A Study to Evaluate the Efficacy and Safety of Hetrombopag Olamine Tablets Vs Placebo in Patients With Chemotherapy-Induced Thrombocytopenia (ExCIT)
Jiangsu HengRui Medicine Co., Ltd. · NCT07286032
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Phase 3
- Target enrollment
- 150
- US sites recruiting
- 8
- Study start
- April 16, 2026
- Record last updated
- October 1, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
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.
Being studied: Hetrombopag Olamine; Hetrombopag Olamine; Hetrombopag Olamine Placebo
Conditions: Patients With Chemotherapy-Induced Thrombocytopenia
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Male or female, age ≥ 18 years at screening.
- Histologically or cytologically confirmed solid tumor (e.g., non-small-cell lung carcinoma [NSCLC], breast, ovarian, bladder, pancreatic, gastrointestinal, or colon/colorectal cancer).
- Receiving platinum- and/or gemcitabine-containing chemotherapy regimens on 14- or 21-day treatment cycles.
- Platelet count \< 85 x 109/L at enrollment.
- For Part B, experiencing a chemotherapy delay of ≥ 7 days due to CIT.
- At least 2 scheduled chemotherapy cycles of the same treatment regimen as was used prior to enrollment.
- Eastern Cooperative Oncology Group performance status (ECOG PS) 0-2.
- Life expectancy ≥6 months.
- Signed ICF for voluntary participation in the study and good compliance.
Exclusion Criteria
- WHO Grade ≥ 2 bleeding within 14 days prior to screening.
- Hematopoietic diseases other than CIT (e.g., primary immune thrombocytopenia).
- Hematologic malignancies.
- 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.
- Untreated brain metastases; or with leptomeningeal metastasis.
- Conditions that require emergent treatment (e.g., superior vena cava syndrome, spinal cord compression).
- Severe cardiovascular disorders or interventions within 6 months.
- Have arterial/venous thrombosis with anticoagulation not tolerated for at least 6 weeks.
- Known bleeding disorders, platelet dysfunction.
- Severe haemorrhage during screening (e.g., gastrointestinal or intracranial hemorrhage) within 28 days prior to enrolment.
- Previous treatment with thrombopoietin receptor agonists (TPO-RAs) within 14 days prior to enrolment.
- Platelet transfusion within 72 hours prior to enrollment.
- Acute or uncontrolled hepatitis B\&C infection.
- Human immunodeficiency virus (HIV) infection.
Recruiting US locations
Cancer and Blood Specialty Clinic
Los Alamitos, CA 90254
Site contact: Arati Chand
UCLA
Los Angeles, CA 90095
Site contact: Wanxing Chai-Ho
Clermont Oncology Center
Clermont, FL 34711
Site contact: Gopal Kunta
Oncology & Hematology Associates of West Broward
Coral Springs, FL 33065
Site contact: Sumit Sawhney
Mid-Florida Hematology & Oncology Centers, P.A.
Orange City, FL 32763
Site contact: Santosh Nair
Springfield Clinic
Springfield, IL 62702
Site contact: Preet Singh
University of Iowa
Iowa City, IA 52242
Site contact: Naomi Fei
Cancer Partners of Nebraska
Lincoln, NE 68516
Site contact: Irfan Vaziri
Study contacts (from the official record)
- Brian Yu, MD · +86 400 828 3900 · brian.yu@hengrui.com
- Junye Xiong, MD · +86-0518-82342973 · junye.xiong.jx9@hengrui.com