Herombopag for the Prevention of Radio-chemotherapy Induced Thrombocytopenia in Cervical Cancer

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexFemale
Age18+
SponsorPeking University Cancer Hospital & Institute

About this trial

Exploring and evaluating the efficacy of herombopag in preventing thrombocytopenia due to radiotherapy for cervical cancer

Eligibility criteria

Qualifiers

Volunteer to participate in the trial and sign the informed consent

Pathologically or cytologically confirmed cervical cancer

aged 18 years or older

ECOG performance score 0-1

Disqualifiers

Participants with other diseases of hematopoietic system, including but not limited to leukemia, primary immune thrombocytopenia, myeloproliferative diseases, multiple myeloma, and myelodysplastic syndrome

Participants with thrombocytopenia occurred within the last 6 months due to causes other than CTIT, including but not limited to chronic liver disease, hypersplenism, infection

Bone marrow invasion or metastasis

History of severe cardiovascular disease within the last 6 months, such as congestive heart failure (NYHA heart function score III-IV), arrhythmias known to increase the risk of thromboembolism such as atrial fibrillation, after coronary stenting, angioplasty, and para-coronary transplantation, etc

Trial design

Treatments tested in this trial

  • herombopag

Treatment groups

30 Participants
are divided into 1 treatment group