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An observational study for Herombopag Olamine Tablets in the treatment of thrombocytopenia resulted from the antitumor therapy of breast cancer

An observational study for Herombopag Olamine Tablets in the treatment of thrombocytopenia resulted from the antitumor therapy of breast cancer

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100053670
Enrollment
Unknown
Registered
2021-11-27
Start date
2021-12-27
Completion date
Unknown
Last updated
2023-01-23

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

Conditions

Thrombocytopenia resulted from the antitumor therapy of breast cancer

Interventions

Herombopag Olamine group:Nil

Sponsors

The First Affiliated Hospital of Soochow University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Men and women greater than or equal to 18 years of age; 2. Participants must have histologically or cytologically confirmed breast cancer; 3. Platelet count<50x10^9/L during the current anti-tumor treatment cycle, and could accept the current anti-tumor treatment plan for at least 1 cycle; 4. ECOG performance status 0-2; 5. Volunteer to join this study and sign an informed consent form; have good treatment compliance; 6. Sign an informed consent form to participate in the experimental treatment.

Exclusion criteria

Exclusion criteria: 1. Suffer from the following hematopoietic system diseases caused by tumor anti-tumor drugs other than thrombocytopenia , including but not limited to leukemia, primary immune thrombocytopenia, bone marrow proliferative diseases, multiple myeloma, and myelodysplastic syndromes, etc. 2. Thrombocytopenia caused by non-antitumor therapy in the 6 months before screening, including but not limited to chronic liver disease, hypersplenism, infection, and bleeding; 3. Bone marrow invasion or bone marrow metastasis; 4. Have received pelvic, spinal radiotherapy and osseous field irradiation within 3 months before screening, or are currently/expected to receive radiotherapy; 5. Have received thrombopoietin receptor agonists (such as eltrombopag, romiplostim), or recombinant human thrombopoietin(rhTPO), recombinant human interleukin-11 (rhIL-11) during the current anti-tumor treatment cycle )treatment; 6. Have received platelet transfusion within 3 days before screening 7. Those who have been confirmed to be allergic to Herombopag and/or its excipients; 8. Pregnant or breastfeeding women; 9. Patients who are participating in other clinical trials; 10. Doctors evaluate patients who are not suitable for inclusion.

Design outcomes

Primary

MeasureTime frame
platelet count;

Countries

China

Contacts

Public ContactGuo Zhaoji

the First Affiliated Hospital of Soochow University

2468412472@qq.com+86 13375183850

Outcome results

None listed

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