Summary

Eligibility
for people ages 18 years and up (full criteria)
Location
at UCLA
Dates
study started
study ends around
Principal Investigator
by Wanxing Chai-Ho (ucla)

Description

Summary

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.

Official Title

A Randomized, Multi-Center, Double-Blind, Phase III Study Evaluating the Efficacy and Safety of Hetrombopag Olamine Tablets Vs Placebo in Patients With Chemotherapy-Induced Thrombocytopenia

Keywords

Patients With Chemotherapy-Induced Thrombocytopenia, Hetrombopag Olamine

Eligibility

You can join if…

Open to people ages 18 years and up

  1. Male or female, age ≥ 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 ≥ 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 ≥6 months.
  9. Signed ICF for voluntary participation in the study and good compliance.

You CAN'T join if...

  1. WHO Grade ≥ 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.

Locations

  • UCLA accepting new patients
    Los Angeles California 90095 United States
  • Cancer and Blood Specialty Clinic accepting new patients
    Los Alamitos California 90254 United States
  • Starling Oncology not yet accepting patients
    Long Beach California 90805 United States

Lead Scientist at University of California Health

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Jiangsu HengRui Medicine Co., Ltd.
ID
NCT07286032
Phase
Phase 3 Chemotherapy-Induced Thrombocytopenia Research Study
Study Type
Interventional
Participants
Expecting 150 study participants
Last Updated