Universal CAR-T Cells (REVO-UWD-01) for Metastatic Colorectal Cancer (Wondercel-UWD1)

Wondercel Biotech (ShenZhen)

Status and phase: Enrolling; Early Phase 1

Conditions: Metastatic Colorectal Cancer; CRC (Colorectal Cancer)

Treatments: Biological: Universal CAR-T cells injection for treating mCRC

Study type: Interventional

Funder types: Industry

Identifiers

NCT06653010

2024-REVO-UWD-01

Details and patient eligibility

About

This is an investigator initiated trial to assess the efficacy and safety of a GCC-targeting CAR-T therapy (REVO-UWD-01) in the metastatic colorectal cancer. It also aims to explore the feasibility of using a novel universal CAR-T cell platform.

Full description

The study will use T cells from healthy donors, modified using a novel universal CAR-T technology, to treat metastatic colorectal cancer patients. The antigen-binding site of the CAR molecule recognizes GCC as the target.

The main questions it aims to answer are:

• What is the maximum tolerated dose (MTD) of GCC-CAR-T therapy in universal CAR-T cell treatments?
• What are the dose-limiting toxicities (DLT) and treatment-emergent adverse events (TEAE)?
• What is the treatment's efficacy, as measured by objective response rate (ORR) and progression-free survival (PFS)? Researchers will assess whether universal CAR-T cells have good safety and efficacy in treating colorectal cancer, while improving accessibility and lowering treatment costs.

Participants will:

• Receive universal GCC-CAR-T cells through a 3+3 dose escalation scheme.
• Undergo chemotherapy conditioning before CAR-T infusion.
• Be monitored for adverse events, immune response, and disease progression.

The study will collect data on both short-term outcomes (within the first few months post-treatment) and long-term safety and efficacy.

Enrollment: 30 estimated patients

Sex: All

Ages: 18 to 75 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

1. Age: ≥18 years and ≤75 years old.

2. Pathological Diagnosis: Pathologically confirmed metastatic colorectal cancer with radiographically confirmed metastatic lesions (e.g., CT or MRI).

3. GCC Expression: Tumor lesions assessed by immunohistochemistry (IHC) showing GCC expression ≥1+ in ≥50% of the area (randomly select at least 5 fields from tumor regions for evaluation; at least 5 unstained slides must be provided for assessment).

4. Measurable Lesions: At least one measurable lesion per RECIST 1.1 criteria; measurable lesions should not have received prior radiotherapy or interventional local therapy (lesions in previously irradiated or locally treated fields may be selected as target lesions if confirmed to have progressed).

5. Prior Treatment: Participants with advanced colorectal cancer who have progressed or are intolerant after ≥2 lines of standard therapy (with clear documentation).

6. ECOG Performance Status: 0 or 1.

7. Expected Survival: ≥90 days (as assessed by the investigator based on the participant's clinical condition).

8. Organ Function:

9. Absolute neutrophil count ≥1.5 × 10⁹/L;

10. Platelet count ≥80 × 10⁹/L;

11. Hemoglobin ≥9 g/dL;

12. Liver function:

    1. Total bilirubin ≤1.5 × ULN (≤2.0 × ULN for Gilbert's syndrome);
    2. AST and ALT ≤5 × ULN;

13. INR <1.3 (INR <3 for participants on anticoagulant therapy);

14. Serum creatinine ≤1.5 mg/dL (132.6 μmol/L) or eGFR ≥50 mL/min/1.73 m²;

15. Cardiac ejection fraction >50%.

16. Bleeding Risk: No active bleeding or bleeding tendency.

17. Fertility Requirements:

18. Women of childbearing potential must have a negative pregnancy test (serum or urine) within 7 days prior to enrollment and agree to use effective contraception during treatment and for 8 weeks after the last dose;

19. Male participants must also use effective contraception during treatment and for 8 weeks after the last dose.

20. Informed Consent: Participants voluntarily enroll in the study, provide signed informed consent, demonstrate good compliance, and cooperate with follow-up.

