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Could this pill prevent Chemo-Related bleeding risks?

NCT ID NCT07286032

Disease control Sponsor: Jiangsu HengRui Medicine Co., Ltd. Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jul 15, 2026 · Updated 2 times

Summary

This study tests an experimental drug, hetrombopag, to see if it can safely raise platelet counts in cancer patients whose platelets drop too low after chemotherapy. About 150 adults with solid tumors (like lung, breast, or colon cancer) will receive either the drug or a placebo during their chemo cycles. The goal is to help patients complete their planned chemo without delays or needing rescue treatments for low platelets.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 3

Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.

Participants

About 150 people

The number the study aims to enrol. It can still change while the study runs.

Started

Apr 2026

Expected to finish

Jun 2029

An estimate. End dates often move.

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. Male or female gender, 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 21-day treatment cycles. 4. Eastern Cooperative Oncology Group performance status (ECOG PS) 0-2. 5. Life expectancy ≥6 months. 6. Signed ICF for voluntary participation in the study and good compliance. Exclusion Criteria: 1. Hematopoietic diseases other than CIT (e.g., primary immune thrombocytopenia). 2. Hematologic malignancies. 3. 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. 4. Untreated brain metastases; or with leptomeningeal metastasis. 5. Conditions that require emergent treatment (e.g., superior vena cava syndrome, spinal cord compression). 6. Severe cardiovascular disorders or interventions within 6 months 7. Have arterial/venous thrombosis within 6 months 8. Known bleeding disorders, platelet dysfunction 9. Severe haemorrhage during screening 10. Acute or uncontrolled hepatitis B\&C infection 11. Human immunodeficiency virus (HIV) infection.

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Conditions

The condition(s) this trial relates to.

acquired thrombocytopenia chemotherapy-induced toxicity neoplasm

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Patients with chemotherapy-induced thrombocytopenia

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    7 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • AdventHealth Hematology and Oncology Denver Cypress Hematology and Oncology

    NOT_YET_RECRUITING

    Denver, Colorado, 80210, United States

  • Cancer and Blood Specialty Clinic

    NOT_YET_RECRUITING

    Los Alamitos, California, 90254, United States

  • Mid-Florida Hematology & Oncology Centers, P.A.

    RECRUITING

    Orange City, Florida, 32763, United States

  • Morristown Medical Center

    NOT_YET_RECRUITING

    Morristown, New Jersey, 07039, United States

  • New York Cancer and Blood Specialists One Oncology

    NOT_YET_RECRUITING

    Shirley, New York, 11967, United States

  • Oncology & Hematology Associates of West Broward

    NOT_YET_RECRUITING

    Coral Springs, Florida, 33065, United States

  • Springfield Clinic

    NOT_YET_RECRUITING

    Springfield, Illinois, 62702, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.