A Multicenter Randomized Controlled Study on the Treatment of Refractory CTIT With Romiplostim N01 Compared to Recombinant Human Thrombopoietin

Inclusion Criteria:

1. Sign a written informed consent form before enrollment;

2. Age range from 18 to 75 years old;

3. Solid tumors or hematological tumors confirmed by tissue or pathology;

4. CTIT patients caused by anti-tumor therapy;

5. At least 2 weeks of treatment with two types of platelet growth factors and noresponse (including rhTPO or TPO-RA)

6. Have not received treatment with Roptistine/Roptistine N01;

7. ECOG PS score: 0-2;

8. Platelet value<30 × 109/L;

9. Estimated survival time during screening is ≥ 12 weeks;

10. Subjects of childbearing age agree to take reliable contraceptive measures (including male or female condoms, contraceptive foam, contraceptive gel,contraceptive film, contraceptive cream, contraceptive suppository, abstinence andthe placement of intrauterine devices, etc.) throughout the study period; Excludingfemale participants who have undergone hysterectomy, bilateral salpingectomy,bilateral tubal ligation, or more than 1 year after menopause, as well as maleparticipants who have undergone bilateral salpingectomy or ligation;

11. Voluntarily participate in this study, sign an informed consent form, and have goodcompliance.

Exclusion Criteria:

• Patients with any of the following conditions are not eligible for inclusion in this study:

1. Suffering from hematopoietic system diseases other than thrombocytopenia (CIT)caused by tumor chemotherapy drugs, including but not limited to leukemia, primaryimmune thrombocytopenia, myeloproliferative diseases, multiple myeloma, andmyelodysplastic syndrome;

2. Screening for thrombocytopenia caused by causes other than CIT within the first 6months, including but not limited to chronic liver disease, splenic hyperfunction,infection, and bleeding;

3. Bone marrow invasion or metastasis;

4. Have received pelvic and spinal radiation therapy, as well as bone field radiationtherapy, or are currently/expected to receive radiation therapy within the threemonths prior to screening;

5. Screening for a history of severe cardiovascular disease within the first 6 months,such as congestive heart failure (NYHA heart function score III-IV), knownarrhythmias that increase the risk of thromboembolism, such as atrial fibrillation,after coronary stent implantation, angioplasty, and coronary artery bypass grafting;

6. Any history of arterial or venous thrombosis occurring within the first 6 months ofscreening;

7. Screening for clinical manifestations of severe bleeding within the first two weeks,such as gastrointestinal or central nervous system bleeding;

8. Brain tumors or brain metastases;

9. Urgent treatment is required, such as vena cava syndrome and spinal cord compressionsyndrome;

10. Neutrophil absolute value < 1.0 × 109/L, hemoglobin < 80g/L, allowing the use ofgranulocyte colony-stimulating factors and red blood cells that comply with clinicalnorms EPO infusion therapy;

11. Significant abnormalities in liver function: patients without liver metastasis,ALT/AST>3ULN (upper limit of normal value), TBIL>3ULN； Patients with livermetastasis are present, ALT/AST≥5ULN，TBIL≥5ULN；

12. Renal dysfunction: blood creatinine ≥ 1.5ULN or eGFR ≤ 60 ml/min (Cockcroft Gaultformula);

13. Within the first month prior to screening, patients who have received treatment withloperstine/loperstine N01 or recombinant human thrombopoietin (rhTPO);

14. Received platelet transfusion within the first 3 days of randomization;

15. Patients who are known or expected to be allergic or intolerant to Roxetine N01 orrhTPO excipients

16. HIV infected individuals;

17. Pregnant or lactating women;

18. Participated in any clinical study of any other investigational drug or device threemonths prior to screening;

19. The researchers believe that participating in the trial poses a significant risk tothe health or safety of the subjects, or other circumstances that may affect theefficacy evaluation.