Exclusion Criteria：

1. • Pregnant or breastfeeding women;
2. • Received chemotherapy, targeted therapy, monoclonal antibody therapy, or traditional Chinese medicine anti-tumor therapy within 14 days prior to cell collection;
3. • Participated in another drug clinical trial within 4 weeks prior to study initiation;
4. • Any of the following cardiovascular or cerebrovascular diseases or risk factors:
5. LVEF <50%;
6. NYHA Class III or IV heart failure;
7. History of myocarditis, cardiomyopathy, or myocardial infarction within 6 months prior to enrollment (unless cardiac function has recovered as confirmed by the investigator);
8. Uncontrolled arrhythmias (e.g., atrial fibrillation, ventricular tachycardia) or requiring long-term anti-arrhythmic therapy;
9. QTcF >480 ms on screening ECG;
10. Uncontrolled hypertension (systolic BP >160 mmHg or diastolic BP >100 mmHg);
11. History of ischemic or hemorrhagic stroke (unless stable for >6 months with no sequelae);
12. Uncontrolled intracranial lesions (e.g., brain tumors, aneurysms);
13. History of DVT or PE (unless on stable anticoagulant therapy for ≥6 months);
14. Significantly elevated troponin or BNP/NT-proBNP levels suggestive of potential cardiac injury or dysfunction;
15. • Non-healing wounds or fractures for a prolonged period;
16. • Coagulation disorders or bleeding diathesis;
17. • History of substance abuse (including psychiatric drugs) that cannot be discontinued or history of psychiatric disorders;
18. • Uncontrolled or active fungal, bacterial, viral, or other infections.
19. • Prior anti-tumor treatment-related toxicities not recovered to ≤Grade 1 or to levels specified in the inclusion/exclusion criteria;
20. • Known HIV infection; known active syphilis; or active hepatitis B (HBsAg-positive and HBV-DNA ≥500 IU/mL or above the lower limit of detection, whichever is higher) or hepatitis C (anti-HCV-positive and HCV-RNA above the lower limit of detection);
21. • Uncontrolled pleural effusion, pericardial effusion, or ascites requiring repeated drainage despite appropriate intervention;
22. • Severe allergic reaction history to key study treatments (including fludarabine, cyclophosphamide, mycophenolate sodium, tocilizumab, and anti-infective agents used during preconditioning);
23. • Active autoimmune disease requiring systemic treatment within 2 years (including but not limited to autoimmune hepatitis, uveitis, enteritis, hypophysitis, vasculitis, nephritis, hyperthyroidism); physiologic corticosteroid replacement therapy (e.g., thyroxine, insulin, or corticosteroids for adrenal or pituitary insufficiency) is not considered systemic treatment;
24. • Female participants unwilling to use contraception from informed consent through 6 months after CAR-T cell infusion;
25. • Participants with leptomeningeal metastasis, brainstem metastasis, spinal cord metastasis and/or compression, or active/symptomatic CNS metastases not treated locally;
26. • History of interstitial lung disease (ILD) or non-infectious pneumonitis requiring steroid treatment;
27. • Clinically significant pulmonary impairment due to lung comorbidities, including but not limited to underlying pulmonary disease (e.g., pulmonary embolism, severe asthma, or severe COPD within 3 months prior to enrollment), any autoimmune, connective tissue, or inflammatory disorders involving the lungs (e.g., rheumatoid arthritis, sarcoidosis), or prior pneumonectomy;
28. • Any condition deemed by the investigator to interfere with drug evaluation, participant safety, or study outcomes, or any other condition making the participant unsuitable for the study.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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30 participants in 1 patient group

Single dose injection of REVO-UWD-01

Experimental group

Description:

Dose escalation will be performed for the single dose injection of REVO-UWD-01 for treating mCRC

Treatment:

Biological: Universal CAR-T cells injection for treating mCRC