Phase 2 Lung Cancer Trial, Recruiting NCT06249854 Sponsor: Korea Institute of Oriental Medicine Condition: Lung Cancer
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Phase 2 Lung Cancer Trial, Recruiting

NCT06249854
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:

  • People who have given written consent after receiving a full explanation of the trial and choosing to take part voluntarily
  • Adults aged 19 years or older
  • People who have been diagnosed with advanced (stage IV) non-small cell lung cancer, confirmed by laboratory testing of tissue or cell samples; if the cancer has come back, it must have spread to areas outside the chest
  • People whose cancer is planned to be treated with pembrolizumab (an immunotherapy drug) as the first treatment, and whose tumour tests show a PD-L1 score of 50% or higher with no EGFR or ALK gene mutations present
  • People with a life expectancy of at least 3 months
  • People who are reasonably active and able to care for themselves, based on a standard medical scoring system (ECOG score of 0, 1, or 2)
  • People who have at least one measurable area of cancer that can be tracked using standard imaging guidelines
  • People whose blood and organ function test results meet certain minimum levels, including healthy enough levels of red blood cells, white blood cells, and platelets, as well as adequate kidney and liver function (confirm with trial site for specific values)

Who may not be able to join:

  • People who have active cancer that has spread to the brain and is causing noticeable neurological symptoms
  • People who have been diagnosed with another separate cancer in the past 5 years that could affect the lung cancer, with some exceptions for certain previously treated and cured cancers (confirm with trial site)
  • People who have been treated with certain immunotherapy drugs (immune checkpoint inhibitors or anti-CTLA-4 treatments) in the past 6 weeks, or with immune-suppressing medications in the past 2 weeks, with some exceptions for low-dose steroids
  • People currently taking thiazide or loop diuretics (a type of fluid or blood pressure medication)
  • People with low potassium levels in the blood (below 3.0 mEq/L)
  • People with active lung inflammation (interstitial lung disease) that requires steroid treatment taken by mouth or through a drip
  • People with an autoimmune disease that currently requires ongoing medical treatment
  • People with diabetes that is not well controlled despite medication, based on specific blood sugar and HbA1c measurements
  • People with high blood pressure that remains uncontrolled despite taking blood pressure medication
  • People with serious uncontrolled heart conditions, such as severe heart failure, unstable chest pain, or certain irregular heart rhythms
  • People with certain rare inherited conditions affecting how the body processes sugars, such as galactose intolerance or glucose-galactose malabsorption
  • People with a known active or uncontrolled infection with HIV, tuberculosis, hepatitis B, or hepatitis C
  • People who are pregnant or currently breastfeeding
  • People who do not agree to use effective contraception during the trial and for at least 5 months after the last dose of the study treatment
  • People who have taken herbal medicines in the 4 weeks before starting the study treatment, if the trial doctor considers this could affect the trial or the person's safety
  • People who have taken part in another clinical trial and received an experimental drug within 30 days before starting this study treatment
  • People who have had a severe allergic skin reaction to the study treatment or its ingredients (such as rash, hives, or eczema)
  • People who the trial doctor considers unsuitable for any other reason, such as serious infection or organ failure

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 13 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: Sung Yong Lee, Ph.D, Koera University Guro Hospital

Phone: 042-868-9475

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
Korea Institute of Oriental Medicine
Registry
ClinicalTrials.gov
Start date
8 February 2024
Est. completion
31 December 2025

Where this trial is recruiting

🇰🇷 South Korea

Primary endpoints

Progression-Free Survival (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: 13 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