A Multicenter, Open-label, Randomized Controlled Trial Evaluating the Efficacy and Safety of Romiplostim N01 in the Treatment of Thrombocytopenia Associated With Concurrent/Sequential Chemoradiotherapy and Chemotherapy Combined With/Without Immunotherapy in Solid Tumors

Jun wang

Status: Not yet enrolling

Conditions: Thrombocytopenia; CTIT-Chemotherapy Induced Thrombocytopenia; Solid Tumor Malignancies, Cancer

Treatments: Drug: Human Interleukin-11; Drug: Romiplostim N01

Study type: Interventional

Funder types: Other

Identifiers

NCT07185893

2025KY020

Details and patient eligibility

About

The purpose of this clinical trial is to evaluate the safety and efficacy of Romiplostim N01 in patients with solid tumors who are undergoing concurrent/sequential radiotherapy and chemotherapy（combined with/without immunotherapy）-related thrombocytopenia.

All eligible patients will be stratified and randomly assigned based on baseline platelet count（Stratification factors: whether the baseline platelet count of the patients is greater than 50×10^9/L. ） . All patients will be randomly assigned in a 1:1 ratio to experimental group or control group:

Experimental group: Romiplostim N01 (N=53) Control group：Human Interleukin-11(rhlL-11) (N=53) The main questions this trial aims to answer are: 1. The proportion of patients who received platelet transfusion due to thrombocytopenia during the treatment process, as well as the adjustment, delay and discontinuation of radiotherapy and chemotherapy doses； 2. Can patients treated with Romiplostim N01 restore their platelet count to ≥ 100×10^9/L and what is the response rate of patients during the treatment (response criteria: no need for platelet transfusion and PLT increase ≥ 50×10^9/L or at least twice the baseline or PLT increase to ≥ 100×10^9/L)；3. The safety and tolerance of Romiplostim N01 in treating CTIT.

Enrollment: 106 estimated patients

Sex: All

Ages: 18 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Age:18 to 80 years old (man or female);
2. Confirmed with solid tumor by pathological histology or cytology examination;
3. The patient is undergoing concurrent/sequential radiotherapy ± immunotherapy;
4. During the treatment period, the patient experienced a decrease in platelets, and the platelet count within the last 3 days before enrollment was 25×10^9/L < platelet count ≤ 75×10^9/L;
5. The estimated survival period at screening is ≥ 3 months, and it is expected that the current chemotherapy cycle can be used for ≥ 2 cycles;
6. ECOG 0 - 2;
7. Fully understand and comply with the requirements of this study, and voluntarily sign the informed consent form.

Exclusion criteria

1. Platelet count ≤ 25×10^9/L at baseline;
2. The patient has previously received treatments for thrombocytopenia, such as thrombopoietin receptor agonists (TOP-RA), recombinant human thrombopoietin (rhTPO), or rhIL-11, etc.;
3. Patients with hematological disorders, including lymphoma, leukemia, aplastic anemia, primary immune thrombocytopenia, myelodysplastic syndromes, multiple myeloma, and myelodysplastic syndrome, etc.;
4. Have experienced thrombocytopenia due to non-tumor treatment within the past 6 months, including but not limited to EDTA-dependent pseudo-thrombocytopenia, splenomegaly, infection, bleeding, etc.;
5. After red blood cell or erythropoietin (EPO) infusion, hemoglobin is still < 50g/L, or after granulocyte colony-stimulating factor (G-CSF) treatment, absolute neutrophil count is still < 1.0×10^9/L;
6. Have experienced any arterial or venous thrombosis within the past 6 months;
7. Have suffered from severe cardiovascular diseases (such as NYHA cardiac function class III-IV), increased risk of thrombosis-related arrhythmias (such as atrial fibrillation), coronary artery stent implantation, angioplasty, and coronary artery bypass grafting within the past 6 months;
8. Have received platelet transfusion within 5 days before randomization or enrollment;
9. Patients with positive hepatitis C antibody and excessive HCV-RNA detection, positive hepatitis B surface antigen and excessive HBV-DNA detection, patients with severe cirrhosis, positive HIV antibody, or positive syphilis antibody;
10. During screening, for subjects without liver metastasis, alanine aminotransferase (ALT) and aspartate aminotransferase (AST) are ≥ 3 times ULN; for subjects with liver metastasis, ≥ 5 times ULN;
11. Serum creatinine concentration ≥ 1.5 times ULN or eGFR ≤ 60ml/min;
12. Patients who are allergic or intolerant to the active ingredient or excipients of Romiplostim N01 for injection;
13. Planning to get pregnant or in the lactation period;
14. The investigator determines that the patient is not suitable to participate in this trial.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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106 participants in 2 patient groups

Romiplostim N01

Experimental group

Description:

Administer Romiplostim N01 subcutaneously in the abdominal area. The initial dose is 3 μg/kg, once a week. The subsequent dose will be adjusted according to the patient's platelet count

Treatment:

Drug: Romiplostim N01

Human Interleukin-11

Active Comparator group

Description:

Human Interleukin-11 for Injection (rhlL-11) 25 - 50 μg/kg, subcutaneous injection, once a day, for at least 7 - 10 days.

Treatment:

Drug: Human Interleukin-11