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OncoMatch/Clinical Trials/NCT05069857

Neoadjuvant Personalized Anti-PD-1 and Anti-VEGFR Therapy in OSCC Patients

Is NCT05069857 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies multiple treatments including Camrelizumab (anti-PD-1 inhibitor) and Apatinib (anti-VEGFR inhibitor) for oral squamous cell carcinoma.

Phase 2RecruitingShanghai Jiao Tong University School of MedicineNCT05069857Data as of Jun 2026Location: China

Treatment: Camrelizumab (anti-PD-1 inhibitor) · Apatinib (anti-VEGFR inhibitor)To evaluate the efficacy of neoadjuvant anti-PD-1 plus anti-VEGFR therapy for patients with locally advanced and resectable oral squamous cell carcinoma, and the CPS\>10 in the biopsy samples.

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Extracted eligibility criteria

Treatments studied

Other

Camrelizumab (anti-PD-1 inhibitor)Apatinib (anti-VEGFR inhibitor)

Cancer type

Head and Neck Squamous Cell Carcinoma

Biomarker criteria

Required: PD-L1 (CD274) expression > 10 CPS (CPS score > 10)

The combined positive score (CPS score) of PD-L1 expression > 10

Disease stage

Required: Stage III, IVA

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Demographics

Ages ≤ 75

Prior therapy

Cannot have received: radiation therapy

Lab requirements

Blood counts

WBC ≥ 3,000/mm3, hemoglobin ≥ 8g/L, platelet ≥ 80,000/mm3

Kidney function

serum creatinine ≤ 1.5 times the normal upper limit

Liver function

ALAT/ASAT ≤ 2.5 times the normal upper limit, bilirubin ≤ 1.5 times the normal upper limit

Cardiac function

No obvious cardiovascular abnormalities (such as myocardial infarction, superior vena cava syndrome, ≥ grade 2 heart disease diagnosed according to the NYHA classification criteria within 3 months prior to enrollment)

Blood routine examination: WBC < 3,000/mm3, hemoglobin < 8g/L, platelet < 80,000/mm3; Liver function: ALAT/ASAT > 2.5 times the normal upper limit, bilirubin > 1.5 times the normal upper limit; Renal function: serum creatinine > 1.5 times the normal upper limit; Obvious cardiovascular abnormalities (such as myocardial infarction, superior vena cava syndrome, ≥ grade 2 heart disease diagnosed according to the NYHA classification criteria within 3 months prior to enrollment)

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

Frequently asked questions

Is NCT05069857 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior radiation therapy disqualifies patients from enrollment.

Does this trial require CD274?

Yes, CD274 expression > 10 CPS is a required biomarker for enrollment.

What disease stage is eligible?

Stage III or IVA is required.

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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