Skip to content
Bored Studies
RecruitingPhase 3

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

View Study & Apply (opens in a new tab)

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
A Study to Evaluate the Efficacy and Safety of Hetrombopag Olamine… (NCT07286032) | Bored Studies