OncoMatch

OncoMatch/Clinical Trials/NCT07718490

Immunotheray Combined With Simvastatin and Target Therapy and Chemotharepy for Advanced Colorectal Cancer

Is NCT07718490 recruiting? Yes, currently enrolling (Sep 2026). This Phase 2 trial studies Adebrelimab for metastatic colorectal cancer.

Phase 2RecruitingThe First Affiliated Hospital with Nanjing Medical UniversityNCT07718490Data as of Sep 2026Location: China

Treatment: AdebrelimabMetastatic colorectal cancer with microsatellite instability-high (MSI-H) or mismatch repair-deficient (dMMR) molecular phenotypes could significantly benefit from immune checkpoint inhibitor therapy, ushering in the MSI era of immunotherapy for colorectal cancer. However, MSI-H/dMMR is present in only 15%-20% of stage II/III and 5% of stage IV colorectal cancer patients, while the vast majority of patients exhibit microsatellite stability (MSS) or proficient mismatch repair (pMMR) types, which are insensitive to immunotherapy. Therefore, how to enhance the efficacy of immunotherapy in the pMMR/MSS population through combination therapy has become a hotspot and challenge in colorectal cancer research.

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Extracted eligibility criteria

Treatments studied

Immunotherapy

Adebrelimab

Cancer type

Colorectal Cancer

Biomarker criteria

Required: Mismatch-repair proficient (pMMR / MSS)

MSS/ PMMR-type advanced colorectal cancer

Disease stage

Metastatic disease required

Performance status

ECOG 0–1(Restricted strenuous activity)

Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1

Demographics

Ages ≤ 75

Prior therapy

Max 0 prior lines

Cannot have received: systemic anti-tumor therapy

Exception: neoadjuvant/adjuvant therapy allowed if time from last chemotherapy to recurrence or progression is more than 6 months

No prior systemic anti-tumor therapy; patients who have received neoadjuvant/adjuvant therapy are eligible if the time from the last chemotherapy to recurrence or progression is more than 6 months

Lab requirements

Blood counts

absolute neutrophil count (anc) ≥1.5×10^9/l; platelet count ≥100×10^9/l; hemoglobin ≥9 g/dl; serum albumin ≥2.5 g/dl

Kidney function

serum creatinine ≤1.5 × uln, or creatinine clearance >60 ml/min (calculated by cockcroft-gault formula)

Liver function

total bilirubin ≤1.5 × uln; alt and ast ≤2.5 × uln, or ≤5 × uln in the presence of liver metastases

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT07718490 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior systemic anti-tumor therapy disqualifies patients from enrollment.

Does this trial require MSH6?

Yes, MSH6 wild-type is a required biomarker for enrollment.

Does this trial require MLH1?

Yes, MLH1 wild-type is a required biomarker for enrollment.

Does this trial require MSH2?

Yes, MSH2 wild-type is a required biomarker for enrollment.

Is there an age limit?

Yes. Patients must be 75 years or younger.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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