Hetrombopag or Placebo in Treatment-Naive Severe Aplastic Anemia
Study Details
Study Description
Brief Summary
This is a multicenter, randomized, placebo-control, phase III study to investigate hetrombopag in subjects with severe AA who are treated naive.
180 treated naive patients with SAA will be enrolled in the study. The primary objective of the study will be the rate of complete hematologic response at six months.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 3 |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Hetrombopag Olamine+Standard Therapy
|
Drug: Hetrombopag Olamine+Standard Therapy
once daily
|
| Placebo Comparator: Placebo+Standard Therapy
|
Drug: Placebo+Standard Therapy
once daily
|
Outcome Measures
Primary Outcome Measures
- Rate of complete hematologic response at six months. [6 months]
Eligibility Criteria
Criteria
Inclusion Criteria:
1.15 Years to 75 Years (weight greater than 50 kg if Age < 18 years old). 2.Severe aplastic anemia characterized by Bone marrow cell proliferation less than 25 percent (If ≥25% but <50%, the remaining hematopoietic cells should be <30%) AND At least two of the following: Absolute neutrophil count <0.5×109/L; Platelet count <20×109/L; Absolute reticulocyte count <20×109/L.
3.Unsuitable or unwilling to perform hematopoietic stem cell transplantation (HSCT).
4.Signed informed consent.
Exclusion Criteria:
-
Diagnosis of whole blood cell reduction due to other causes or bone marrow hypoproliferative diseases.
-
Subjects who have previously received immunosuppressive therapy with mycophenolate mofetil, sirolimus, high dose cyclophosphamide (≥45mg/kg/d), alemtuzumab, etc；or have treated with thrombopoietin receptor agonist (eg, eltrombopag, romiplostim, rhTPO, etc.) prior to randomization.
-
Previous history of hematopoietic stem cell transplantation.
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Subjects who is known or suspected of contraindications or hypersensitivity to Hetrombopag's API (Active Pharmaceutical Ingredient).
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Evidence of clonal cytogenetic abnormalities at the time of screening.
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Bleeding and/or Infection not adequately responding to appropriate therapy.
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Any laboratory or clinical evidence for HIV infection. Any clinical history for hepatitis C infection; chronic hepatitis B infection; or any evidence for active hepatitis at the time of subjects screening.
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ALT> 2.5 x upper limit of normal (ULN), AST> 2.5 x upper limit of normal (ULN) DBLI> 1.5 x upper limit of normal (ULN), Scr> upper limit of normal (ULN).
-
Subjects with uncontrolled hypertension (>180/100mmHg), severe arrhythmia (such as complete left bundle branch block, QT interval prolongation (Bazetts formula), torsade ventricular tachycardia, etc.), unstable angina, pulmonary hypertension at the time of screening.
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Subjects diagnosed with cirrhosis or portal hypertension.
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Subjects with malignant solid tumors of any organ system within 5 years prior to screening, with or without treatment, metastasis or recurrence, except for local cutaneous basal cell carcinoma; subjects with hematological tumors found previously or during screening.
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Subjects with deep vein thrombosis, myocardial infarction, stroke or peripheral arterial embolization within 12 months prior to randomization.
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Female subjects who are nursing or pregnant.
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Subjects cannot comply with effective contraception.
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Subjects have participated in other clinical trial within the 3 months prior to study entry.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Blood Diseases Hospital, Chinese Academy of Medical Sciences | Tianjin | Tianjin | China | 300041 |
Sponsors and Collaborators
- Jiangsu HengRui Medicine Co., Ltd.
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- HR-TPO-SAA-III