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A Study to Evaluate the Efficacy and Safety of Hetrombopag Olamine Tablets Vs Placebo in Patients With Chemotherapy-Induced Thrombocytopenia (ExCIT)

RecruitingPhase 3Ages 18 Years - anyAllJiangsu HengRui Medicine Co., Ltd.
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In plain words

What the trial is, and whether it could suit you

The ExCIT study is being conducted to evaluate the efficacy, and safety of of Hetrombopag Olamine Tablets Vs Placebo in Patients with Chemotherapy-Induced Thrombocytopenia.

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
Inclusion Criteria: 1. Male or female, age โ‰ฅ 18 years at screening. 2. Histologically or cytologically confirmed solid tumor (e.g., non-small-cell lung carcinoma \[NSCLC\], breast, ovarian, bladder, pancreatic, gastrointestinal, or colon/colorectal cancer). 3. Receiving platinum- and/or gemcitabine-containing chemotherapy regimens on 14- or 21-day treatment cycles. 4. Platelet count \< 85 x 109/L at enrollment. 5. For Part B, experiencing a chemotherapy delay of โ‰ฅ 7 days due to CIT. 6. At least 2 scheduled chemotherapy cycles of the same treatment regimen as was used prior to enrollment. 7. Eastern Cooperative Oncology Group performance status (ECOG PS) 0-2. 8. Life expectancy โ‰ฅ6 months. 9. Signed ICF for voluntary participation in the study and good compliance. Exclusion Criteria: 1. WHO Grade โ‰ฅ 2 bleeding within 14 days prior to screening. 2. Hematopoietic diseases other than CIT (e.g., primary immune thrombocytopenia). 3. Hematologic malignancies. 4. Thrombocytopenia caused by reasons other than chemotherapy, including but not limited to chronic liver disease, hypersplenism, infection, and hemorrhage, within 6 months prior to Study Day 1. 5. Untreated brain metastases; or with leptomeningeal metastasis. 6. Conditions that require emergent treatment (e.g., superior vena cava syndrome, spinal cord compression). 7. Severe cardiovascular disorders or interventions within 6 months. 8. Have arterial/venous thrombosis with anticoagulation not tolerated for at least 6 weeks. 9. Known bleeding disorders, platelet dysfunction. 10. Severe haemorrhage during screening (e.g., gastrointestinal or intracranial hemorrhage) within 28 days prior to enrolment. 11. Previous treatment with thrombopoietin receptor agonists (TPO-RAs) within 14 days prior to enrolment. 12. Platelet transfusion within 72 hours prior to enrollment. 13. Acute or uncontrolled hepatitis B\&C infection. 14. Human immunodeficiency virus (HIV) infection.
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What it tests

  • Hetrombopag Olamine
  • Hetrombopag Olamine; Hetrombopag Olamine Placebo
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Where

51 sites
Starling Oncology
Long Beach, United States
Cancer and Blood Specialty Clinic
Los Alamitos, United States
UCLA
Los Angeles, United States
Clermont Oncology Center
Clermont, United States
Oncology & Hematology Associates of West Broward
Coral Springs, United States
Starling Oncology / Oncology Institute of Hope & Innovation
Miami, United States
Mid-Florida Hematology & Oncology Centers, P.A.
Orange City, United States
Springfield Clinic
Springfield, United States

โ€ฆand 43 more on ClinicalTrials.gov.

๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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