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The Culture of Advanced/Recurrent/Metastatic Colorectal Cancer Organoids and Drug Screening

C

Chongqing University Cancer Hospital

Status

Enrolling

Conditions

Colorectal Cancer

Study type

Observational

Funder types

Other

Identifiers

NCT05304741
CQGOG0501

Details and patient eligibility

About

The study aims to establish an organoids platform and apply them to screen drugs for advanced/recurrent/metastatic colorectal cancer patients.

Full description

The study was designed as a prospective, observational clinical trial in a single center. We establish organoids derived from patients with advanced/recurrent/metastatic colorectal cancer. Organoids will be validated with a combination of Next Generation Sequencing (NGS) analysis and histopathology. Drug screening assay will be performed on organoids with the chemotherapy and targeted agents, and the sensitivity and speciality will be compared with the clinical practice.

Enrollment

30 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients voluntarily participated in the study and signed informed consent;
  2. ECOG score 0~2;
  3. Expected survival over 6 months;
  4. The serum or urine pregnancy test must be negative within 7 days before enrollment for the women of childbearing age who should agree that contraception must be used during the trial;
  5. CBC: Hb≥70g/L、WBC≥3.5×109/ L 、ANC≥1.5×109/L、PLT≥80×109/L;
  6. Serum ALT≤2×UL, AST≤2×ULN; Serum creatinine≤1.5×ULN;
  7. Colorectal cancer was unresectable and confirmed as adenocarcinoma by histopathology. Patients have no significant symptoms in the primary lesion (no bleeding, perforation and obstruction in the primary focus). Besides, the carcinoma is potentially resectable but the patient refuses surgery;
  8. Patients can comply with the research scheme according to the judgment of the researcher.

Exclusion criteria

  1. Activity or uncontrol severe infection;
  2. Liver cirrhosis, Decompensated liver disease;
  3. History of immune deficiency, including HIV positive or suffering from a congenital immunodeficiency disease;
  4. Chronic renal insufficiency or renal failure;
  5. Other malignancies which diagnosed within 5 years or needed to be treated;
  6. Myocardial infarction, severe arrhythmia and NYHA (New York heart association)≥2 for congestive heart failure
  7. Concomitant diseases are treated by drugs that impair liver or kidney function, such as tuberculosis.

Trial contacts and locations

1

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Central trial contact

Dongling Zou

Data sourced from clinicaltrials.gov

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