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A randomized, open, parallel controlled, single-center clinical trial for recombinant human erythropoietin injection (CHO cells) in the treatment of anemia caused by chemotherapy in non-bone marrow malignant tumors at different times

A randomized, open, parallel controlled, single-center clinical trial for recombinant human erythropoietin injection (CHO cells) in the treatment of anemia caused by chemotherapy in non-bone marrow malignant tumors at different times

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900024947
Enrollment
Unknown
Registered
2019-08-04
Start date
2019-08-01
Completion date
Unknown
Last updated
2019-08-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tumor anemia

Interventions

control group:Recombinant human erythropoietin injection (Jimaixin) 12000 IU/branch, one subcutaneous injection, three times a week (at least one day interval each time) for 8 weeks
experimental group:Recombinant human erythropoietin injection (Jimaixin) 12000 IU/branch, 3 branches per time, subcutaneous injection, once a week (3 branches per injection at different parts), for 8

Sponsors

Anyang Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1) Patients with non-bone marrow malignant tumors (excluding leukemia and multiple myeloma) diagnosed by cytology/histology; 2) Chemotherapy-related anemia (Hb =60) and expected survival of more than 3 months; 4) patients weighing more than 45 kg; 5) Aged 18-70 years, gender-free, hospitalized or outpatient patients; 6) Voluntary subjects, patients who have signed the informed consent.

Exclusion criteria

Exclusion criteria: 1) Patients with breast cancer and head and neck cancer. 2) Anemia caused by iron, folic acid or B12 deficiency and metabolic disorders, hemolysis, acute or chronic blood loss or other non-chemotherapy causes (iron deficiency criteria: ferritin 160mmHg, DP > 110 mmHg) or severe infection. 9) Patients with severe primary diseases of heart, liver, kidney and hematopoietic system (ALT, AST > 2.5 times of the upper limit of normal value, Cr > the upper limit of normal value; ALT, AST > 3 times of the upper limit of normal value in patients with liver metastasis). 10) Those with neurological or mental disorders who are unable to cooperate or unwilling to cooperate. 11) Patients with previous history of thrombosis, abnormal coagulation function, hematological history or ineffective EPO treatment. 12) Patients with allergies and allergic constitutions to known ingredients of test or control drugs. 13) Pregnant, lactating women or recent patients with fertility plans. 14) Patients who have participated in other clinical trials in the past three months.

Design outcomes

Primary

MeasureTime frame
hemoglobin;

Countries

China

Contacts

Public ContactWang Huixiao

Anyang Cancer Hospital

13503723589@163.com+86 13503723589

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026