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Recruiting nowPhase 1/2Ages 18 Years to 70 Years

Triplex Checkpoint Inhibitors Therapy for Advanced Solid Tumors

Sponsor: Second Affiliated Hospital of Guangzhou Medical University · NCT05187338 on ClinicalTrials.gov ↗

Conditions studied

Lung CancerLiver CancerColorectal CancerPancreas CancerOvary CancerHead and Neck CancerBreast CancerGastric CancerCervical CancerEsophageal CancerSarcoma

What it tests

  • ipilimumab +pembrolizumab +durvalumabdrug

Where it's running1 site

1 international site
  • The Second Affiliated Hospital of Guangzhou Medical University

    Guangzhou, Guangdong, China 510260

    Recruiting now
    • Zhenfeng Zhang, MD, PHD(contact)
    • Bingjia He, MD(contact)
See the official eligibility language

Shown exactly as written on ClinicalTrials.gov. Your oncologist is the right person to judge whether it fits your situation.

Inclusion Criteria:

1. Cytohistological confirmation is required for diagnosis of cancer.
2. Signed informed consent before recruiting.
3. Age above 18 years with estimated survival over 3 months.
4. Child-Pugh class A or B/Child score \> 7; ECOG score \< 2
5. Tolerable coagulation function or reversible coagulation disorders
6. Laboratory examination test within 7 days prior to procedure: WBC≥3.0×10E9/L; Hb≥90g/L; PLT ≥50×10E9/L;INR \< 2.3 or PT \< 6 seconds above control;Cr ≤ 145.5 umul/L;Albumin \> 28 g/L;Total bilirubin \< 51 μmol/L
7. At least one tumor lesion meeting measurable disease criteria as determined by RECIST v1.1.
8. Birth control.
9. Willing and able to comply with scheduled visits, treatment plan and laboratory tests.

Exclusion Criteria:

1. Patients participated in clinical trials of equipment or drugs (signed informed consent) within 4 weeks;
2. Patients accompany by ascites, hepatic encephalopathy and esophageal and gastric varices bleeding;
3. Any serious accompanying disease, which is expected to have an unknown, impact on the prognosis, include heart disease, inadequately controlled diabetes and psychiatric disorders;
4. Patients accompanied with other tumors or past medical history of malignancy;
5. Pregnant or lactating patients, all patients participating in this trial must adopt appropriate birth control measures during treatment;
6. Patients have poor compliance.

   Any contraindications for hepatic arterial infusion procedure:

   A.Impaired clotting test (platelet count \< 60000/mm3, prothrombin activity \< 50%).

   B.Renal failure / insufficiency requiring hemo-or peritoneal dialysis. C.Known severe atheromatosis. D.Known uncontrolled blood hypertension (\> 160/100 mm/Hg).
7. Allergic to contrast agent;
8. Any agents which could affect the absorption or pharmacokinetics of the study drugs
9. Other conditions that investigator decides not suitable for the trial.

Updated 2024-06-25 on ClinicalTrials.gov. Always confirm current details with the study team or your oncologist.