Stomach Cancer Trial, Recruiting NCT06417892 Sponsor: Cancer Institute and Hospital, Chinese Academy of Medical Sciences Condition: Stomach Cancer
Back to Stomach Cancer

Stomach Cancer Trial, Recruiting

NCT06417892
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who have fully understood the study and have voluntarily signed a consent form
  • People aged 18 or older
  • People who have been diagnosed through laboratory testing with advanced stomach cancer or cancer at the junction of the stomach and oesophagus, and who have already had at least one course of treatment for it
  • People who have previously received immune therapy drugs (including PD-1 drugs), either before surgery, after surgery, or as a main treatment — and for people whose cancer spread or came back within 6 months of finishing that treatment, that earlier treatment counts as their first-line treatment
  • People whose general physical fitness is rated 0 or 1 on a standard medical scale, and whose fitness level has not declined in the 7 days before joining
  • People with a Body Mass Index (BMI) of 18 or higher
  • People whose doctors expect them to live for at least 3 months
  • People whose blood, liver, kidney, and heart results fall within the ranges required by the trial (confirm with trial site for exact values)
  • Women who are able to become pregnant and are using effective contraception
  • People who are willing to attend follow-up appointments and cooperate with the study requirements

Who may not be able to join:

  • People who are unlikely or unwilling to follow the study plan and procedures
  • People who have previously been treated with a type of drug that targets a protein called VEGFR
  • People who have previously been treated with paclitaxel (a chemotherapy drug), unless that treatment was given before or after surgery and ended more than 6 months before the cancer got worse
  • People whose cancer tests positive for a marker called HER-2
  • People who have received a live vaccine within 4 weeks before joining, or who may need one during the study
  • People who have had another cancer in the past 5 years, except for certain skin cancers or cervical pre-cancers that were fully treated with surgery
  • People who have an active autoimmune disease, or who had one within the 4 weeks before joining
  • People who have previously had a bone marrow transplant or an organ transplant from another person
  • People who are known to be allergic to the study drug or any of its ingredients
  • People with electrolyte (blood chemical) abnormalities that the doctor considers medically significant
  • People with high blood pressure that cannot be controlled with medication, defined as a top reading of 150 mmHg or higher and/or a bottom reading of 90 mmHg or higher
  • People who have a condition affecting how their body absorbs medication, or who are unable to swallow tablets or capsules
  • People with active stomach or gut conditions such as stomach ulcers, ulcerative colitis, active tumour bleeding, or other conditions the doctor believes could cause gut bleeding or a tear in the gut
  • People with a significant history of bleeding — including more than 30 mL of bleeding in the past 3 months, coughing up blood in the past 4 weeks, or a stroke or mini-stroke in the past 12 months
  • People with significant heart disease, including a heart attack, severe chest pain, or heart bypass surgery in the past 6 months; certain types of heart failure; irregular heart rhythms requiring medication; or a low heart pumping function
  • People with a serious active infection that is not under control
  • People known to have HIV; people with active hepatitis B (confirmed with specific blood test results); or people with active hepatitis C (confirmed with specific blood test results)
  • People who still have side effects from previous cancer treatment that are above a mild level (except for hair loss, low lymphocyte counts, or certain mild nerve side effects from a specific chemotherapy)
  • People who are pregnant or breastfeeding
  • People who have received a blood transfusion, blood products, or certain blood-boosting medicines (such as albumin or G-CSF) within 28 days before joining
  • People with any other medical condition, abnormal test result, or physical finding that the doctor believes would make the study drug unsafe or make it hard to interpret the study results
  • People whose urine tests show a high level of protein (2+ or more on a standard test, confirmed by a 24-hour urine collection showing more than 1.0g of protein)
  • People who the trial doctors consider unsuitable for the study for any other reason

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 27 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: LIN YANG, Doctor, Cancer Institute and Hospital, Chinese Academy of Medical Sciences

Phone: 010-87788145

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Registry
ClinicalTrials.gov
Start date
15 April 2024
Est. completion
31 May 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

PFS

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov