Phase 1 Oesophageal Cancer Trial, Recruiting NCT07578571 Sponsor: Immunome, Inc. Condition: Oesophageal Cancer
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Phase 1 Oesophageal Cancer Trial, Recruiting

NCT07578571
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:

  • You are generally able to carry out some or all of your usual daily activities (your doctor will have rated your physical fitness on a standard scale as 0, 1, or 2)
  • For the first part of the trial (Part A): You have been diagnosed with an advanced or spread cancer that cannot be removed by surgery, including certain types of colorectal cancer, lung cancer, breast cancer, stomach or esophageal cancer, or possibly other cancer types if approved by the trial team
  • For the second part of the trial (Part B): You have been diagnosed with advanced colorectal cancer, advanced lung cancer, or another specific cancer type depending on which group (cohort) you are being considered for
  • Your cancer is not considered curable and you have already tried standard treatments, could not tolerate them, or they are not suitable for you — with no other standard options remaining
  • For colorectal cancer (Part B): You have already been treated with specific standard chemotherapy drugs and other targeted treatments, or they were not suitable for you
  • For lung cancer (Part B): You have already been treated with standard platinum-based chemotherapy and an immunotherapy drug, or they were not suitable for you
  • Your cancer can be measured on scans according to standard medical guidelines

Who may not be able to join:

  • You have previously received a specific type of cancer drug (called an antibody-drug conjugate) that targets an enzyme called topoisomerase-1 — though people with lung cancer or breast cancer may have had up to one of these treatments
  • You have had a serious allergic reaction (anaphylaxis) to certain chemotherapy drugs such as irinotecan, or to the type of drug being studied
  • Your expected life expectancy is less than 12 weeks (confirm with trial site)
  • You have previously had a solid organ transplant (such as a kidney, liver, or heart transplant)
  • You have a build-up of fluid in your abdomen or around your lungs that is causing symptoms
  • You have active cancer that has spread to your brain or the lining around your brain or spinal cord
  • You have a history of another separate cancer diagnosis, unless you received treatment that may have cured it, you have had no signs of it returning for at least 2 years, and the trial team approves your participation

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 28 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

Phone: 425.939.7410

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
Immunome, Inc.
Registry
ClinicalTrials.gov
Start date
21 May 2026
Est. completion
1 January 2029

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Evaluate the safety and tolerability of IM-1617 in participants with unresectable locally advanced or metastatic solid tumors by incidence of adverse events (AEs) and serious adverse events (SAEs); Evaluate the safety and tolerability of IM-1617 in participants with unresectable locally advanced or metastatic solid tumors by incidence of AEs of interest (AEIs); Evaluate the safety and tolerability of IM-1617 in participants with unresectable locally advanced or metastatic solid tumors by incidence of AEs leading to discontinuation; Evaluate the safety and tolerability of IM-1617 in participant...

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: 28 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