Phase 1 Stomach Cancer Trial, Recruiting NCT05208762 Sponsor: Seagen, a wholly owned subsidiary of Pfizer Condition: Stomach Cancer
Back to Stomach Cancer

Phase 1 Stomach Cancer Trial, Recruiting

NCT05208762
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 one of the following cancer types that has spread or cannot be surgically removed: non-small cell lung cancer, head and neck squamous cell carcinoma (but not nasopharyngeal cancer), esophageal squamous cell carcinoma, triple negative breast cancer, pancreatic cancer, liver cancer (hepatocellular carcinoma), stomach cancer, or endometrial cancer — depending on which part of the trial is involved
  • People whose cancer has come back, stopped responding to standard treatments, or where standard treatments are not suitable or have not been tolerated
  • People who have previously had a test showing their cancer's level of a protein called PD-L1 (confirm with trial site for exact level required, as this varies by cancer type and trial part)
  • People who are generally well enough to carry out daily activities with little or no limitation (this is measured using a standard scale called ECOG, with a score of 0 or 1)
  • People who have at least one area of cancer that can be measured on a scan using standard criteria

Who may not be able to join:

  • People who have had another type of cancer diagnosed within the past 3 years, or who still show signs of a previously diagnosed cancer
  • People with currently active cancer that has spread to the brain (though people whose brain metastases were previously treated may still be considered, if they have been stable for at least 4 weeks, have no new or growing brain spots, and have not needed steroid medication for brain-related symptoms for at least 7 days before starting the trial)
  • People whose cancer has spread to the lining surrounding the brain and spinal cord
  • People who have recently received certain immunotherapy drugs that target PD-L1 (specifically within a timeframe of less than 5 half-lives of that drug)
  • People who have previously been treated with a drug containing a substance called MMAE (monomethylauristatin E)
  • People who already have moderate or severe nerve damage (called neuropathy, grade 2 or higher) before joining the trial

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
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: Pfizer CT.gov Call Center, Pfizer

Phone: 1-800-718-1021

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
Seagen, a wholly owned subsidiary of Pfizer
Registry
ClinicalTrials.gov
Start date
25 October 2022
Est. completion
5 January 2028

Where this trial is recruiting

🇧🇪 Belgium 🇨🇦 Canada 🇨🇳 China 🇫🇷 France 🇩🇪 Germany 🇮🇹 Italy 🇯🇵 Japan 🇳🇱 Netherlands 🇪🇸 Spain 🇬🇧 United Kingdom 🇺🇸 United States

Primary endpoints

Number of participants with adverse events (AEs); Number of participants with laboratory abnormalities; Number of participants with dose-limiting toxicities (DLTs); Number of participants with DLTs by dose level

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