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- Klinische proef NCT07656766
Sintilimab Plus Gossypol Acetate in Advanced Colorectal Cancer
22 juni 2026 bijgewerkt door: 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.
Studie Overzicht
Toestand
Nog niet aan het werven
Conditie
Interventie / Behandeling
Studietype
Ingrijpend
Inschrijving (Geschat)
32
Fase
- Fase 2
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: Ziwei Zhang
- Telefoonnummer: +86 18883886902
- E-mail: 786327832@qq.com
Studie Locaties
-
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Beijing Municipality
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Beijing, Beijing Municipality, China, 100044
- Peking University People's Hospital
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Contact:
- Peking University People's Hospital
- Telefoonnummer: +86 18883886902
- E-mail: shenzhanlong@pkuph.edu.cn
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Hoofdonderzoeker:
- Zhanlong Shen, M.D.
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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:
- Written informed consent provided before any study-specific procedures.
- Age 18 to 75 years, male or female.
- Histologically or cytologically confirmed advanced colorectal adenocarcinoma.
- Confirmed pMMR/MSS tumor status. Participants without documented MSI/MMR status must undergo MSI or MMR testing during screening.
- Disease progression after at least two prior lines of standard therapy.
- Availability of tumor tissue suitable for pathological evaluation and biomarker analysis.
- ECOG performance status of 0 or 1 within 7 days before the first dose of study treatment.
- At least one measurable lesion according to RECIST version 1.1.
- Adequate hematologic, hepatic, renal, coagulation, and organ function as defined in the protocol.
- 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:
- Histology of small cell carcinoma, squamous cell carcinoma, or mixed carcinoma.
- dMMR/MSI-H tumor status.
- Complete bowel obstruction or clinical conditions likely to progress to bowel obstruction.
- Suspected bowel perforation based on clinical symptoms or imaging.
- 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.
- Active autoimmune disease, history of autoimmune disease, or immunodeficiency requiring systemic treatment, except protocol-allowed conditions.
- 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.
- History of idiopathic pulmonary fibrosis, organizing pneumonia, drug-induced pneumonitis, idiopathic pneumonitis, or evidence of active pneumonitis on screening chest CT.
- Severe chronic or active infection within 4 weeks before initiation of study treatment.
- Active tuberculosis infection or inadequately treated prior active tuberculosis.
- Active hepatitis B or hepatitis C infection as defined by protocol criteria.
- Uncontrolled tumor-related pain, uncontrolled pleural effusion, pericardial effusion, or ascites requiring frequent drainage.
- History of leptomeningeal disease.
- 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.
- Treatment with systemic immunostimulatory agents within 4 weeks or 5 half-lives before initiation of study treatment, whichever is longer.
- Treatment with systemic immunosuppressive medications within 2 weeks before initiation of study treatment, except protocol-allowed medications.
- Prior allogeneic stem cell transplantation or solid organ transplantation.
- 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.
- 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.
- Receipt of any other investigational drug within 28 days before initiation of study treatment.
- Known contraindication, hypersensitivity, or severe allergic reaction to any study drug or its excipients.
- Pregnancy, breastfeeding, or intention to become pregnant during the study or within 5 months after the last dose of sintilimab.
- 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.
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: Experimental: Sintilimab Plus Gossypol Acetate
Participants will receive oral gossypol acetate and intravenous sintilimab according to the study protocol.
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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.
Andere namen:
Gossypol acetate 20 mg will be administered orally once daily after dinner for 9 weeks, according to the study protocol.
Andere namen:
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Objective Response Rate
Tijdsspanne: At Week 11 after initiation of study treatment
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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.
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At Week 11 after initiation of study treatment
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Disease Control Rate
Tijdsspanne: 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.
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At Week 11 after initiation of study treatment
|
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Progression-Free Survival
Tijdsspanne: From the first dose of study treatment up to 24 months
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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.
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From the first dose of study treatment up to 24 months
|
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Overall Survival
Tijdsspanne: 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.
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From the first dose of study treatment up to 24 months
|
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Duration of Response
Tijdsspanne: From the first documented response up to 24 months
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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.
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From the first documented response up to 24 months
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Adverse events (AEs) were graded according to the NCI CTCAE version 5.0
Tijdsspanne: From the first dose of study treatment through 30 days after the last dose of study treatment
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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.
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From the first dose of study treatment through 30 days after the last dose of study treatment
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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)
15 juli 2026
Primaire voltooiing (Geschat)
15 september 2027
Studie voltooiing (Geschat)
15 september 2029
Studieregistratiedata
Eerst ingediend
15 juni 2026
Eerst ingediend dat voldeed aan de QC-criteria
15 juni 2026
Eerst geplaatst (Werkelijk)
18 juni 2026
Updates van studierecords
Laatste update geplaatst (Werkelijk)
25 juni 2026
Laatste update ingediend die voldeed aan QC-criteria
22 juni 2026
Laatst geverifieerd
1 juni 2026
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
- Neoplasmata per site
- Neoplasmata
- Darmziekten
- Gastro-intestinale neoplasmata
- Neoplasmata van het spijsverteringsstelsel
- Ziekten van het spijsverteringsstelsel
- Gastro-intestinale aandoeningen
- Intestinale neoplasmata
- Rectale ziekten
- Colon Ziekten
- Colorectale neoplasmata
- Antineoplastische middelen, immunologisch
- Antineoplastische middelen
- Moleculaire mechanismen van farmacologische werking
- Organische chemicaliën
- Farmacologische acties
- Chemische acties en gebruik
- Therapeutisch gebruik
- Koolwaterstoffen
- Terpenen
- Sesquiterpenes
- Immuun Checkpoint-remmers
- Sintilimab
- Gossypol
Andere studie-ID-nummers
- 2025PHD051-001
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
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 .