Phase 2 Oesophageal Cancer Trial, Recruiting NCT06975410 Sponsor: Yuhan Corporation Condition: Oesophageal Cancer
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Phase 2 Oesophageal Cancer Trial, Recruiting

NCT06975410
Recruiting Phase 2

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 must be willing and able to sign a consent form before any study procedures begin.
  • You must be generally well enough to carry out daily activities with little or no limitation (this is measured by a standard health scale called ECOG 0 or 1 — confirm with trial site).
  • Your doctors estimate you have a life expectancy of at least 3 months.
  • You must not be breastfeeding.
  • You must have at least one area of disease that can be measured by CT or MRI scan, has not been treated with radiation before, and meets specific size requirements.
  • For the dose escalation part of the trial: You have an advanced or spreading solid tumour that shows high levels of a protein called EGFR (confirmed by a lab test), has not responded to or could not be tolerated on standard treatments, and cannot be cured by local treatment. Eligible tumour types include certain cancers of the head and neck, lung, oesophagus, bile ducts, cervix, vulva, bladder/urinary tract, or skin.
  • For the dose expansion part of the trial (Group 1): You have a confirmed advanced or spreading head and neck cancer (not nasopharyngeal carcinoma) that shows high EGFR levels, has not responded to or could not be tolerated on standard treatments, and cannot be cured by local treatment.

Who may not be able to join:

  • You have uncontrolled cancer that has spread to the brain or spinal cord, or cancer affecting the lining around the brain.
  • You have a history of a second type of cancer, unless it was certain skin cancers or early-stage cancers that were fully treated and cured, or another cancer with no known active disease and no treatment in the last 2 years.
  • You have a history of moderate to severe heart failure (Class II, III, or IV as defined by a standard heart scale — confirm with trial site).
  • You have had a heart attack, heart bypass surgery, unstable chest pain, or a heart stent or similar procedure in the past 24 weeks.
  • You have a history of non-infectious lung inflammation (interstitial lung disease or pneumonitis) that needed steroid treatment, or you currently have this condition.
  • You have an autoimmune disease that has needed treatment affecting your whole body.
  • You are infected with HIV.
  • You have active hepatitis B or hepatitis C.
  • You are currently taking or have recently taken steroid medicines as a systemic treatment (confirm timing with trial site).
  • You have previously been treated with a specific type of immune-activating drug called a 4-1BB/CD137 agent.
  • You have received a live vaccine within the past 4 weeks.
  • You have recently received immunotherapy, biological therapies, targeted drug treatments, or hormonal therapies (confirm timing with trial site).
  • You have recently received radiation therapy (confirm timing with trial site).
  • You have recently received chemotherapy (confirm timing with trial site).

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 2: approximately ~30% 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: Yuhan Clinical Research Physician, Yuhan Corporation

Phone: +82-2-828-0150

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 2
Sponsor
Yuhan Corporation
Registry
ClinicalTrials.gov
Start date
12 June 2025
Est. completion
1 June 2027

Where this trial is recruiting

🇰🇷 South Korea

Primary endpoints

Treatment-emergent adverse events (TEAEs) including dose limiting toxicities (DLTs); Objective Response Rate (ORR)

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