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OncoMatch/Clinical Trials/NCT07389629

Iparomlimab and Tuvonralimab (QL1706) Combination With Lenvatinib as Neoadjuvant Therapy for ccRCC

Is NCT07389629 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies QL1706 Combined With Lenvatinib for iparomlimab and tuvonralimab.

Phase 2RecruitingSun Yat-sen UniversityNCT07389629Data as of Jun 2026Location: China

Treatment: QL1706 Combined With LenvatinibThrough the combination of aparolitovorelli monoclonal antibody and lenvatinib neoadjuvant therapy, partial nephrectomy can be successfully and safely performed in patients with localized renal cell carcinoma (T1N0M0 or T2N0M0) who have indications for kidney preservation surgery but have difficulty in preserving the kidney (R.E.N.A.L. score \>= 10).

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Extracted eligibility criteria

Treatments studied

Targeted therapy

QL1706 Combined With Lenvatinib

Cancer type

Renal Cell Carcinoma

Disease stage

Required: Stage T1N0M0, T2N0M0

Performance status

ECOG 0–1(Restricted strenuous activity)

Demographics

Ages ≤ 80

Prior therapy

Cannot have received: Chinese herbal medicine or immunomodulatory drugs with anti-tumor indications

Received Chinese herbal medicine or immunomodulatory drugs with anti-tumor indications within 14 days prior to the first use of the investigational drug

Cannot have received: systematic treatment (including thymosin, interferon, interleukin, except for local use to control pleural effusion)

Exception: local use to control pleural effusion

Perform systematic treatment (including thymosin, interferon, interleukin, except for local use to control pleural effusion)

Lab requirements

Blood counts

ANC >= 1.5 × 10^9/L (1500/mm^3); Platelet count >= 100 × 10^9/L (100000/mm^3); Hemoglobin >= 90 g/L

Liver function

Serum total bilirubin (TBIL) <= 1.5 × ULN; ALT and AST <= 2.5 × ULN; for subjects with liver metastases, AST and ALT <= 5 × ULN, serum albumin (ALB) >= 28g/L

Good organ function, screening laboratory test results meet the following criteria: (1) Hematology... (2) Liver... Coagulation function: INR and APTT <= 1.5 × ULN

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

Frequently asked questions

Is NCT07389629 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior Chinese herbal medicine or immunomodulatory drugs with anti-tumor indications, systematic treatment (including thymosin, interferon, interleukin, except for local use to control pleural effusion) disqualifies patients from enrollment.

What disease stage is eligible?

Stage T1N0M0 or T2N0M0 is required.

Is there an age limit?

Yes. Patients must be 80 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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