- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT07656766
Sintilimab Plus Gossypol Acetate in Advanced Colorectal Cancer
22 juni 2026 uppdaterad av: 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.
Studieöversikt
Status
Har inte rekryterat ännu
Betingelser
Intervention / Behandling
Studietyp
Interventionell
Inskrivning (Beräknad)
32
Fas
- Fas 2
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studiekontakt
- Namn: Ziwei Zhang
- Telefonnummer: +86 18883886902
- E-post: 786327832@qq.com
Studieorter
-
-
Beijing Municipality
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Beijing, Beijing Municipality, Kina, 100044
- Peking University People's Hospital
-
Kontakt:
- Peking University People's Hospital
- Telefonnummer: +86 18883886902
- E-post: shenzhanlong@pkuph.edu.cn
-
Huvudutredare:
- Zhanlong Shen, M.D.
-
-
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
- Vuxen
- Äldre vuxen
Tar emot friska volontärer
Nej
Beskrivning
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
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: N/A
- Interventionsmodell: Enskild gruppuppgift
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
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Experimentell: 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.
Andra namn:
Gossypol acetate 20 mg will be administered orally once daily after dinner for 9 weeks, according to the study protocol.
Andra namn:
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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Objective Response Rate
Tidsram: 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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Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Disease Control Rate
Tidsram: 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
|
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Progression-Free Survival
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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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Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart (Beräknad)
15 juli 2026
Primärt slutförande (Beräknad)
15 september 2027
Avslutad studie (Beräknad)
15 september 2029
Studieregistreringsdatum
Först inskickad
15 juni 2026
Först inskickad som uppfyllde QC-kriterierna
15 juni 2026
Första postat (Faktisk)
18 juni 2026
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
25 juni 2026
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
22 juni 2026
Senast verifierad
1 juni 2026
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
- Neoplasmer efter plats
- Neoplasmer
- Tarmsjukdomar
- Gastrointestinala neoplasmer
- Neoplasmer i matsmältningssystemet
- Matsmältningssystemets sjukdomar
- Gastrointestinala sjukdomar
- Intestinala neoplasmer
- Rektala sjukdomar
- Kolonsjukdomar
- Kolorektala neoplasmer
- Antineoplastiska medel, immunologiska
- Antineoplastiska medel
- Molekylära mekanismer för farmakologisk verkan
- Organiska kemikalier
- Farmakologiska åtgärder
- Kemiska åtgärder och användningar
- Terapeutisk användning
- Kolväten
- Terpener
- Sesquiterpenes
- Immune Checkpoint-hämmare
- sintilimab
- Gossypol
Andra studie-ID-nummer
- 2025PHD051-001
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
NEJ
Läkemedels- och apparatinformation, studiedokument
Studerar en amerikansk FDA-reglerad läkemedelsprodukt
Nej
Studerar en amerikansk FDA-reglerad produktprodukt
Nej
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .