Sequential Hetrombopag and Recombinant Human Thrombopoietin for Cancer Therapy-Induced Thrombocytopenia
A Multicenter, Exploratory Clinical Study of Sequential Hetrombopag and Recombinant Human Thrombopoietin for Cancer Therapy-Induced Thrombocytopenia
This is a multicenter, randomized, exploratory clinical study. The study plans to enroll 96 participants with cancer therapy-induced thrombocytopenia. participants will be stratified by baseline platelet countand randomized 1:1 to the hetrombopag sequential group (Experimental Group A) or the recombinant human thrombopoietin (rhTPO) group (Experimental Group B).
연구 개요
상태
상태
정황
정황
개입 / 치료
개입 / 치료
연구 유형
연구 유형
등록 (추정된)
등록
단계
단계
- 2 단계
연락처 및 위치
연구 연락처
연구 연락처
- 이름: Zhengzheng Shan
- 전화번호: +86-15639934037
- 이메일: sally900603@126.com
참여기준
자격 기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- Age 18-75 years (inclusive), male or female;
- Patients with histologically or cytologically confirmed malignant tumors, including but not limited to lung cancer, breast cancer, colorectal cancer, gastric cancer, etc.;
- Currently receiving anticancer therapy in 21-day cycles, with grade 3 or higher thrombocytopenia during treatment, and expected to be able to receive the current anticancer regimen for ≥ 1 more cycle;
- ECOG PS score 0-2;
- With permitted use of red blood cells, erythropoietin, and recombinant human granulocyte colony-stimulating factor consistent with routine clinical practice: absolute neutrophil count (ANC) ≥ 1.0×10^9/L and hemoglobin (Hb) ≥ 80 g/L;
- No significant hepatic impairment;
- No significant renal impairment;
- Expected survival ≥ 12 weeks;
- Female participants of childbearing potential must have a negative serum pregnancy test within 7 days before the first dose, must not be lactating, and must agree to use effective contraception during the study and for 7 days after the last dose of study drug; male participants whose partners are women of childbearing potential must be surgically sterilized or must agree to use reliable contraception from the signing of the informed consent form until 7 days after the last dose of study drug;
- Voluntary participation in this study with signed informed consent and good compliance.
Exclusion Criteria:
- Concomitant hematopoietic system diseases, including but not limited to leukemia, primary immune thrombocytopenia, myeloproliferative neoplasms, multiple myeloma, and myelodysplastic syndromes;
- Other diseases causing thrombocytopenia other than cancer therapy-induced thrombocytopenia (CTIT) within 6 months before randomization, including but not limited to chronic liver disease and hypersplenism;
- Uncontrolled active infection;
- Tumor bone marrow invasion or bone marrow metastasis;
- Severe cardiac clinical symptoms or diseases within 6 months before randomization;
- Arterial or venous thrombotic events (stroke, transient ischemic attack, myocardial infarction, deep vein thrombosis, or pulmonary embolism) within 3 months before randomization, or clinical symptoms and history suggestive of thrombophilia;
- Concomitant severe bleeding symptoms or clear clinical manifestations of bleeding tendency, such as gastrointestinal or cerebral hemorrhage;
- Conditions affecting drug absorption (e.g., dysphagia, history of total gastrectomy);
- Receipt of whole-pelvis, whole-spine, or extensive sternal radiotherapy in the previous cycle or expected during the current cycle;
- Treatment with rhIL-11, rhTPO and/or TPO-RA drugs within 7 days before randomization;
- Treatment with romiplostim or romiplostim N01 within 1 month before randomization;
- Platelet transfusion within 3 days before randomization;
- Known or expected allergy or intolerance to the active ingredients or excipients of the study drug;
- Known history of positive human immunodeficiency virus (HIV) test or acquired immunodeficiency syndrome (AIDS);
- Known active viral hepatitis;
- Any other condition that, in the investigator's opinion, poses a significant risk to the subject's health or safety or may affect the efficacy evaluation.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 없음(오픈 라벨)
팔의 수
무기와 개입
참가자 그룹 / 팔참가자 그룹 / 팔 |
개입 / 치료개입 / 치료 |
|---|---|
|
실험적: Hetrombopag sequential group
|
hetrombopag (orally) + rhTPO (subcutaneous injection) |
|
실험적: Recombinant human thrombopoietin group
|
rhTPO (subcutaneous injection) |
연구는 무엇을 측정합니까?
주요 결과 측정
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Response rate
기간: Up to 6 weeks
|
Proportion of participants achieving treatment response |
Up to 6 weeks
|
2차 결과 측정
2차 결과 측정
결과 측정 |
기간 |
|---|---|
|
부작용
기간: 최대 8주
|
최대 8주
|
|
the proportion of participants whose platelet count recovers to ≥ 80×10^9/L
기간: Up to 14 days
|
Up to 14 days
|
|
the proportion of participants whose platelet count recovers to ≥ 100×10^9/L
기간: Up to 14 days
|
Up to 14 days
|
|
Time to first platelet count ≥ 80×10^9/L
기간: Up to 3 weeks
|
Up to 3 weeks
|
|
Platelet counts at each visit
기간: From randomization up to the end of Cycle 1 of on-study anti-tumor therapy (each cycle is 21 days)
|
From randomization up to the end of Cycle 1 of on-study anti-tumor therapy (each cycle is 21 days)
|
|
Proportion of participants receiving at least one platelet-raising rescue therapy
기간: From randomization up to the end of Cycle 1 of on-study anti-tumor therapy (each cycle is 21 days)
|
From randomization up to the end of Cycle 1 of on-study anti-tumor therapy (each cycle is 21 days)
|
|
Bleeding events
기간: From randomization up to the end of Cycle 1 of on-study anti-tumor therapy (each cycle is 21 days)
|
From randomization up to the end of Cycle 1 of on-study anti-tumor therapy (each cycle is 21 days)
|
공동 작업자 및 조사자
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
연구 시작
기본 완료 (추정된)
기본 완료
연구 완료 (추정된)
연구 완료
연구 등록 날짜
최초 제출
최초 제출
QC 기준을 충족하는 최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
처음 게시됨
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
마지막 업데이트 게시됨
QC 기준을 충족하는 마지막 업데이트 제출
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
기타 연구 ID 번호
- 2026-KY-1560
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
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