active tuberculosis infection or inadequately treated prior active tuberculosis.
  11. Active hepatitis B or hepatitis C infection as defined by protocol criteria.
  12. Uncontrolled tumor-related pain, uncontrolled pleural effusion, pericardial effusion, or ascites requiring frequent drainage.
  13. History of leptomeningeal disease.
  14. Prior treatment with CD137 agonists, T-cell co-stimulatory agents, or immune checkpoint inhibitors, including anti-CTLA-4, anti-PD-1, anti-PD-L1, or anti-TIGIT antibodies.
  15. Treatment with systemic immunostimulatory agents within 4 weeks or 5 half-lives before initiation of study treatment, whichever is longer.
  16. Treatment with systemic immunosuppressive medications within 2 weeks before initiation of study treatment, except protocol-allowed medications.
  17. Prior allogeneic stem cell transplantation or solid organ transplantation.
  18. Receipt of a live attenuated vaccine within 4 weeks before initiation of study treatment or expected need for such vaccination during the study or within 5 months after the last dose of sintilimab.
  19. Major surgery or severe traumatic injury within 28 days before initiation of study treatment, abdominal surgery or abdominal intervention within 60 days before initiation of study treatment, or expected need for major surgery during the study.
  20. Receipt of any other investigational drug within 28 days before initiation of study treatment.
  21. Known contraindication, hypersensitivity, or severe allergic reaction to any study drug or its excipients.
  22. Pregnancy, breastfeeding, or intention to become pregnant during the study or within 5 months after the last dose of sintilimab.
  23. Any other disease, laboratory abnormality, social condition, or medical condition that, in the investigator's judgment, may compromise participant safety, interfere with study compliance, or affect interpretation of study results.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: N / A
  • Modèle interventionnel: Affectation à un seul groupe
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Experimental: Sintilimab Plus Gossypol Acetate
Participants will receive oral gossypol acetate and intravenous sintilimab according to the study protocol.
Sintilimab 200 mg will be administered intravenously every 3 weeks for 3 cycles after a gossypol acetate lead-in period, according to the study protocol.
Autres noms:
  • IBI308
  • Inhibiteur PD-1
Gossypol acetate 20 mg will be administered orally once daily after dinner for 9 weeks, according to the study protocol.
Autres noms:
  • Compound Gossypol Acetate Tablet

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Objective Response Rate
Délai: At Week 11 after initiation of study treatment
Objective response rate is defined as the proportion of participants who achieve complete response or partial response as their best overall response, as assessed according to RECIST version 1.1 by independent radiologic review.
At Week 11 after initiation of study treatment

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Disease Control Rate
Délai: At Week 11 after initiation of study treatment
Disease control rate is defined as the proportion of participants who achieve complete response, partial response, or stable disease as their best overall response according to RECIST version 1.1.
At Week 11 after initiation of study treatment
Progression-Free Survival
Délai: From the first dose of study treatment up to 24 months
Progression-free survival is defined as the time from the first dose of study treatment to the first documented disease progression according to RECIST version 1.1 or death from any cause, whichever occurs first.
From the first dose of study treatment up to 24 months
Overall Survival
Délai: From the first dose of study treatment up to 24 months
Overall survival is defined as the time from the first dose of study treatment to death from any cause.
From the first dose of study treatment up to 24 months
Duration of Response
Délai: From the first documented response up to 24 months
Duration of response is defined as the time from the first documented complete response or partial response to disease progression or death from any cause, whichever occurs first.
From the first documented response up to 24 months
Adverse events (AEs) were graded according to the NCI CTCAE version 5.0
Délai: From the first dose of study treatment through 30 days after the last dose of study treatment
Adverse events, serious adverse events, treatment-related adverse events, and immune-related adverse events will be assessed and graded according to NCI CTCAE version 5.0.
From the first dose of study treatment through 30 days after the last dose of study treatment

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

15 juillet 2026

Achèvement primaire (Estimé)

15 septembre 2027

Achèvement de l'étude (Estimé)

15 septembre 2029

Dates d'inscription aux études

Première soumission

15 juin 2026

Première soumission répondant aux critères de contrôle qualité

15 juin 2026

Première publication (Réel)

18 juin 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

25 juin 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

22 juin 2026

Dernière vérification

1 juin 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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