Sintilimab Plus Gossypol Acetate in Advanced Colorectal Cancer
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
Studieoversigt
Status
Status
Betingelser
Betingelser
Intervention / Behandling
Intervention / Behandling
Undersøgelsestype
Undersøgelsestype
Tilmelding (Anslået)
Tilmelding
Fase
Fase
- Fase 2
Kontakter og lokationer
Studiekontakt
Studiekontakt
- Navn: Ziwei Zhang
- Telefonnummer: +86 18883886902
- E-mail: 786327832@qq.com
Studiesteder
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Beijing Municipality
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Beijing, Beijing Municipality, Kina, 100044
- Peking University People's Hospital
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Kontakt:
- Peking University People's Hospital
- Telefonnummer: +86 18883886902
- E-mail: shenzhanlong@pkuph.edu.cn
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Ledende efterforsker:
- Zhanlong Shen, M.D.
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Deltagelseskriterier
Berettigelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
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.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Antal våben
Våben og indgreb
Deltagergruppe / ArmDeltagergruppe / Arm |
Intervention / BehandlingIntervention / Behandling |
|---|---|
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Eksperimentel: 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.
Andre navne:
Gossypol acetate 20 mg will be administered orally once daily after dinner for 9 weeks, according to the study protocol.
Andre navne:
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Hvad måler undersøgelsen?
Primære resultatmål
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Objective Response Rate
Tidsramme: 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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Sekundære resultatmål
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Disease Control Rate
Tidsramme: At Week 11 after initiation of study treatment
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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
Tidsramme: 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
Tidsramme: From the first dose of study treatment up to 24 months
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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
Tidsramme: 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
Tidsramme: 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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Samarbejdspartnere og efterforskere
Sponsor
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Studiestart
Primær færdiggørelse (Anslået)
Primær færdiggørelse
Studieafslutning (Anslået)
Studieafslutning
Datoer for studieregistrering
Først indsendt
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Først opslået
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering sendt
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
- Neoplasmer efter sted
- Neoplasmer
- Tarmsygdomme
- Gastrointestinale neoplasmer
- Neoplasmer i fordøjelsessystemet
- Sygdomme i fordøjelsessystemet
- Gastrointestinale sygdomme
- Intestinale neoplasmer
- Endetarmssygdomme
- Tyktarmssygdomme
- Kolorektale neoplasmer
- Antineoplastiske midler, immunologiske
- Antineoplastiske midler
- Molekylære mekanismer for farmakologisk virkning
- Organiske kemikalier
- Farmakologiske handlinger
- Kemiske handlinger og anvendelser
- Terapeutiske anvendelser
- Kulbrinter
- Terpenes
- Sesquiterpenes
- Immune Checkpoint-hæmmere
- SINTILIMAB
- Gossypol
Andre undersøgelses-id-numre
Andre undersøgelses-id-numre
- 2025PHD051-001
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
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