A Phase 1 interventional study of iNeo-Vac-T01 in Metastatic Colorectal Cancer (CRC), sponsored by Ying Yuan, MD. Recruiting at 1 site in China. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2026-04-01.
Sponsored by Ying Yuan, MD · Phase 1, Interventional, and Treatment
The primary objective of this study is to evaluate the feasibility, safety, and efficacy of personalized T-cell therapy based on tumor neoantigens in patients with advanced colorectal cancer, so as to provide a novel individualized therapeutic strategy for such patients.
5,599 studies on the registry are indexed under Colorectal Neoplasms; 1,459 are open to participants now.
This study's planned enrollment of 20 is below the median of 77 across 4,123 interventional studies indexed under Colorectal Neoplasms.
Browse Colorectal Neoplasms studies →Ying Yuan, MD is the lead sponsor of 2 studies on the registry; 1 is open to participants now.
Counted across the registry records on this site, refreshed daily.
Normal hematological parameters:
Neutrophil count ≥ 1.5 × 10⁹/L Hemoglobin ≥ 10 g/dL Platelet count ≥ 100 × 10⁹/L
Normal biochemical parameters:
Total bilirubin ≤ 1.5 × upper limit of normal (ULN); ≤ 3 × ULN allowed in patients with liver metastasis AST and ALT ≤ 2.5 × ULN; ≤ 5 × ULN allowed in patients with liver metastasis Serum creatinine and blood urea nitrogen (BUN) ≤ 1.5 × ULN
For women of childbearing potential:
negative pregnancy test within 7 days before enrollment, no intention to become pregnant in the near term, and willingness to use effective contraception during the study; Pregnant or lactating women are excluded.
Exclusion Criteria
Concurrent malignancy other than the following:
cured basal cell carcinoma, thyroid cancer, cervical dysplasia, and disease-free for more than 5 years with low risk of recurrence in the investigator's judgment.
Symptomatic or untreated known brain metastasis or other central nervous system (CNS) metastases.
Patients with completely resected and/or irradiated CNS metastases that are stable or improved (radiologically stable for at least 4 weeks prior to randomization by CT/MRI, no evidence of cerebral edema, and no requirement for glucocorticoids or anticonvulsants) are eligible.
Severe asthma, autoimmune disease, or immunodeficiency requiring immunosuppressive therapy.
Excluded: vitiligo, type 1 diabetes, autoimmune hypothyroidism controlled by hormones, psoriasis not requiring systemic therapy.
Uncontrolled comorbidities including but not limited to:
active infection, symptomatic congestive heart failure, unstable angina, cardiac arrhythmia; severe coronary artery disease or cerebrovascular disease; or other conditions deemed ineligible by the investigator.
iNeo-Vac-T01
Biological: iNeo-Vac-T01
iNeo-Vac-T01 Injection is an individually customized tumor neoantigen-specific T cell injection. DNA and RNA sequencing is performed on the tumor tissue of each subject to analyze and predict the tumor neoantigens presented by tumor cells. Meanwhile, the subject's own peripheral blood is collected, and neoantigen-specific T cells are obtained through isolation and culture, then reinfused into the subject. These specific T cells recognize and kill tumor cells expressing the corresponding neoantigens, thereby achieving the goal of inhibiting tumor growth.
Feasibility:Ratio of patients receiving iNeo-Vac-T01 infusion to total enrolled patients
Ratio of patients receiving iNeo-Vac-T01 infusion to total enrolled patients.
Time frame: 36months
Safety and tolerable dose
Number of subjects with adverse events and/or dose-limiting toxicities in accordance with the Common Terminology Criteria for Adverse Events (CTCAE) Version 4.0, which serves as an indicator for evaluating the safety and tolerable dose of iNeo-Vac-T01 injection, with an observation period of approximately 6 months during the dose-escalation phase.
Time frame: 36 months
Overall Response Rate (ORR)
Evaluation of overall response (OR) based on changes in target lesions per RECIST v1.1, including Complete Response (CR, proportion of patients with disappearance of all target lesions) and Partial Response (PR, proportion of patients with a ≥30% reduction in the sum of the longest diameters of target lesions).
Time frame: 36 months
Progression-Free Survival (PFS)
Time from the date of the first iNeo-Vac-T01 injection infusion to the date of disease progression or death due to any cause, with an evaluation period of 3 years.
Time frame: 36 months
Neoantigen-specific T-cell immune response
Detection of the secretion level of specific TNF-γ in peripheral blood of subjects by ELISpot assay, mainly for observing specific T-cell responses, with an evaluation period of 6 months.
Time frame: 6 months
T-cell subset analysis
Proportions of CD8+, CD4+ and other T-cell subsets within T cells, detected by flow cytometry, mainly for assessing the immune status of patients, with an evaluation period of 6 months.
Time frame: 6 months
Cytokines analysis
Changes in interleukin-6 (IL-6), interleukin-10 (IL-10) and tumor necrosis factor-α (TNF-α) in peripheral blood, with an evaluation period of 6 months.
Time frame: 6 months
Plan to share: No
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