Phase 1 Stomach Cancer Trial, Recruiting NCT07360314 Sponsor: EMD Serono Research & Development Institute, Inc. Condition: Stomach Cancer
Back to Stomach Cancer

Phase 1 Stomach Cancer Trial, Recruiting

NCT07360314
Recruiting Phase 1

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 been diagnosed with an advanced solid tumour (confirmed by laboratory testing of tumour tissue) that has a high level of a protein called Ly6E.
  • People whose tumour cannot be surgically removed and has either spread to other parts of the body or is locally advanced, and has stopped responding to standard treatments, or for whom no suitable standard treatment exists.
  • People with one of these specific cancer types who have already received prior treatments where those treatments are available locally: non-small cell lung cancer, triple-negative breast cancer, squamous cell carcinoma of the head and neck, pancreatic ductal adenocarcinoma, gastric (stomach) cancer, or epithelial ovarian cancer.
  • People who are generally well enough to carry out basic daily activities, as measured by a standard medical scale called the ECOG Performance Status score of 0 or 1 (meaning fully active or restricted in physically strenuous activity but able to carry out light work).
  • People whose blood counts, liver function, and kidney function are within levels considered safe for participation.
  • Other criteria set out in the trial protocol may also apply.

Who may not be able to join:

  • People who have had another type of cancer diagnosed within the past 3 years (some exceptions may apply, such as certain skin cancers, early-stage cervical changes, benign prostate conditions, or cancers considered cured with very low chance of return — the trial team would assess these on a case-by-case basis).
  • People who have previously had a bone marrow or stem cell transplant from a donor.
  • People who have cancer that has spread to the brain, unless all brain tumours have been treated locally and have been stable for at least 4 weeks, and the person has no ongoing neurological symptoms related to the brain disease.
  • People who have had diarrhoea (loose or liquid stools) or a bowel blockage of a certain severity within the week before treatment starts.
  • People who have an active chronic inflammatory bowel condition (such as Crohn's disease or ulcerative colitis) or a bowel obstruction.
  • People who have had a serious gastrointestinal bleed within 3 months before treatment starts.
  • Other exclusion criteria set out in the trial protocol may also apply.

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 8 July 2026
Phase 1: approximately ~10% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Medical Responsible, EMD Serono Research & Development Institute, Inc.

Phone: 888-275-7376

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
Phase 1
Sponsor
EMD Serono Research & Development Institute, Inc.
Registry
ClinicalTrials.gov
Start date
13 February 2026
Est. completion
20 September 2028

Where this trial is recruiting

🇨🇦 Canada 🇯🇵 Japan 🇪🇸 Spain 🇺🇸 United States

Primary endpoints

Dose-escalation Cohort: Occurences of Dose Limiting Toxicities (DLTs); Dose-escalation Cohort: Number of Participants With Treatment-Emergent Adverse Event (TEAEs) and Adverse Event (AEs)

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: 8 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