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OncoMatch/Clinical Trials/NCT04501718

Apatinib Combined with Temozolomide and Etoposide Capsules in the Treatment of Recurrent Medulloblastoma in Children

Is NCT04501718 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies Apatinib Combined With Temozolomide and Etoposide Capsules for recurrent medulloblastoma.

Phase 2RecruitingBeijing Sanbo Brain HospitalNCT04501718Data as of Jun 2026Location: China

Treatment: Apatinib Combined With Temozolomide and Etoposide CapsulesThis study is a prospective single-center clinical study, which aims to observe and evaluate the efficacy and safety of apatinib combined with temozolomide and oral etoposide in the treatment of recurrent medulloblastoma in children.

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Extracted eligibility criteria

Treatments studied

Other

Apatinib Combined With Temozolomide and Etoposide Capsules

Cancer type

Glioblastoma

Demographics

Ages 2–21

Prior therapy

Must have received: radiation therapy

The time interval from the last radiotherapy is ≥4 weeks.

Must have received: chemotherapy

The time interval from the last chemotherapy is ≥4 weeks, and the patients have fully recovered from the acute toxicity of the last treatment. If you receive nitrosourea chemotherapeutics before enrollment, the interval between enrollment and the last chemotherapy is ≥6 weeks.

Must have received: surgery

After biopsy or surgery, the first postoperative pathological diagnosis is medulloblastoma.

Cannot have received: anti-tumor angiogenesis drugs

Past application of anti-tumor angiogenesis drugs

Lab requirements

Blood counts

HGB≥100g/L; WBC≥3.0×10^9/L; NEUT≥1.5×10^9/L; PLT ≥100×10^9/L; no blood transfusion within 14 days

Kidney function

Serum Cr≤1.5x ULN or endogenous creatinine clearance ≥50ml/min (Cockcroft-Gault formula)

Liver function

BIL≤1.5x ULN; ALT and AST≤2.0x ULN

Cardiac function

ECG: heart rate 55-100 bpm, QTc<480ms, T wave normal or low, ST segment normal or non-specific changes

The main organ functions are normal, and there is no serious blood, heart, lung, liver, kidney dysfunction and immune deficiency diseases. The laboratory inspection meets the following requirements: ... (see above for details)

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

Frequently asked questions

Is NCT04501718 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior anti-tumor angiogenesis drugs disqualifies patients from enrollment.

Is there an age limit?

Yes. Patients must be 21 years or younger and at least 2 years old.

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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Related pages

Glioblastoma trials